Pages 2 - 64 focus on vaccine ingredients.
Page 65 discusses medical diagnostic codes for vaccine injuries and what diagnostic codes are.
Contraindication checklist forms that doctors are SUPPOSED to use but rarely do can be found on pages 66-68
An alternative vaccine refusal form to fill out and hand to the doctor when declining vaccines for your child(ren) can be found on page 69-70 (DO NOT FILL OUT THE ONE DOCTORS GIVE YOU)
Vaccine package inserts are on 71- 124 (Vaccines linked to ear infections as stated by their package inserts on 124)
Vaccine related information including scientific studies start on page 125
Pages 200-210 discuss how vaccines trigger an improper immune system response.
Pages 211-212 discusses a primate model study which shows that vaccines cause the amygdala (part of the brain) to not develop properly
Page 213 contains a copy of a Wyeth memo discussing a decision to not put out too many vials of each vaccine lot in one area anymore after there was a cluster of Sudden Infant Death cases as a result of the DPT and DPTH vaccines
"There is no Federal requirement for informed consent relating to immunization." http://www.cdc.gov/vaccines/imz-managers/laws/
This table includes not only vaccine ingredients (e.g., adjuvants and preservatives), but also substances used during the manufacturing process of vaccines (see images on the next four pages or click on link) https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf
Infant amputated foreskins, cancer tissues from human lungs as well as a human cervix, diseased monkey kidney, cancer tissue from a mouse, aborted fetal cells, and diseased canine kidneys were used to grow the viruses for multiple vaccines - http://www.cellprolabs.com/continuous-cell-lines
This link confirms that cell line HFF from the previous link is from infant foreskins https://www.systembio.com/downloads/Manual_HFFn_booklet_WEB.pdf
Infant amputated foreskins were used to help grow the viruses used in the Gardasil and Cervarix HPV vaccines - http://www.nytimes.com/2006/08/29/health/29hpv.html?pagewanted=all&_r=0
Scientist Anthony Samsel has found the following vaccines to be contaminated with Monsanto Glyphosate (Roundup), which the WHO has classified as “probably carcinogenic to humans”: MMR, Varicella (chicken pox), Zostavax (shingles), Proquad (MMR, rubella, varicella), Fluzone Quad (flu vaccine), Hepatitis B (B Energix-B), DTap (diphtheria, tetanus, pertussis) . Click on the following link and also see the following 3 images - http://www.tonu.org/2016/08/31/vaccine-glyphosate-link/
DOWNLOAD THE PUBLISHED STUDY HERE: http://www.amsi.ge/jbpc/11717/25SA16A.pdf
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Glyphosate pathways to modern diseases VI: Prions, amyloidoses and autoimmune neurological diseases
"Using the VAERS database, we have shown that severe adverse reactions to the MMR vaccine have increased significantly over the past decade in step with the increased use of glyphosate. Glyphosate in MMR may originate from growth of the live virus on culture materials derived from glyphosate-exposed animals and/ ...or from gelatin used as an excipient stabilizer. We have confirmed the presence of glyphosate contamination in MMR and in many other vaccines where the live virus is cultured in eggs, bovine protein or gelatin, or where animal products are used as an excipient component. Notably, some vaccines prepared without live culture on gelatin were free of glyphosate contamination. Substitution of glyphosate for glycine during protein synthesis could yield a peptide that resists proteolysis, making it more likely to induce an immune response. Furthermore, enzymes involved in proteolysis are likely to be disrupted due to their confirmed contamination with glyphosate. A non-exhaustive list of possible diseases that can be attributed to this mechanism include autism, multiple sclerosis, type 1 diabetes, coeliac disease, inflammatory bowel disease and neuromyelitis optica"
http://www.amsi.ge/jbpc/11717/25SA16A.pdf
“The proposed mechanism underlying Roundup®-induced neurotoxicity is summarized in Fig. 9. In conclusion, our results showed that the herbicide Roundup® leads to glutamatergic excitotoxicity and energy deficit in hippocampal cells from immature rats. The mechanisms underlying Roundup® neurotoxicity involve activation of kinase cascades as well as misregulation of glutamatergic synapses, Ca2+ influx through NMDA and L-VDCC, energetic deficits and oxidative damage in rat hippocampus. Thus, we propose that Roundup® induced glutamatergic excitotoxicity which culminate in neural cell death.” https://d3n8a8pro7vhmx.cloudfront.net/yesmaam/pages/680/attachments/original/1431795616/GLYPHOSATE_neurotoxicity_induced_by_glyphosate-based_herbicide_in_immature_rat_hippocampus_(1).pdf?1431795616
Vaccine ingredient descriptions and effects
2-Phenoxyethanol- “The major hazards encountered in the use and handling of 2-phenoxyethanol stem from its toxicologic properties. Toxic by all routes (inhalation, ingestion, and dermal contract). Exposure to this faintly aromatic, colorless, oily liquid may occur from its use as a fixative for cosmetics, perfumes and soaps; as a bactericide and insect repellant; as a solvent for cellulose acetate, dyes, stamp pads, ball point, and specialty inks.” (5) “It has the ability to inhibit phagocytic activity, meaning toxic to all cells. The phenol the 2-PE is capable of disabling the immune system's primary response mechanism. It can also cause systemic poisoning, headache, shock, weakness, convulsions, kidney damage, cardiac failure, kidney failure, or death” (6) Included in Polio (IPV), Dtap (Daptacel), Dtap+IPV+Hib (Pentacel), Tdap (adacel)
3-0-desacyl-4' Monophosphoryl lipid- “The invention pertains to adjuvant and vaccine compositions of monophosphoryl lipid A, sugar and optionally an amine based surfactant, which when frozen and thawed or lyophilized and reconstituted reform a colloidal suspension having a light transmission of greater than or equal to 88 % as measured spectrophotometrically.” (7) “Adjuvant System 04 (AS04) consisting of MPL (3-O-desacyl-4′-monophosphoryl lipid A) adsorbed onto a particulate form of aluminum salt is one of these new generation adjuvants now licensed for use in humans” (8) Included in HPV (Cervarix)
A-tocopheryl hydrogen succinate- “A natural tocopherol and one of the most potent antioxidant tocopherols. It exhibits antioxidant activity by virtue of the phenolic hydrogen on the 2H-1-benzopyran-6-ol nucleus. It has four methyl groups on the 6-chromanol nucleus. The natural d form of alpha-tocopherol is more active than its synthetic dl-alpha-tocopherol racemic mixture.” (9) “Vitamin E is the name given to a group of water-insoluble, plant-derived substances. There are eight naturally-occurring isomers and a number of semisynthetic or synthetic homologues. The naturally-occurring d- (or RRR) alpha-tocopherol is the most biologically active form and vitamin E activity is traditionally expressed in terms of equivalents of this isomer (mg alpha-tocopherol equivalents or a-TE). Other tocopherols such as gamma-tocopherol also have vitamin E activity. There are four tocopherol homologues (d-a-, d-ß-, d-?- and d-d-) and four tocotrienols. Other forms of vitamin E occur in lower amounts in foods and are less active in animal bioassay. The usual form in supplements is synthetic dl- (or all-rac) a-tocopherol that consists of a mixture of active and inactive stereoisomers, because natural vitamin E from wheat germ oil is expensive.” (10) Included in Influenza (Flulaval)
Alcohol- “Alcohol is a chemical class as well as a discrete substance name. In chemistry, a hydroxyl group ( -OH ) added to a molecule of carbon structure is called an 'alcohol'. So add an -OH to a benzene ring and get phenol. Drink that and you die quickly. Phenol is really what is used when people think formaldehyde is being used. It is an alcohol but it isn't "alcohol". Alcohol, a term standing alone without something else modifying it means booze - Ethyl alcohol. Eth means two carbons.” “Alcohol is a good chemical defatting agent . Rub it on your hands and see how chafed they get. That last feature is what we use alcohol for. Fat removal. It is used in window cleaning agents for that chemical trait.Nerves come in two main sorts, those with fat envelopes and those without. The fat insulation speeds up the nerve transmission chemistry by insulating it from the general circulating milieu, the part with chloride and sodium and potassium and calcium ions just itching to pour through neural pores. Fat covered nerves conduct faster by controlling that conduction specific milieu and focusing the ion current to receptive nodes.If there is a nerve that, innocent as it may be, is carrying way too much data as inappropriate bursts of spastic overly repetitive pulses, then placing a speed bump on that nerve can reduce the ill of that overactivity.Alcohol injected right on the nerve directly, strips off the fat from that location and slows conduction there. Multiple speeding impulses pile up and come through as one single impulse. So a stream of impulses such as :gogogogogogogogog-----gogogogogogo----- comes through the block area as:
go-----go-----go-----go----- Engineers call this a low pass filter. When a muscle gets hit with a single "go" it responds. When it gets hit with a barrage of gogogogogogogogog it gets thrown into tetany, a rigid hard to undo contractile state. Worse, it screams for help over feed back circuits which (in spasticity) are mistakenly linked into the motor circuits by reflex spinal pathways.” (11) Included in Meninagococcal (MPSV4-Menomune)
Aluminum hydroxide- “Aluminum hydroxide is used for the relief of heartburn, sour stomach, and peptic ulcer pain and to promote the healing of peptic ulcers. Aluminum hydroxide is also used sometimes to decrease the amount of phosphate in the blood of patients with kidney disease. Side effects include constipation, loss of appetite, confusion, unusual tiredness or discomfort, and muscle weakness” (12) Included in Tdap (Boostrix), Dtap (Infranix), Hep B (Engerix-B), HPV (Cerverix), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix), Hep A (Havrix), Hep A+Hep B (Twinrix)
Aluminum hydroxyphosphate sulfate- same as amorphous aluminum hydroxyphosphate sulfate. Included in Hib (PedvaxHIB)
Aluminum phosphate- “Aluminum phosphate mixture is a slow acting antacid used similarly to aluminum hydroxide mixture. Unlike aluminum hydroxide, it does not interfere with phosphate absorption and is used when a high-phosphorus diet cannot be maintained or if there is diarrhea or a deficiency of pancreatic juice. It is also used as an adjuvant in adsorbed vaccines. The mixture is given in doses of 5 to 15 ml and dried aluminum phosphate in doses of 400 to 800 mg. Aluminum is ubiquitous, it is the most abundant metal in the earth's crust. The majority of human exposure comes from food. It is present in some pharmaceuticals, primarily antacids, analgesics, antacids, antidiarrheals, astringents and as adjuvants for vaccines. In industry it is widely used in construction materials and packaging. Aluminum inhibits bone remodeling, causing osteomalacia. It is believed to inhibit erythropoiesis, causing anemia.Acute toxicity is rare. Most cases of aluminum toxicity in humans are in one of two categories: patients with chronic renal failure, or people exposed to aluminum in the workplace. Soluble forms of aluminum (such as aluminum chloride (AlCl(3+)), aluminum fluoride (AlF(3)), aluminum sulfate (Al(SO4)3) and aluminum citrate (AlC(6)H(8)O(7))) have greater potential for toxicity than insoluble forms (such as aluminum hydroxide(AlOH(3))), due to their greater absorption. Patients with renal failure are prone to aluminum toxicity, either from aluminum in the dialysate or other exogenous sources, especially aluminum-containing phosphate binders and antacids. Signs and symptoms may include dementia, memory loss, aphasia, ataxia, seizures, altered EEG, and osteomalacia. Encephalopathy has been reported in patients with renal failure. This may range from mild personality changes and speech disorders to severe obtundation, seizures,coma and death. Fatal encephalopathy with status epilepticus has occurred after the use of aluminum-containing bone cement in vestibular neurectomies. Aluminum has also been linked to the histopathology of Alzheimer disease. Occupational exposure to aluminum has been associated with cognitive deficits and delayed reaction times. Aluminum in drinking water has been linked to central nervous system birth defects. Some aluminum compounds have proven teratogenic in laboratory animals; however, overall, aluminum is not considered teratogenic.” (13) Included in Pneumococcal (PVC13-Prevnar13), Dtap (Daptacel), Dtap+Hep B+IPV (Pediarix), Dtap+IPV+Hib (Pentacel), Hep A+Hep B (Twinrix), Tdap (Adacel)
Amino acids- “An amino acid is any molecule that contains both amino and carborylic acid functional groups. Amino acid is any one of the class of simple organic compounds containing carbon, hydrogen, oxygen, nitrogen, and incertain cases, sulfur. Theses compounds are the building blocks of proteins.” (14) “The side effects of taking too much amino acids depend largely on the kind of amino acid that is being taken. Most are practically harmless and offer many benefits, while others (such as tyrosine) have been reported to cause restlessness, anxiety, and rapid heart beat at higher doses in rare cases.” (15) Included in Hep B (Recombivax), HPV (Cerverix), HPV (Gardasil), Hib+Hep B (Comvax), Hep A (Havrix), Hep A+Hep B (Twinrix), Meningococcal (MCV4-Menveo), Rotavirus (Rotarix)
Ammonium sulfate- “The chemical compound ammonium sulfate is primarily used in fertilizers but is important in other industries as well. While it isn’t considered highly hazardous to humans, there are some important precautions to take if you’re using it. Ammonium sulfate, also called diammonium sulfate or sulfuric acid diammonium salt, is a white crystalline solid with no smell. It tastes salty. The compound dissolves easily in water but will not dissolve in alcohol or acetone. It readily absorbs water, so if it’s exposed to moist air, it will “scab” on the damp surfaces. When ammonium sulfate reacts with alkaline substances, it gives off ammonia gas. Finally, ammonium sulfate is a fertilizer that’s sometimes used in making homemade explosives. Ammonium sulfate is used most commonly as an artificial fertilizer for alkaline soils. When introduced into damp soil, an ammonium ion is released. This creates a small amount of acid, which lowers the pH balance of the soil. It also contributes nitrogen, which aids in plant growth. It dissolves relatively slowly, which makes it cheaper than some other artificial fertilizers. Ammonium sulfate is also used as an herbicide because it will burn the leaves of plants and either kill them outright or at least weaken them for easy removal. This compound is used in the production of printed circuit boards. It’s also in flame retardant materials because it lowers the combustion temperature and increases the production of residues or chars. Ammonium sulfate activates yeast, so it helps to get industrially produced bread to rise, and it’s also a general-purpose food additive. Finally, it plays an important role in developing vaccines during the purification process. The DTap vaccine, which protects children from diphtheria, tetanus, and whooping cough, uses ammonium sulfate for this purpose. Ammonium sulfate is potentially dangerous to both people and the environment, so it requires care in its use. It can cause severe irritation and inflammation of the respiratory tract if inhaled. Eating or drinking ammonium sulfate will cause irritation in the gastrointestinal tract like nausea, vomiting, and diarrhea, although it isn’t toxic unless consumed in large quantities. Contact with the skin or eyes will cause irritation, redness, itching, and pain. It may also be a neurotoxin, meaning it can cause confusion and behavioral changes.” (16) Included in Hib (ActHIB), Pneumococcal (PCV13-Prevnar13), Dtap (Daptacel), Dtap+TPV+Hib (Pentacel), Tdap (Adacel)
Amorphous aluminum hydroxyphosphate sulfate- “Merck Aluminum Adjuvant (AAHS) is a proprietary aluminum hydroxyphosphate sulfate formulation that is both physically and functionally distinct from traditional aluminum phosphate and aluminum hydroxide adjuvants. At a macromolecular level, AAHS is structurally related to aluminum phosphate as it forms an amorphous mesh like structure. AAHS bears a nearly zero charge at neutral pH”(17) “The amount of aluminum in the recommended individual dose of a biological product shall not exceed 1.250mg. However, infants are exceeding the maximum recommended dose depending on which vaccine is given, and how many vaccines are being given in one day. This far exceeds the FDA’s safety limit on aluminum. “The FDA determined that babies should not get more than about 25 to 50 micrograms of aluminum in any one day,” Dr. Sears says. “If too much aluminum is injected all at once, it can find its way into the brain, bones and body organs and cause damage. This was discovered many years ago in hospitalized patients who were receiving IV solutions containing too much aluminum.” Aluminum neurotoxicity has been recognized in experimental animals, in individuals with renal failure, and links to neurodegenerative disorders to aluminum exposure. Also, aluminum content in infant formulas, and in intravenous solutions for home parenteral nutrition, has been associated with neurological consequences and metabolic bone disease, characterized by low-bone formation rate.Symptoms of mild to moderate acute aluminum phosphide toxicity may include nausea, agitation and chills, restlessness, abdominal pain, tightness in chest, and excitement. Symptoms of aluminum toxicity may include disorientation, colic, memory loss, headaches, learning difficulty, mental confusion, heartburn, loss of coordination, and flatulence. More severe symptoms of toxicity may include tachycardia (rapid pulse), diarrhea, respiratory failure, cyanosis, dizziness and/or death, difficulty breathing, pulmonary edema, and hypotension (low blood pressure). Convulsions have been to occur in lab animals exposed to high concentrations of phosphine. Severe exposure may indicate kidney damage. Pathological examination of exposed laboratory animal tissue and results of post-mortem examinations of phosphine poisoning in people generally indicate hypoxia, along with evidence of local trauma in the gastrointestinal tract or lungs, liver, kidneys and central nervous system. The antigen presenting cells can cause problems. Dendritic cells that present antigen for too long will allow abnormal antibodies to be produced; also known as autoantibodies. Antigen presenting cells from vaccines promote a better immune response and aluminum ensures this abnormal response.When macrophages cross the blood brain barrier they take aluminum with them and are thus affected by aluminum as well. They can become loaded with aluminum particles and disrupt their function. Aluminum can integrate into molecular functions but it is also a neurotoxin. It alters permeability of the blood-brain barrier making the brain more accessible to other toxins in the body, just as Thimerosal can. Aluminum hydroxide when used in vaccines is injected through the skin right to the tissue where it is absorbed and enters the brain. Myelin is the protective protein which coats neurons and covers the spinal cord. Damage to this protein is referred to as demyelination. Multiple Sclerosis, Acute Disseminated Encephalomyelitis, Autism, Transverse Myelitis, and Optic Neuritis are examples of demyelinating diseases when damage to myelin causes neurological dysfunction. So, Aluminum interacts directly with DNA. Exogenous aluminum interacts via membrane contact and with cell signaling events. Both mechanisms take place and around 30 genes can be affected. Seven of which are significantly up-regulated or in other words, genes that are primarily pro-inflammatory or pro-apoptotic: apoptosis means cell suicide. The consequences for brain development are still unknown since there has not been enough research done to date. However, it is known that aluminum in vaccines is sufficient to induce abnormal gene expression in the brain. ” (18) Included in Hep A (Vaqta), Hep B (Recombivax), HPV (Gardasil), Hib+Hep B (Comvax)
Arginine- “L-arginine is an amino acid commonly sold in supplement form and obtained naturally in the diet. L-arginine-rich foods include plant and animal proteins, such as dairy products, meat, poultry, fish, and nuts. It may help with health problems such as angina, erectile dysfunction, congestive heart failure, boost immune system, colds, and high blood pressure. There are a number of side effects including indigestion, nausea, headache, bloating, diarrhea, gout, blood abnormalities, allergies, airway inflammation, worsening of asthma, and low blood pressure. Higher doses can increase stomach acid, so it may also worsen heartburn, ulcers, or digestive upset caused my medication. Due to safety concerns, L-arginine should be avoided by diabetes patients, people who have suffered heart attack and pregnant or nursing women” (19)
Beta-propiolactone- “beta-Propiolactone is used for vaccines, tissue grafts, surgical instruments, and enzymes, as a sterilant of blood plasma, water, milk, and nutrient broth, and as a vapor-phase disinfectant in enclosed spaces. Acute (short-term) inhalation exposure to beta-propiolactone causes severe irritation of the eyes, nose, throat, and respiratory tract in humans. Acute dermal exposure may cause irritation of the skin, blistering, or burns in humans. Contact with the eyes may cause permanent corneal opacification. Burns of the mouth and stomach may occur in humans following acute exposure via ingestion. No information is available on the chronic (long-term), reproductive, developmental, or carcinogenic effects of beta-propiolactone in humans. Squamous cell carcinomas of the forestomach have been reported in orally exposed rats. In dermally exposed rodents, skin tumors have been observed. The International Agency for Research on Cancer (IARC) has classified beta-propiolactone as a Group 2B, possible human carcinogen. Acute inhalation exposure beta-propiolactone causes severe irritation of the eyes, nose, throat, and respiratory tract in humans. Acute dermal exposure may cause irritation of the skin, blistering, or burns in humans. Contact with the eyes may cause permanent corneal opacification. Burns of the mouth and stomach may occur in humans following acute exposure via ingestion. Acute oral exposure has been observed to result in muscular spasms, respiratory difficulty, and convulsions at high levels in rats. In rats acutely exposed intravenously, liver and kidney tubular damage has been reported. In mice, hamsters, and guinea pigs dermally exposed, skin tumors have been observed. EPA has not classifiedbeta-propiolactone for carcinogenicity. IARC has classified beta-propiolactone as a Group 2B, possible human carcinogen.” (20) Included in Influenza (Fluvirin)
Bovine albumin (bovine extract)- “Bovine serum albumin (BSA) is commonly used in cell culture protocols, particularly where protein supplementation is necessary and the other components of serum are unwanted. In cell culture, its main role is as a carrier of small molecules. Because of its negative charge, Bovine Serum Albumin binds water, salts, fatty acids, vitamins and hormones, then carries these bound components between tissues and cells.” (21) When the BSA is attached to an antibody, the complex may deposit in the membrane of the kidney. This leads to inflammation and breakdown of the filter membrane barrier, allowing it to leak imoprtant bodily proteins, clotting factors, immune globulins, etc. that normally would be held back in the selective filteration process. Some diseases that are “nephrotic” include idopatic membranous nephropathy, minimal charge nephropathy (most common in children). Protein-losing nephropathies like theses result in several other problems in the body, namly high blood pressure, high cholesterol and kidney insufficiency. They can also lead to clotting disorders from loss of anitithrombin, infections die to loss of important immune globuins, and vitamin D deficiency due to loss of vitamin D binding proteins among other things. (22) Included in Hep A (Vaqta), Dtap+IPV+Hib (Pentacel), Dtap (Infrarix), Tdap (Boostrix), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix)
Calcium carbonate- “Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. Side effects include upset stomach, vomiting, stomach pain, belching, constipation, dry mouth, increased urination, decreased appetite, metallic taste.” (23) “Calcium carbonate, or CaCO3, comprises more than 4% of the earth’s crust and is found throughout the world. Its most common natural forms are chalk, limestone, and marble, produced by the sedimentation of the shells of small fossilized snails, shellfish, and coral over millions of years. Although all three forms are identical in chemical terms, they differ in many other respects, including purity, whiteness, thickness and homogeneity. Calcium carbonate is one of the most useful and versatile materials known to man.” (24) Included in Rotavirus (Rotarix)
Calf Serum Protein (fetal bovine serum)- “Serum is the liquid fraction of clotted blood from fetal calf, depleted of cells, fibrin and clotting factors, but containing a large number of nutritional and macromolecular factors essential for cell growth. Bovine serum albumin is the major component of the fetal bovine serum. Very important is the myriad of growth factors in fetal bovine serum, which are essential for the maintenance and growth of cultured cells. Fetal bovine serum also contains small molecules like amino acids, sugars, lipids, and hormones. FBS is used in cell culture of eukaryotic cells, and has a wide range of applications. For example, it’s used in the research, manufacture, and control of human and veterinary vaccines and of biotech drugs.” (25) For more information about extraction and effects on the human body see fetal bovin serum. Included in Polio (IPV-Ipol), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix), MMRV (ProQuad), Zoster (Shingles-Zostavax), Rotavirus (RotaTaq), Varicella (Varivax)
Carbohydrates- “Carbohydrates are one of the three macronutrients in our diet (fat and protein being the others). They exist in many forms and are mainly found in starchy foods such as bread, pasta, and rice, as well as in some beverages, e.g. fruit juices and sugar-sweetened drinks. Carbohydrates represent the most important source of energy for the body, and are vital for a varied and balanced diet. The building blocks of all carbohydrates are sugars and they can be classified according to how many sugar units are combined in one molecule. Glucose, fructose and galactose are prominent examples among the single unit sugars, also known as monosaccharides. Double units are called disaccharides, with sucrose (table sugar) and lactose (milk sugar) being the most widely known.” (26) Included in HPV (Gardasil)
Casamino acids- “Amino acid mixture obtained through the hydrolysis of caseine and used in bacteriology as a culture medium” (27) “Casein is a protein that is found in milk and used independently in many foods as a binding agent. Technically, it is part of a group called phosphoproteins, collections of proteins bound to something containing phosphoric acid. It may also be called caseinogen, particularly in European foods. Casein has also been linked to negative effects in people with autism. While in most people, this protein is easily broken down by the digestive system into peptides known as casomorphins, and then further processed into basic amino acids, some evidence suggests that in autistics, this process does not occur fully. The resulting casomorphins, which fail to break down completely, may have an effect on the body similar to that of morphine or other opiates. For this reason, some experts on autism recommend that people suffering from autism avoid products containing this protein.” (28) Included in Pneumococcal (PCV13-Prevnar13)
Cell culture media- “Animal or plant cells, removed from tissues, will continue to grow if supplied with the appropriate nutrients and conditions. When carried out in a laboratory, the process is called Cell Culture. It occurs in vitro (‘in glass’) as opposed to in vivo (‘in life’). The culture process allows single cells to act as independent units, much like a microorganism such as a bacterium or fungus. The cells are capable of dividing, they increase in size and, in a batch culture, can continue to grow until limited by some culture variable such as nutrient depletion.Cultures normally contain cells of one type although mixed cultures, especially of bacteria, are common in food sciences and wastewater treatment related studies. The cells in culture may be genetically identical (homogenous population) or may show some genetic variation (heterogeneous population). A homogenous population of cells derived from a single parental cell is called a clone. Therefore all cells within a clonal population are genetically identical.” (29) Included in Rotavirus (RotaTeq)
Chick embryo cell culture (egg protein)- “The paper below shows that vaccines cultured in chick embryos (such as measles and mumps) contain "retroviruses" that show potential for replicating (and causing cancer) in the host (human). Researchers have detected "reverse transcriptase" activity in vaccines. Reverse transcriptase is a DNA polymerase enzyme that transcribes single-stranded RNA into double-stranded DNA. 'BACKGROUND: A recent publication reporting the presence of low levels of reverse transcriptase (RT) activity in certain vaccines for human use necessitated that regulatory agencies address the issue of whether this RT activity presented a risk to humans. Detection of low levels of RT activity corresponding to fewer than ten virions became possible with the development of highly-sensitive polymerase chain reaction (PCR)-based RT (PBRT) assays. Variations of the PBRT assay were developed in three laboratories. These assays were reported as being at least one million-fold more sensitive than conventional RT assays. OBJECTIVE: To ascertain the sensitivity and reliability of PBRT assays in different laboratories and to determine which vaccine samples possessed RT activity. STUDY DESIGN: Coded panels of licensed vaccines together with positive and negative controls was assembled at the Center for Biologics Evaluation and Research (CBER) of the Food and Drug Administration (FDA) and distributed to five cooperating laboratories as well as to our laboratory at CBER. Each laboratory carried out their version of the PBRT assay and submitted the results to the coordinator at CBER. RESULTS: Results of the PBRT analyses carried out in the six laboratories are presented. Five of the six laboratories reported results that were highly consistent. RT activity was detected in live attenuated vaccines that were prepared in chick embryo cells (mumps, measles and yellow fever), but very low or undetectable RT activity was found in vaccines produced in mammalian cells (rabies and rubella). influenza vaccines from several manufacturers included in the panel displayed the most variability, with different products of this inactivated vaccine having differing amounts of RT activity. CONCLUSIONS: Only vaccines produced in chick embryo cells had significant RT activity. Because RT activity was present in the allantoic fluid of uninfected chick embryos and culture medium from chick embryo fibroblasts, the RT activity arises from the cell substrate used for vaccine production. The PBRT assays were reliably able to detect the low levels of RT activity in chicken-derived vaccines.' -Maudru T, Peden KW. Laboratory of Retrovirus Research, Food and Drug Administration, Bethesda, MD 20892, USA. Analysis of a coded panel of licensed vaccines by polymerase chain reaction-based reverse transcriptase assays: a collaborative study.Clin Virol. 1998 Jul 24;11(1):19-28.” (30) Included in MMR (MMRII), MMRV (ProQuad), Influenza (Fluvirin), Influenza (Flumist), Influenza (Fluzone:high dose)
CMRL 1969 medium (supplemented with calf serum)- “An improved tissue culture basal medium, CMRL-1969, supplemented with serum, has been evaluated by measuring the growth responses of primary cultures of trypsin-dispersed monkey kidney cells (PMKC) and of an established culture of a human diploid cell strain (HDCS). Medium H597, an early modification of medium 199 which has been used successfully in the preparation of poliomyelitis vaccine for 15 years, was used for comparison. In addition, parallel testing was done with Basal Medium Eagle (BME) widely used for the growth of HDCS. The improvements in basal medium CMRL-1969 are attributed to changes in amino acid concentrations, in vitamin composition, and, in particular, to enhanced buffering capacity. The latter has been achieved by the use of free-base amino acids and by increasing the dibasic sodium phosphate.” (31) For more information see calf serum, monkey kindey cells, and human dipliod cells. Included in Dtap+IPV+Hib (Pentacel)
Complex fermentation medium- “Yeast extract (YE) is commonly used as a key component in the complex media for industrial fermentations. However, the lot-to-lot variation of this raw material frequently requires extensive "use testing" of many lots to identify only the few that support desired fermentation performance. Through extensive fermentation studies and chemical analyses, we have identified adenine and two metabolizable carbon sources, trehalose and lactate, as the principle components in YE that affect the production of a recombinant protein antigen by a yeast strain. Adenine is required for culture growth and the relationship between biomass and measured adenine can be expressed by a Michaelis-Menten model, while the slowly metabolized trehalose serves to maintain the energy supply to the continued antigen synthesis. The rapidly utilized lactate exerts an indirect positive effect by sparing some of the accumulated ethanol from being consumed for growth to being utilized in the product formation. The effects of these YE components are mutually dependent. Based on the database generated from 40 lots at laboratory scale, a relatively high level of carbon sources in YE (trehalose plus lactate, >9.5% w/w) and an intermediate level of adenine (0.14-0.24% w/w) appear to be the minimal requirement of a good lot for this recombinant yeast fermentation. Many poor lots were improved in lab fermenters by rational supplementation of trehalose, lactate, or adenine to compensate for their insufficiencies. At the large production scale, predictions based on adenine and trehalose/lactate contents in various YE lots used correlated reasonably well with culture growth and antigen yield, illustrating the feasibility of such a simple chemical/biochemical analysis as a rapid and reliable initial screening tool. Without incurring any compositional change to an established manufacturing medium, this study demonstrates an effective approach to achieve consistency in fermentations employing complex nutrients and to improve fermentation productivities supported by suboptimal lots of raw material.” (32) Included in Hib (PedvaxHIB)
CY medium- “Casitone.....................5.0 g
Yeast extract................1.0 g
Distilled water..............1.0 L (33)
For more information see yeast. Included in Meningococcal (MCV4-Menveo)
Detergent- There are many different detergents used in vaccines. Some examples are Trinton X-100 or octylphenol ethorylate, sodium deoxycholate, polysorbate 20, sodium taurochenodeoxycholate. (34) “Cytotoxic; detergents cause cells to leak or explode by weakening their walls. This catastrophically mimics the membrane attack complex (MAC) Octoxynol 9 (or 10) and Triton X-100 typically contain traces of the toxicants ethylene oxide, dioxane, C9 phenols, or glycol ether. Sodium Deoxycholate causes cell death and symptoms such as burning, redness, and swelling. It has been shown to weaken the blood-brain-barrier (BBB) and subsequently activate seizures. It is also known to promote tumor growth. It demonstrates synergistic toxicity -- notably with Amphotericin B, the antifungal listed above. Sodium Taurodeoxycholate has been observed to promote tumor growth in the throat, pancreas, colon and other tissues. By increasing cell permeability it also increases drug uptake showing that exposed cells become more vulnerable to toxic insult.” (35)(36)(37)(38)(39) Included in Hib (PedavaxHIB), Hib+Hep B (Comvax), Influenza (Fluzone:high dose), Meninagococcal (MPSV4-Menomune), Influenza (Fluvirin), Influenza (Flulaval), Hep B+Hep A (Twinrix)
Dextran- “The physical and chemical properties of purified dextrans vary depending on the microbial strains from which they are produced and by the production method. Dextrans have high water solubility and the solutions behave as Newtonian fluids. Solution viscosity depends on concentration, temperature, and molecular weight, which have a characteristic distribution. The hydroxyl groups present in dextran offer many sites for derivatization, and these functionalized glycoconjugates represent a largely unexplored class of biocompatible and environmentally safe compounds.”(40) Included in Rotavirus (Rotarix)
Dextrose- “Dextrose is the commercial name used for the crystalline glucose produced from starch. If the crystallized dextrose (glucose) contains no water, it is listed as “dextrose anhydrous” or “anhydrous dextrose” in an ingredient statement. If the crystallized dextrose contains one molecule of water, it will be listed as “dextrose” or “dextrose monohydrate” in an ingredient statement. The majority of the dextrose listed in food ingredient statements began as cornstarch. Food manufacturers may list dextrose produced from cornstarch as “corn sugar” in an ingredient statement. If the dextrose comes from another source like rice or wheat, the ingredient list would read “rice sugar” or “wheat sugar,” respectively. Dextrose is used in many baking products like cake mixes and frostings, snack foods like cookies, crackers and pretzels, and desserts like custards and sherbets. Dextrose is also used as a filler in the single-serve, table-top packets of the common artificial sweeteners.” (41) “When used in small doses, no common side effects have been reported with this product. Seek medical attention right away if any of these severe side effects occur while taking glucose (the active ingredient contained in Dextrose) Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).” (42) Included in Hib+Hep B (Comvax), Hep B (Recombivax)
Dibasic potassium phosphate- “Dipotassium Phosphate is a stable chemical compound used in various manufactured products (mostly food). It comes as an odorless, white crystal powder with a shelf life of about 12 months. It is deliquescent when exposed to moist air. Used as additive in the coffee creamers substitute and as nutrient in various powdered materials (stabilizer (emulsifier) in non-dairy creamers, bodybuilding drinks). Its function is to prevent protein coagulation, and also to prevent its precipitation. It is a humectant. Also included in foods where low Sodium is specified, like low Sodium cheeses. It helps control the pH in food processing applications. Used as nutrient in microorganism cultures to produce antibiotics, and as a buffering agent in certain pharmaceuticals. Put into antifreeze solutions as a buffer and sequestrate, used as a dispersion medium in liquid detergents and as an additive in cheese processes. It's an ingredient in non-toxic antifreeze. Used as a high efficient, compound fertilizer preparation for special purposes and as additive in the paper industry.” (43) “As well as its needed effects, potassium phosphate may cause unwanted side effects that require medical attention. Side effects include burning, crawling, itching, numbness, prickling, "pins and needles", or tingling feelings, chest pain or discomfort, confusion, dizziness, faintness, or lightheadedness when getting up suddenly from a lying or sitting position, fast, slow, or irregular heartbeat, muscle cramps in the hands, arms, feet, legs, or face, no muscle tone or movement, numbness and tingling around the mouth, fingertips, or feet, pounding or rapid pulse, shortness of breath, unusual tiredness or weakness, weakness and heaviness of the legs” (44) Included in Influenza (Flumist), MMRV (ProQuad)
Dimethyl-1-beta-cyclodextrin- “Cyclic structure oligomers of glucose ( called cyclodextrins) are obtained from the starch digests of the bacteria Bacillus macerans. The individual glucose units are connected by 1,4 bonds. The most abundant cyclodextrins are alpha, beta and gamma cyclodextrin which have 6,7 and 8 glucose units respectively. The interior cavity is hydrophobic and the outside of the molecule is hydrophilic. The enhanced of characteristics such as stability, aqueous solubility, and reduced volatility, can be modified through propoxylation reactions of them. Potential applications of cyclodextrins include water-soluble pharmaceuticals, prolonged drug release, tabletting and herbicides and pesticides.” (45) “CDs offer an additional tool for the formulator to overcome some of the formulation and delivery limitations of problematic drugs. As with any new tool, they have both strengths and weaknesses. Their major strengths are the specific nature of how they interact with drug molecules and their ability to deliver safely a number of intractable drug molecules. The specific nature of their interaction is also a weakness in that only molecules with the right size, geometry, and intrinsic solubility properties benefit from their use. Whereas both α-CD and β-CD and a number of alkylated CDs are known to be renally toxic and disruptive of biological membranes, γ-CD and some of its derivatives, as well as HP-β-CD and SBE-β-CD, appear to be much safer. As more products using CDs are approved or undergo evaluation by regulatory agencies for use in food and pharmaceuticals, concerns about their safety will be clarified.” (46) “Mitochondrion-based MTT test was a more sensitive indicator of cytotoxicity than the plasma membrane-based propidium iodide test.” (47) “The products of the bvgAS locus coordinately regulate expression of the Bordetella pertussis virulence regulon in response to environmental signals. Transcription of bvgAS-activated genes is nearly eliminated by several modulating conditions, including the presence of sulfate anion or nicotinic acid and growth at low temperature. We have isolated spontaneous mutations that result in the constitutive synthesis of multiple bvg-regulated loci. Several of these mutations have been analyzed and were found to result from single-nucleotide substitutions within bvgS, in a region encoding a 161-amino-acid segment which links the transmembrane sequence with cytoplasmic domains that appear to be involved in signaling events. The effect of signal transduction mutations in Escherichia coli was determined by measuring the expression of an fhaB-lacZYA transcriptional fusion, and that in B. pertussis was determined by measuring expression of both fhaB-cat and ptxA3201-cat fusions. The constitutive mutations have little effect on fhaB-cat or fhaB-lacZYA expression in the absence of modulating signals but result in a nearly complete insensitivity to MgSO4, nicotinic acid, or growth at low temperature. Furthermore, insertion and deletion mutations in bvgS sequences encoding the periplasmic domain eliminate activity of the wild-type product, whereas constitutive mutants remain active. In B. pertussis cultures grown in Stainer-Scholte broth, expression of ptxA3201-cat differed from that of fhaB-cat in several respects. In combination with a wild-type bvgS allele, ptxA3201-cat expression required the addition of heptakis-(2,6-O-dimethyl)-beta-cyclodextrin, and this requirement was eliminated by the presence of the constitutive mutations.” (48) Included in Dtap (Daptacel), Tdap- (Adacel)
Dulbercco's modified Eagle medium (DMEM)- There are many different additives that go into different formulas of this medium. “The most basic formulation offered. This formulation is used by investigators who want to start with the essential components of DME, and have the flexibility to optimize the formula for their own application. Powder, Without L-glutamine, glucose, phenol red, sodium pyruvate and sodium bicarbonate, Supplement with 0.584 gm/L of L-glutamine; 1.0 gm/L glucose; 3.7 gm/L of sodium bicarbonate, Formulated at 8.3 grams of powder per liter of medium , Cell culture tested. Liquid form of the original Dulbecco's formulation, offered as D 5523, with one key exception. Pyridoxal, which is an aldehyde, has been replaced with pyridoxine. This modification has been shown to improve the stability of the medium. Liquid, With 1000 mg/L glucose and sodium bicarbonate, Without L-glutamine, With pyridoxine (substitutes pyridoxine HCl for pyridoxal Hcl), cell culture tested, endotoxin tested, sterile-filtered.” (49) Included in Rotavirus (Rotarix)
Eagle MEM modified medium- Minimum Essential Medium (MEM) is a modification of Basal Medium Eagle (BME). It was developed by Harry Eagle to meet the specific nutritional requirements of certain subtypes of HeLa cells and normal mammalian fibroblasts. MEM includes higher concentration of amino acids so as to closely approximate the protein composition of cultured mammalian cells.
Composition :
Ingredients mg/L
INORGANIC SALTS
Calcium chloride dihydrate 265.000
Magnesium sulphate anhydrous 97.720
Potassium chloride 400.000
Sodium bicarbonate 2200.000
Sodium chloride 6800.000
Sodium dihydrogen phosphate anhydrous 122.000
AMINO ACIDS
L-Arginine hydrochloride 126.000
L-Cystine dihydrochloride 31.300
L-Histidine hydrochloride monohydrate 42.000
L-Isoleucine 52.000
L-Leucine 52.000
L-Lysine hydrochloride 72.500
L-Methionine 15.000
L-Phenylalanine 32.000
L-Threonine 48.000
L-Tryptophan 10.000
L-Tyrosine disodium salt 51.900
L-Valine 46.000
VITAMINS
Choline chloride 1.000
D-Ca-Pantothenate 1.000
Folic acid 1.000
Nicotinamide 1.000
Pyridoxal hydrochloride 1.000
Riboflavin 0.100
Thiamine hydrochloride 1.000
i-Inositol 2.000
OTHERS
D-Glucose 1000.000
Phenol red sodium salt 11.000 (50) Included in Polio (IPV-Ipol)
Egg proteins- “Egg allergy is one of the most common food allergies of childhood, with a prevalence of 1% to 3% in children under 3 years of age. It is often associated with eczema in infants and asthma in young children. As most children outgrow their egg allergy, the prevalence in adulthood is much lower and is estimated at 0.1%. The most common egg allergy is to egg white. Cross-sensitivity with egg yolk and chicken protein has been described. Vaccines that contain small quantities of egg protein can cause hypersensitivity reactions in some people with allergies to eggs. In Canada, there are several vaccines manufactured by processes involving hens’ eggs or their derivatives, such as chick cell cultures.” (51) For more information see chick embryo cell culture. Included in Incluenza (Fluvirin), Influenza (Flumist), Influenza (Fluzone: high dose), MMR (MMRII), MMRV (ProQuad)
Enzymes- “Enzymes are proteins that initiate change. The enzymes found in the human body are naturally occurring. They catalyze, or accelerate, all normal biochemical reactions in the body. Enzymes are responsible for all metabolic functions and many are absolutely vital for life itself. These proteins are highly specific regarding what they do and under what conditions they do it. Like a glove and a hand, the enzyme and substrate must fit correctly in order to work.” (70) Included in Hib (PedvaxHIB), Hib+Hep B (Comvax)
Ethanol- “Ethanol is a grain alcohol that can be blended with gasoline and used in motor vehicles. Many gasoline stations provide a blended fuel, which typically is 10 percent ethanol and 90 percent gasoline. Ethanol can be fermented from many sources of starch, including corn, wheat, grain sorghum, barley, and potatoes, and from sugar crops such as sugar cane and sweet sorghum. Because there has been has been an abundant supply of corn, most of the ethanol made in the United States is from corn.” (71) For effects on the body see alcohol description. Included in Hib (PedvaxHIB), Hib+Hep B (Comvax)
Ethylenediamine tetraacetic acid (EDTA)- “Chelation therapy is a treatment that involves repeated intravenous (IV) administration of a chemical solution of ethylenediaminetetraacetic acid, or EDTA. It is used to treat acute and chronic lead poisoning by pulling toxins (including heavy metals such as lead, cadmium, and mercury) from the bloodstream. The word chelate comes from the Greek root chele, which means "to claw." EDTA has a claw like molecular structure that binds to heavy metals and other toxins.” (52) “EDTA is a chemical that binds and holds on to (chelates) minerals and metals such as chromium, iron, lead, mercury, copper, aluminum, nickel, zinc, calcium, cobalt, manganese, and magnesium. When they are bound, they can't have any effects on the body and they are removed from the body. EDTA is safe when used as a prescription medicine, as eye drops, and in small amounts as a preservative in foods. EDTA can cause abdominal cramps, nausea, vomiting, diarrhea, headache, low blood pressure, skin problems, and fever. It is unsafe to use more than 3 grams of EDTA per day, or to take it longer than 5 to 7 days. Too much can cause kidney damage, dangerously low calcium levels, and death. Nebulizer solutions containing disodium EDTA as a preservative can cause the breathing tubes to narrow in some people with asthma. The size of the dose determines the amount of the narrowing. EDTA might make heart rhythm problems worse. It might interfere with blood sugar control because it can interact with insulin. It can decrease serum calcium levels, making hypocalcemia worse. It can bind with potassium and increase the amount of potassium that is flushed out in the urine. This might cause potassium levels to drop too low, especially in people who have low levels to begin with. If you have this problem, don’t use EDTA. It can bind with magnesium and increase the amount of magnesium that is flushed out in the urine. This might cause magnesium levels to drop too low, especially in people who have low levels to begin with. If you have this problem, don’t use EDTA. EDTA might make liver disease worse. Avoid using EDTA if you have a liver condition. EDTA can harm the kidney and might make kidney disease worse. EDTA doses should be reduced in patients with kidney disease. Avoid using EDTA if you have severe kidney disease or kidney failure.There is some concern that EDTA might increase the risk of seizure in people with epilepsy or in people who tend to have seizures.It can cause severe decreases in blood levels of calcium, and this can cause a seizure. Tuberculosis is a lung infection that is caused by particular bacteria. Sometimes the body is able to “wall off” pockets of infection, making the infection inactive. The bacteria remain alive behind the wall of scar tissue, but they can’t get out to cause illness or infect other people. This scar tissue frequently contains calcium. There is some concern that EDTA might be able to bind the calcium in the scar tissue, causing the “walls” to give way and release bacteria. Don’t use EDTA if you have active TB or had TB in the past.” (53) Included in Influenza (Flumist), Varicalla (Varivax)
Fenton medium (containing a bovine extract)- Fenton medium is well hidden. No inserts or ingredients list. All I could find is that it contains bovine extract. For more information see discription of fetal bovine serum. Included in Dtap (Infanrix), Tdap (Boostrix), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix)
Fetal bovine serum- “After slaughter and bleeding of the cow at an abattoir, the mother's uterus containing the calf fetus is removed during the evisceration process (removal of the mother's internal organs) and transferred to the blood collection room. A needle is then inserted between the fetus's ribs directly into its heart and the blood is vacuumed into a sterile collection bag. This process is aimed at minimizing the risk of contamination of the serum with micro-organisms from the fetus and its environment. Only fetuses over the age of three months are used otherwise the heart is considered too small to puncture. Once collected, the blood is allowed to clot at room temperature and the serum separated through a process known as refrigerated centrifugation. It remains questionable as to whether or not fetuses have already died from anoxia (deprivation of oxygen) prior to serum collection. Nevertheless, no anesthesia is given, despite their possible ability to experience pain and discomfort. Serum is a major source of viral contaminants which once present, are almost impossible to remove from cultures. It can contain viruses, prions (a protein that can transform into a rogue agent) and mycoplasma (considered to be a primitive form of bacteria),each of which can skew the outcome of scientific experiments. Many substances present in FCS have not yet been identified, and of the substances which have been, the function of the cultured cells is not always clear. Serum can suppress cell spreading, attachment and embryonal tissue differentiation, which is the process by which embryonic cells develop into specialized cells for particular functions. Critically, this can actually prevent an objective of cell growth research especially when we talk about growing new organs and limbs.” (54) Nearly 100% of all commercially available fetal bovine serum is contaminated with viruses, there are no clean cultures. The viruses that are known to be contained are bovine diarrhea virus, bovine leukiema virus, bovine immunosuppressive virus, bovine herpes virus and mycoplasma. Mycoplasma causes changes in cell growth characteristics, inhibition of cell growth metabolism, disruption of nucleic acid synthesis, chromosomal aberrations, altered transfection rates and virus susceptibility. Dr. Charles Engel stated at an NIH meeting on Feb. 7th, 2000: “I am now of the view that the probable cause of chronic fatigue syndrome and fibromyalgia is the mycoplasma...” (55) Included in Rotavirus (RotaTeq), Varicella (Varivax), Dtap+IPV (Kinrix), MMRV (ProQuad), Zoster (Shingles-Zostavax), Polio (IPV-Ipol)
Formaldehyde- “Formaldehyde is a commonly used chemical compound that exists in various forms and at room temperature, is a colorless, distinctive, strong and even pungent smelling, flammable and gaseous substance. Formaldehyde has been used in a number of industries for various purposes such as: for the manufacturing of building materials – like pressed wood products (mostly as an adhesive resin), fiber board, plywood, cigarette smoke, fuel burning appliances and kerosene space heaters. Additional uses in household products include: additive for permanent –press, an ingredient in glues, and as a preservative in medical laboratories – as embalming fluid, and as a sterilizer. Since Formaldehyde is a by-product of combustion and other inherent processes, it can be found in significant concentrations and in various environments. It is also critical to note that the “11th report on carcinogens” classifies formaldehyde as "reasonably anticipated to be a human carcinogen". In recent years, the health effects associated with elevated levels of exposure have brought to light the dangers from prolonged and repeated contact with chemical. The major exposure risks associated with formaldehyde come from occupants inhaling contaminated air. Exposure to elevated levels of this substance should be avoided whenever possible as exposures to high levels of formaldehyde can trigger asthma attacks, nausea, watery and/or burning eyes, difficulty breathing, headaches, respiratory irritation, sensitization. Formaldehyde has been shown to cause cancer in animals and according to the Department of Health and Human Services (DHHS), formaldehyde may “reasonably be anticipated to be a carcinogen”.” (56)
“Formaldehyde has been classified as a known human carcinogen (cancer-causing substance) by the International Agency for Research on Cancer and as a probable human carcinogen by the U.S. Environmental Protection Agency. Research studies of workers exposed to formaldehyde have suggested an association between formaldehyde exposure and several cancers, including nasopharyngeal cancer and leukemia.” (57) “Formaldehyde ingestion results in severe corrosive damage to the gastrointestinal tract followed by CNS depression, myocardial depression, circulatory collapse, metabolic acidosis and multiple organ failure. The toxic effects of formaldehyde in experimental animals include irritation, cytotoxicity, and cell proliferation in the upper respiratory tract, ocular irritation, pulmonary hyperreactivity, bronchoconstriction, gastrointestinal irritation, and skin sensitization. Other reported effects include oxidative stress, neurotoxicity, neurobehavioral effects, immunotoxicity, testicular toxicity, and decreased liver, thyroid gland, and testis weights” (58)
Included in Dtap (Infanrix), Hep A (Vaqta), Influenza (Flulaval), Meningococcal (MCV4-Menactra), Polio (IPV-Ipol), Tdap (Boostrix), Hep B (Recombivax), Tdap (Adacel), Dtap (Daptacel), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix), Dtap+IPV+Hib (Pentacel), Hib (Hiberix), Hib+Hep B (Comvax), Influenza (Fluzone: high dose), Meningococcal (MCV4-Menveo)
Formalin- “Formalin is a solution in water of the gas formaldehyde (CH2O). A saturated solution contains about 40% by volume — or 37% by weight — of the gas, plus a small amount of a stabilizer, usually 10-12% methanol; this prevents polymerization. The liquid is used as an embalming fluid and for the preservation of animal specimens and tissue samples. It is also used, generally in a much more dilute form, as a disinfectant, and antibacterial wash and in aquariums for treating parasitic infections in fish. The disinfectant properties of the solution are due to the presence of formaldehyde, which also gives it a pungent, irritating smell. There are a number of hazards associated with the use of formalin. It readily releases formaldehyde gas, which is both toxic and highly flammable. Accidental spillage of the solution can quickly raise the concentration of this gas to dangerous levels, posing a direct threat to health and the risk of fire or explosion. If swallowed, the solution has a corrosive effect on the mouth, tongue and esophagus, causing pain, vomiting and bleeding. Other symptoms include kidney failure, effects on the central nervous system and coma. The lethal dose for humans may be around 1 oz (30 ml). People are more likely to suffer ill effects through inhalation of the vapor. At low levels, it is irritating to the eyes and nose and can cause headaches. At higher levels, inhalation can lead to bronchitis and accumulation of fluid in the lungs. Contact with the skin may cause irritation or dermatitis. Eye contact with very dilute solutions causes irritation, but higher concentrations may damage the cornea and cause loss of vision.” (59) “The results of this investigation may be summarized as follows:
1. The inhalation of formaldehyde gas in even small quantities is followed by bronchitis and pneumonia. Pneumonia is due to the inhalation of the gas and not to secondary infection.
2. Formalin belongs to that rare group of poisons which are capable of producing death suddenly when swallowed.
3. The introduction of formalin into the stomach is followed by the production of a gastritis which varies greatly in character. The duodenum and upper jejunum may also be involved in the inflammatory process.
4. Intraperitoneal injections of formalin cause peritonitis of a fibrino-haemorrhagic character. A definite reaction is obtained when very dilute formalin (1–1000) is employed. In the peritoneal cavity formalin exercises a destructive action upon all organs (pancreas, liver, peritoneal fat, Fallopian tubes, etc.) with which it comes in contact and causes inflammation in these organs.
5. The lethal dose of formalin when injected intraperitoneally into guinea pigs is approximately 2 cc. of 1–1000 formalin for each 100 grm. of body weight.
6. The injection of formalin into the lungs is followed by pneumonia and bronchitis.
7. The inflammation which follows subcutaneous injections of formalin is characterized by intense exudation.
8. The injection of formalin into the muscles produces myositis.
9. The injection of formalin into the anterior chamber of the eye causes the accumulation of an exudate containing leucocytes and fibrin. When formalin is dropped into the conjunctival sac iritis follows and may be severe enough to destroy the eye.
10. Formalin in whatever way introduced into the body is absorbed, and is then capable of producing lesions in the parenchymatous organs.
11. Changes in the liver after absorption of formalin consist of mild or severe grade of cloudy swelling accompanied by vacuolation of the protoplasm, changes in the nuclei and leucocytic infiltration. Focal necrosis may result. Similar changes follow the inhalation of formaldehyde.
12. The injection of formalin or the inhalation of the vapors of formaldehyde produces cloudy swelling of the parenchyma of the kidney. Focal necrosis may result.
13. Pneumonia and bronchitis are found in all animals after the injection of formalin.
14. The leucocytic infiltration which follows the introduction of formalin into an organ has these general characteristics: The eosinophiles are the first leukocytes to appear; these are followed by the other polynuclear leucocytes; last appear the large and small mononuclear leucocytes. Similar phenomena occur in the trachea, bronchi and lungs of animals subjected to formaldehyde inhalations.
15. Formalin is, directly or indirectly, chemotactic for leucocytes. The tissues which are not infiltrated with leucocytes after the injection of formalin are those which have been so injured by the chemical that an inflammatory reaction is impossible.
- Animals subjected to chronic poisoning with formalin administered by intraperitoneal injection develop fibrinous peritonitis, associated with marked eosinophilia. The changes in the kidneys and liver consist of cloudy swelling, fatty degeneration, focal necrosis and leucocytic infiltration.” (60) Included in Hib (ActHIB), Hep A (Havrix), Hep A+ Hep B (Twinrix), Dtap (Infarnix)
Franz complete medium- “The invention relates to a medium for culturing pathogenic bacteria to produce an immunogenic factor. The medium comprises non-animal derived proteinaceous material. The invention also relates to the use of the medium to cultivate pathogenic bacteria, obtaining immunogenic factors from the bacteria being cultivated and preparing vaccines using the immunogenic factors. Culture medium with yeast or soybean extract as amino acid source and no protein complexes of animal origin.” (61) For more information see yeast protein and/or soy protein. Included in Meningococcal (MCV4-Menveo)
Gelatin- “Gelatin is a protein obtained by boiling skin, tendons, ligaments, and/or bones with water. It is usually obtained from cows or pigs. Gelatin is used in shampoos, face masks, and other cosmetics; as a thickener for fruit gelatins and puddings (such as Jell-O); in candies, marshmallows, cakes, ice cream, and yogurts; on photographic film; and in vitamins as a coating and as capsules, and it is sometimes used to assist in “clearing” wines. Gelatin is not vegan.” (62) “Gelatin is likely safe for most people in food amounts and possibly safe in the larger amounts used as medicine. There's some evidence that gelatin in doses up to 10 grams daily can be safely used for up to 6 months. Gelatin can cause an unpleasant taste, sensation of heaviness in the stomach, bloating, heartburn, and belching. Gelatin can cause allergic reactions in some people. There is some concern about the safety of gelatin because it comes from animal sources. Some people are worried that unsafe manufacturing practices might lead to contamination of gelatin products with diseased animal tissues including those that might transmit mad cow disease (bovine spongiform encephalopathy). Although this risk seems to be low, many experts advise against using animal-derived supplements like gelatin.” (63) Included in Varicella (Varivax), Influenza (Fluzone: highdose)
Gentamicin Sulfate- “This medication is used to prevent or treat a wide variety of bacterial infections. Gentamicin belongs to a class of drugs known as aminoglycoside antibiotics. It works by stopping the growth of bacteria. Nausea, vomiting, stomach upset, or loss of appetite may occur. Pain/ irritation/ redness at the injection site may infrequently occur. This medication may rarely cause a severe intestinal condition (Clostridium difficile-associated diarrhea) due to a type of resistant bacteria. This condition may occur during treatment or weeks to months after treatment has stopped. Gentamicin may cause live bacterial vaccines (such as typhoid vaccine) not to work as well. Therefore, do not have any immunizations/vaccinations while using this medication without the consent of your doctor.” (64) Included in Influenza (Flumist)
Glutamate- “Prolonged excitation is toxic to nerve cells. Neurobiologists recognize that the nerve cell messenger, glutamate, can cause harm when its messages are overwhelming. Normally glutamate is swiftly cleared from the nerve cell junctions to keep the messages brief. Molecules called transporters aid in keeping glutamate in proper concentrations around nerve cells. Abundant evidence points to glutamate as a destructive factor in ALS and investigators are working to find out how this can be changed. Gene therapy approaches are under investigation to deliver glutamate transporters to cells affected by ALS. Other avenues towards control of glutamate in ALS are also under active investigation. Nerve cells pass signals to each other and to their target organs by releasing messenger molecules, called transmitters. Many are simple amino acids such as the one called glutamate.
The message is intended to tell the recipient neuron whether to fire off its own neurotransmitters. As with all neurotransmitters, glutamate docks at specific recognition molecules on the receiving neuron. Glutamate is then swiftly cleared from the nerve cell junctions to keep the message brief. Prolonged excitation is toxic to nerve cells, and neurobiologists recognize that glutamate can cause harm when the messages are overwhelming, as in stroke or epilepsy. Glutamate’s toxicity is apparently due to calcium flooding the cell. Calcium is supposed to briefly enter the neuron with each signal and triggers the cell to fire off its own signals and adjust its own activities accordingly. But prolonged calcium inside the cell evidently can do damage, and will even activate programmed cell death.” (65) Included in Varicella (Varivax)
Glutaraldehyde- “Glutaraldehyde is a colorless glass-like crystal that is usually in a 2% to 50% water solution. It is used for cold sterilization of dental and medical equipment and as a preservative, biocide, hardener, and tanning agent. Glutaraldehyde is on the Right to Know Hazardous Substance List because it is cited by ACGIH, DOT and NIOSH. Glutaraldehyde can affect you when inhaled and by passing through the skin. Contact with the liquid and vapor can severely irritate and burn the skin and eyes. Inhaling Glutaraldehyde can irritate the nose, throat and lungs causing coughing, wheezing and/or shortness of breath. Glutaraldehyde can cause headache, nausea and vomiting. Glutaraldehyde may cause a skin allergy and an asthma- like allergy.” (66) “Glutaraldehyde is a hazardous chemical used for cold sterilization of medical and dental equipment. Glutaraldehyde based products are effective sterilants and disinfectants for medical devices that cannot be steam sterilized, are particularly heat-sensitive, for lensed instruments that are commonly subjected to high-level disinfection between patient uses. It is a colorless, oily liquid with a pungent odor. As a cold sterilizer it is commonly used as a 2%-4% aqueous solution, and it is found in Ultizyme. Glutaraldehyde has also been used as a preservative in chemical products such as fabric softeners, antiperspirants and fixatives for biological specimens.” (67) Included in Dtap (Daptacel), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix), Dtap+IPV+Hib (Pentacel), Tdap (Adacel), Tdap (Boostrix)
Hemin Chloride- “Treating symptoms of certain blood disorders (porphyria). It may also be used for other conditions as determined by your doctor. Hemin is an enzyme inhibitor made from red blood cells. It works by correcting certain types of heme deficiency in the liver. May cause mild fever; pain, redness, or swelling at the injection site. Seek medical attention right away if any of these severe side effects occur: Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); change in the amount of urine; unusual bleeding; unusual tiredness.” (68) “Hemin chloride, a heme oxygenase 1 inducer, is a porphyrin complex that is derived from erythrocytes. At a concentration of 20 mM Hemin chloride demonstrated the significance of heme in myotube maturation by increasing size, number, cross-striations, and contraction frequency and strength of myotubes. The compound has been observed to induce cGMP formation through induction of guanylate cyclase. Hemin chloride has been noted to stimulate calcium-dependent K+ channels and modulate fluid transport and Na+ in the loop of henle in rat studies. Hemin has also been documented to give rise to active chloride secretion in Caco-2 cells. In cadmium injured rat testes, hemin chloride demonstrated anti-apoptotic, anti inflammatory and antioxidant properties. Derived from procine.” (69) Included in Hib+Hep B(Comvax)
Human albumin- “Treating a variety of conditions, including shock due to blood loss in the body, burns, low protein levels due to surgery or liver failure, and as an additional medicine in bypass surgery. It may be used for certain conditions as determined by your doctor. Albumin (human) is a concentrate of plasma proteins from human blood. It works by increasing plasma volume or serum albumin levels. Side effects include:Anaphylactoid reactions, fever, chills, rash, nausea, vomiting, tachycardia, hypotension. Dermatologic side effects have included urticaria, skin rash, pruritus, edema, and erythema.Nervous system side effects have included headache, chills, and febrile reactions. Cardiovascular side effects have included hypotension. Gastrointestinal side effects have included nausea, vomiting and increased salivation. Respiratory side effects have included bronchospasm.” (72) Included in MMRV (ProQuad) MMR (MMR-II)
Human diploid cell cultures- “In fact, some vaccines are grown in cell cultures that were originally obtained from two human fetuses. In addition, the rubella virus used to make rubella vaccine was isolated from a third human fetus. Two different strains of human diploid cell cultures made from fetuses have been used extensively for vaccine production for decades. One was developed in the United States in 1961 (called WI-38) and the other in the United Kingdom in 1966 (called MRC-5). WI-38 came from lung cells from a female fetus of 3-months gestation and MRC-5 was developed from lung cells from a 14-week-old male fetus. Both fetuses were intentionally aborted, but neither was aborted for the purpose of obtaining diploid cells. The fetal tissues that eventually became WI-38 and the MRC-5 cell cultures were removed from fetuses that were dead. The cellular biologists who made the cell cultures did not induce the abortions. These two cell strains have been growing under laboratory conditions for more than 35 years.” (73) For more information on effects on the body see WI-38 and MRC-5 descriptions. Included in Varicella (Varivax), Dtap+IPV+Hib (Pentacel), Hep A+Hep B (Twinrix), Hep A (Havrix), MMRV (ProQuad), Zoster (Shingles-Zostavax), Hep A (Vaqta), MMR (MMR-II)
Hydrolyzed gelatin (hydrolyzed collagen)- “Hydrolyzed collagen refers to enzymatically or chemically processed collagen derived from marine life, though it can also be taken from bovine, ox, pig skin, and bone. It is water soluble and contains peptides like amino acids as well as glycine, proline, hydroxyproline, and glutamic acid. Hydrolyzed collagen is normally used to benefit nails and skin due to the presence of the amino acids. It is also used to regenerate cells for the body’s lean muscle mass, benefit arthritis, and even help the body burn off fat and enhance weight loss. Hydrolyzed collagen side effects from topical use may trigger dermatitis or inflammation of the skin. Initially, a mild rash may develop. Since dermatitis is an allergic reaction, the reaction may therefore depend on the person using the cream and doesn’t affect every user. Before taking any supplement orally, you should check with your physician for any allergies to animal products. While marine collagen is very much safe, people might have allergic reactions to animal or plant hydrolyzed collagen. Some hydrolyzed collagen supplements are now being made from chicken. While no studies yet show any bad effects from chicken based hydrolyzed collagen, other chicken based supplements aside from collagen have been known to cause mild cases of nausea, heartburn, diarrhea, constipation, drowsiness, skin reactions, and headache.” (74) For more information see gelatin description. Included in MMR (MMR-II), MMRV (ProQuad)
Hydrolyzed porcine gelatin- Gelatin made from pork. For more information see gelatin or hydrolyzed gelatin. Included in Influenza (Flumist), Zoster (Shingles-Zostavax)
Insect cell and viral proteins- “Insect cells (IC) and particularly lepidopteran cells are an attractive alternative to mammalian cells for biomanufacturing. Insect cell culture, coupled with the lytic expression capacity of baculovirus expression vector systems (BEVS), constitutes a powerful platform, IC-BEVS, for the abundant and versatile formation of heterologous gene products, including proteins, vaccines and vectors for gene therapy. Such products can be manufactured on a large scale thanks to the development of efficient and scalable production processes involving the integration of a cell growth stage and a stage of cell infection with the recombinant baculovirus vector. Insect cells can produce multimeric proteins functionally equivalent to the natural ones and engineered vectors can be used for efficient expression. Insect cells can be cultivated easily in serum- and protein-free media.” (75) “Insect cell culture is a common choice for heterologous protein expression. For large scale production or basic research, insect cells are able to express large quantities of protein with complex post-translational modifications.” (76) “Sf9 (Cat. no. B825-01) and Sf21 (Cat. no. B821-01) cell lines are the traditional cell lines used with baculovirus and originated at the USDA Insect Pathology Laboratory. The cell lines are also suitable for use in the InsectSelect™ System. These two cell lines originated from the IPLBSF-21 cell line, derived from the pupal ovarian tissue of the fall armyworm, Spodoptera frugiperda (O'Reilly et al., 1992; Vaughn et al., 1977). When working with recombinant or wild-type viral stocks (e.g.,infecting cells),
always maintain separate media bottles for cell culture and for virus work. Baculovirus particles can survive and be maintained in media at 4°C, and will contaminate your stock cultures if introduced to culture plates or flasks during passaging. The following section summarizes the most common problems associated with insect cell culture. Morphological changes in the cells or changes in the growth rate can indicate an underlying problem with the culture. Keeping a good record of cells (i.e. ,cell density, viability, and detailed notes on the health of the cells) will help in troubleshooting potential problems that may arise. Information below may be used as a guideline to help troubleshoot common problems observed in culturing insect cells.” (77) “Baculoviruses are arthropod‐specific, enveloped viruses with circular, supercoiled double‐stranded DNA genomes. They infect Lepidoptera (butterflies and moths), Hymenoptera (sawflies) and Diptera (mosquitoes).. While many viruses are studied because of their damaging effects, the study of baculoviruses was stimulated by their potential utility to control insect pests. Later, the utility of baculovirus as gene expression vectors was evidenced and a new research area emerged. A major step forward was the development of bacmid technology (the construction of bacterial artificial chromosomes containing the genome of the baculovirus) which allows the manipulation of the baculovirus genome in bacteria. With this technology, foreign genes can be introduced into the bacmid by site‐ directed recombination or by transposition. Baculoviruses have been used to explore fundamental questions in molecular biology such as the nature of programmed cell‐death. Moreover, the ability of baculoviruses to transduce mammalian cells led to the consideration of their use as gene therapy and vaccine vectors. Strategies for genetic engineering of baculoviruses have been developed to meet the requirements of new application areas, and the establishment of new genetic modification systems is still necessary when an unexplored experimental system is to be addressed. The aim of this chapter is to detail the areas of application of the baculovirus in basic molecular biology and applied biotechnology and the strategies used to generate genetically modified baculoviruses according to each area of study.” (78) “A new vaccine for influenza has hit the market, and it is the first ever to contain genetically-modified (GM) proteins derived from insect cells. According to reports, the U.S. Food and Drug Administration (FDA) recently approved the vaccine, known as Flublok, which contains recombinant DNA technology and an insect virus known as baculovirus that is purported to help facilitate the more rapid production of vaccines.
According to Flublok’s package insert, the vaccine is trivalent, which means it contains GM proteins from three different flu strains. The vaccine’s manufacturer, Protein Sciences Corporation (PSC), explains that Flublok is produced by extracting cells from the fall armyworm, a type of caterpillar, and genetically altering them to produce large amounts of hemagglutinin, a flu virus protein that enables the flu virus itself to enter the body quickly. So rather than have to produce vaccines the “traditional” way using egg cultures, vaccine manufacturers will now have the ability to rapidly produce large batches of flu virus protein using GMOs, which is sure to increase profits for the vaccine industry. But it is also sure to lead to all sorts of serious side effects, including the deadly nerve disease Guillain-Barre Syndrome (GSB), which is listed on the shot as a potential side effect.
“If Guillain-Barre Syndrome (GBS) has occurred within six weeks of receipt of a prior influenza vaccine, the decision to give Flublock should be based on careful consideration of the potential benefits and risks,” explains a section of the vaccine’s literature entitled “Warnings and Precautions.” Other potential side effects include allergic reactions, respiratory infections, headaches, fatigue, altered immunocompetence, rhinorrhea, and myalgia. According to clinical data provided by PSC in Flublok’s package insert, two study participants actually died during trials of the vaccine. But the company still insists Flublok is safe and effective, and that it is about 45 percent effective against all strains of influenza in circulation, rather than just one or two strains.” (79) Included in HPV (Cervarix) and Influenza (Flublock)
L-Histidine- “Histidine is an amino acid. Amino acids are the building blocks of protein in our bodies. People use histidine as medicine. Histidine is used for rheumatoid arthritis, allergic diseases, ulcers, and anemia caused by kidney failure or kidney dialysis. Histidine is involved in a wide range of metabolic processes in the body. Histidine might be safe for most people. Doses of up to 4 grams per day have been used in research without causing noticeable side effects. Not enough is known about the use of histidine during pregnancy and breastfeeding. Stay on the safe side and avoid use.” (80) Included in HPV (Gardasil)
Lactalbumin hydrolysate- “Lactalbumin Hydrolysate (LAH) Solution Concentrate (50X) is a peptone frequently utilized as a nutritional supplement for preparing bacterial, insect and mammalian cell culture, especially as a rich source of amino acids. Lactalbumin Hydrolysate (LAH) is a supplement utilized with Grace's Insect Cell Culture Medium for Baculovirus protein expression systems to assist in increasing biomass production. It is also an overlay for the protein expression. LAH may also be utilized, aside from other cell or tissue culture or microbiological applications/formulations, for the production of vaccines of viral origin.” (81) For more information see insect cells. Included in Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix)
Lactose- “Lactose or milk sugar occurs in the milk of mammals - 4-6% in cow's milk and 5-8% in human milk. It is also a by product in the the manufacture of cheese. The galactose and glucose units are joined by an acetal oxygen bridge in the beta orientation. Lactose intolerance is the inability to digest significant amounts of lactose, the predominant sugar of milk. This inability results from a shortage of the enzyme lactase, which is normally produced by the cells that line the small intestine. Lactase breaks down the lactose, milk sugar, into glucose and galactose that can then be absorbed into the bloodstream. When there is not enough lactase to digest the amount of lactose consumed, produce some uncomfortable symptoms. Some adults have low levels of lactase. This leads to lactose intolerance. The ingested lactose is not absorbed in the small intestine, but instead is fermented by bacteria in the large intestine, producing uncomfortable volumes of carbon dioxide gas. While not all persons deficient in lactase have symptoms, those who do are considered to be lactose intolerant. Common symptoms include nausea, cramps, bloating, gas, and diarrhea, which begin about 30 minutes to 2 hours after eating or drinking foods containing lactose. The severity of symptoms varies depending on the amount of lactose each individual can tolerate.” (82) Included in Hib (Hiberix), Meningococcal (MPSV4-Menomune)
Latham medium (derived from bovine casein)- “Composition of the Modified Latham Medium (per 1 liter of the medium):
Polypeptone 20 g
Bovine heart extract 10 g
Glucose 8.0 g
Sodium chloride 2.5 g
Magnesium sulfate (heptahydrate) 0.1 g
Cystine 0.125 μg
Calcium pantothenate 1.0 mg
Uracil 1.25 mg
Nicotinic acid 0.25 mg
Thiamine 0.25 mg
Riboflavin 0.25 mg
Pyridoxine 0.25 mg
Biotin 2.5 μg
Vitamin B12 0.05 μg
Folic acid 100 μg
Iron(III) chloride (hexahydrate) 32 mg
Iron sulfate (heptahydrate) 0.2 g
(The pH was adjusted to 7.0 using 7N NaOH)” (83) Included in Dtap (Infanrix), Tdap (Boostrix), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix)
Lipids- “All Lipids are hydrophobic: that’s the one property they have in common. This group of molecules includes fats and oils, waxes, phospholipids, steroids (like cholesterol), and some other related compounds.” (84) Included in HPV (Cervarix)
Medium 199- “Medium 199 was originally developed for nutritional studies of chick embryo fibroblasts. It has broad species applicability, particularly for cultivation of non-transformed cells. Medium 199 is widely used in virology, vaccine production, and in vitro cultivation of primary explants of mouse pancreatic epithelium, and rat lens tissues. The complete formulation is available.
Compared to other basal media, Medium 199 contains unique components, including adenine, adenosine, hypoxanthine, thymine, and additional vitamins. Medium 199 is available with Earle's salts for use in a CO2 incubator, or with Hank's salts for use without CO2.” (85) Included in Dtap+IPV+Hib (Pentacel), MMR (MMR-II)
Mineral salts- “Mineral salts are necessary for the correct functioning of the human body. In particular, they are a source of cations, trace elements often present in very small quantities in the body, but which are essential to cell activity. They are involved in tissue formation (organs, muscles, etc.), hormone synthesis, protecting the body, enzyme systems, osmotic balance of body fluids
The body is not capable of synthesizing these minerals. The necessary intake is acquired naturally through the foods that we eat. If this does not happen (due to foods lacking in trace elements, deficiency or poor assimilation) medicinal intake is effective for avoiding some complications or illnesses.” (86) Included in Hep B (Recombivax), HPV (Cervarix), HPV (Gardasil), Hib+Hep B (Comvax)
Minimum essential medium- “Minimum Essential Medium (MEM), developed by Harry Eagle, is one of the most widely used of all synthetic cell culture media. Early attempts to cultivate normal mammalian fibroblasts and certain subtypes of HeLa cells revealed that they had specific nutritional requirements that could not be met by Eagle's Basal Medium (BME). Subsequent studies using these and other cells in culture indicated that additions to BME could be made to aid growth of a wider variety of fastidious cells. MEM, which incorporates these modifications, includes higher concentrations of amino acids so that the medium more closely approximates the protein composition of mammalian cells. MEM has been used for cultivation of a wide variety of cells grown in monolayers. Optional supplementation of non-essential amino acids to the formulations that incorporate either Hanks' or Eagles' salts has broadened the usefulness of this medium. The formulation has been further modified by optional elimination of calcium to permit the growth of cells in suspension.” (87)Included in MMR (MMR-II)
Modified Mueller and Miller medium- “The procedure involves the use of a variant and somewhat unstable strain of Clostridium Tetani and a culture medium containing a pancreatic digest of casein with additional cysteine and tyrosine, beef heart infusion, glucose and inorganic salts. A high concentration of iron must be provided. The “modified” makes it more stable. Casein is a milk protein. Cystine and tyrosine are amino acids. Glucose is the sugar that cells burn. “Pancreatic digest” means that enzymes from the pancreas of an animal are used to break down the soup so the tetanus bacterium can eat it. A basic medium constituted as follows served this purpose: Pancreatic digest of casein, 150.0mg; glucose, 75.0mg; cysteine, 1.25mg; tyrosine, 2.5mg; NaCl, 25.0mg; Na2HPO4, 5.0mg; KH2PO4, 1.75mg; MgSO4.7H20, 0.5mg; reduced iron powder, 2.5 to 5.0mg; H2O to 10 ml.” (88) Included in Hib (ActHIB), Meningococcal (MCV4-Menactra), Dtap (Daptacel), Dtap+IPV+Hib (Pentacel), Tdap(Adacel)
Modified Mueller’s growth medium- same as modified Mueller and Miller medium. Included in Dtap (Daptacel), Dtap+IPV+Hib (Pentacel), Tdap (Adacel)
Modified Stainer- Scholte liquid medium- “ A simple chemically defined medium for the production of phase 1 Bordetella Pertussis described consisting of sodium glutamate, proline, cystine, salts, and growth factors, which is suitable for the large-scale production of phase 1 bordetella pertussis. The cultures were detoxified by the addition of 0.14% formalin.” (89) “The acellular pertussis antigens (PT, FHA, and pertactin) are isolated from Bordetella pertussis culture grown in modified Stainer-Scholte liquid medium. PT and FHA are isolated from the fermentation broth; pertactin is extracted from the cells by heat treatment and flocculation. The antigens are purified in successive chromatographic and precipitation steps. PT is detoxified using glutaraldehyde and formaldehyde. FHA and pertactin are treated with formaldehyde. Each antigen is individually adsorbed onto aluminum hydroxide. Each 0.5-mL dose is formulated to contain 5 Lf of tetanus toxoid, 2.5 Lf of diphtheria toxoid, 8 mcg of inactivated PT, 8 mcg of FHA, and 2.5 mcg of pertactin (69 kiloDalton outer membrane protein).” (90) For more information on effects on the body see formaldehyde and glutaraldehyde. Included in Dtap (Infanrix), Tdap (Boostrix), Dtap (Daptacel), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix), Dtap+IPV+Hib (Pentacel), Tdap (Adacel)
Monkey kidney cells (vero cells)- Monkey kidney cells come from African Green monkeys. They are known to contain SV40 (simian virus 40) which is a monkey virus that grows in monkey tissue (particularly kidneys). In two separate studies there were reports of SV40 in non-Hodgkin's lymphoma tumors. It is used in polio and rotavirus vaccines. (91) “The Vero epithelial cell line was established in 1962 by Y. Yasumura and Y. Kawakita at the Chiba University in Chiba, Japan. The tissue from which the line was derived was obtained from the kidney of a healthy adult African green monkey. Although widely used in transfections and vaccine production, Vero cells are also often utilized in the detection of verotoxins, a group of interrelated toxins produced by some strains of Escherichia coli that are a key cause of hemorrhagic colitic and hemolytic uremic syndrome in humans. The array of viruses that Vero cells are susceptible to is broad and includes polioviruses, simian virus 5 (SV5), simian virus 40 (SV40), rubeola, rubella virus, reoviruses, simian adenoviruses, Getah, Ndumu, Pixuna, Ross River, Semliki Forest, Paramaribo, Kokobera, Modoc, Murutucu, Germiston, Guaroa, Pongola, and Tacaribe. The Vero cell line is negative, however, for reverse transcriptase and is resistant to Stratford, Apeu, Caraparu, Madrid, Nepuyo, and Ossa viruses.” (92) “The polyomavirus simian virus 40 (SV40) is a known oncogenic DNA virus which induces primary brain and bone cancers, malignant mesothelioma, and lymphomas in laboratory animals. Persuasive evidence now indicates that SV40 is causing infections in humans today and represents an emerging pathogen. A meta-analysis of molecular, pathological, and clinical data from 1,793 cancer patients indicates that there is a significant excess risk of SV40 associated with human primary brain cancers, primary bone cancers, malignant mesothelioma, and non-Hodgkin's lymphoma.” (93) Included in Polio (IPV-Ipol), Rotavirus (RotaTeq), Dtap+IPV (Kinrix), Dtap+Hep B+ IPV (Pediarix)
Monobasic potassium phosphate- “The molecular formula of potassium phosphate monobasic is KH2PO4. Potassium phosphate monobasic is a white, odourless, granular or crystalline powder, or colourless crystals. It is freely soluble in water and practically insoluble in alcohol. Apart from its essential role in bone structure, phosphate is also important in many metabolic and enzymatic pathways. It is involved in energy storage and transfer, the utilization of B-complex vitamins, the buffering of body fluids, and in the renal excretion of hydrogen ions. Adverse reactions include Cardiovascular problems including hypotension (uncommon) and myocardial infarction (rare). The following events have been reported but are uncommon: Fluid retention as indicated by swelling of
feet or lower legs or weight gain. Hyperkalaemia leading to confusion, tiredness or weakness, irregular or slow heart rate, numbness or tingling around lips, hands or feet, unexplained anxiety, weakness or heaviness of legs, shortness of breath or troubled breathing. Hyponatremia leading to confusion, tiredness or weakness, convulsions, oliguria or decreased frequency of micturition, tachycardia, headache or dizziness, increased thirst. Hyperphosphataemia, hypocalcaemia or hypomagnesaemia leading to convulsions, muscle cramps, numbness, tingling, pain or weakness in hands or feet, shortness of breath or troubled breathing, tremor. Extraskeletal calcification as nephrocalcinosis has been reported in children with hypophosphataemic rickets treated with phosphate supplements. Rare: acute renal failure” (94) Included in Influenza (Flumist), MMRV (ProQuad), Zoster (Shingles-Zostavax)
Monosodium L-glutamate (MSG)- “MSG, or monosodium glutamate, is a food additive that is used as a flavor enhancer primarily in Asian cooking although it is commonly found in many processed foods. MSG comes from glutamic acid that is naturally found in mushrooms, fermented soy products such as soy sauce and parmesan cheese. Glutamic acid is part of a large category of glutamates which ultimately make up the fifth taste category of umami. Many people find that consuming MSG, especially in larger quantities, can cause negative side effects that can include dizziness, headaches, nausea, flushing, irregular or rapid heartbeats, excessive sweating, intense thirst, skin rash, fatigue or lethargy, numbness, ringing in the ears, and tingling of mouth.” (95) “That’s because the effects of MSG are cumulative. Just because you don’t react to MSG now, doesn’t mean you won’t later. According to Dr. Russell Blaylock, who wrote a book on the subject called Excitotoxins: The Taste That Kills, sensitivity to MSG builds up in our bodies until we reach what he calls our “threshold of sensitivity.” That’s because MSG overstimulates our nervous system — exciting our nerves and causing an inflammatory response. With time, these repetitive inflammatory responses cause our nerves to start producing more and more nerve cells that are sensitive to this kind of stimulation. The more overly-sensitive nerve cells we have, the stronger our immediate response to MSG will be. Way back in 1957, a team researchers decided to see if glutamate could help repair a diseased retina. Remember, glutamate is a common and necessary amino acid in our diet (arguably the most common neurotransmitter in the brain), so this presupposition isn’t so far fetched. The researchers fed rats MSG and were shocked by their results.
Rather than repairing the disease, the MSG destroyed the retinal cells that allow vision! A decade later, the neuroscientist Dr. John Olney used their method of destroying retinal cells so that he could study visual pathways to the brain. He found that MSG not only destroyed retinal vision cells, but also parts of the brain. This brain damage was done as neurons became over excited, virtually exciting themselves to death. He called this “excitotoxicity,” and that has led subsequent researchers to describe MSG as an “excitotoxin.” While the naturally occurring glutamates in food aren’t dangerous, processed free glutamic acids like MSG are. Not only do they cause brain damage and lead to nervous disorders, but they also cause radical hormone fluctuations. Mice injected with MSG become rapidly obese, inactive, and have other hormonal issues.” (96) Included in Influenza (Flumist), Varicella (Varivax), MMRV (ProQuad), Zoster (Shingles- Zostavax)
MRC-5 cells (human diploid) (residual components including DNA and protein)- “The MRC-5 cell line is commonly utilized in vaccine development, as a transfection host in virology research, and for in vitro cytotoxicity testing. Initiated in September 1966 by J. P. Jacobs, the cell line was derived from the human lung tissue of a 14-week-old male fetus aborted from a 27-year-old woman.” (97) “Ratajczak also looks at a factor that hasn't been widely discussed: human DNA contained in vaccines. That's right, human DNA. Ratajczak reports that about the same time vaccine makers took most thimerosal out of most vaccines (with the exception of flu shots which still widely contain thimerosal), they began making some vaccines using human tissue. Ratajczak says human tissue is currently used in 23 vaccines. She discusses the increase in autism incidences corresponding with the introduction of human DNA to MMR vaccine, and suggests the two could be linked. Ratajczak also says an additional increased spike in autism occurred in 1995 when chicken pox vaccine was grown in human fetal tissue. Why could human DNA potentially cause brain damage? The way Ratajczak explained it to me: "Because it's human DNA and recipients are humans, there's homologous recombinaltion tiniker. That DNA is incorporated into the host DNA. Now it's changed, altered self and body kills it. Where is this most expressed? The neurons of the brain. Now you have body killing the brain cells and it's an ongoing inflammation. It doesn't stop, it continues through the life of that individual.’”(98) Included in Hep A (Vaqta), Varicella (Varivax), Dtap+IPV+Hib (Pentacel), Hep A (Havrix), Hep A+Hep B (Twinrix), MMRV (ProQuad), Zoster (Shingles- Zostavax), MMR (MMR-II)
Mueller Hinton agar- “Mueller-Hinton Agar is a medium very rich in nutrients that was originally recommended for the isolation and development of gonococci and meningococci. It is used primarily for sensitivity testing of microorganisms. Approximate formula g/l:
Beef Infusion | 3.0 | Casein Peptone H | 17.5 |
Starch | 1.5 | Agar | 17.0 |
Final pH 7.4 + 0.2 (99) Included in Meningococcal (MCV4-Menactra) and Meningococcal (MPSV4-Menomune)
Neomycin- “Neomycin is an aminoglycoside antibiotic. It kills sensitive bacteria by stopping the production of essential proteins needed by the bacteria to survive. Neomycin may cause permanent hearing loss, nerve damage, and severe kidney damage. Hearing loss can occur even after the drug is stopped. If you already have kidney problems or hearing difficulty, tell your doctor. Notify your doctor immediately if any of the following occur: ringing in your ears, hearing loss, unusual tingling, muscle twitching, seizures. Neomycin may be stopped if you develop kidney or hearing problems. Your doctor will monitor your progress to minimize the possibility of these effects occurring and may run certain tests (eg, hearing and/or kidney tests). Do not use neomycin with other medicines that can cause nerve, kidney, or hearing problems. Other factors that increase the risk of these side effects occurring include advanced age or dehydration (unusual thirst). Neomycin may also cause severe muscle relaxation progressing to paralysis and breathing problems. This possibility increases if you are also taking anesthetics, neuromuscular-blocking agents (eg, succinylcholine), or if you are receiving massive transfusions of citrate anticoagulated blood. Use with other aminoglycosides (eg, paromomycin) or other nephrotoxic/neurotoxic medicines (eg, bacitracin), advanced age, and dehydration all increase the risk of side effects. Potent diuretics (eg, ethacrynic acid, furosemide) should also be avoided because they can cause hearing loss.” (100) Included in Hep A (Vaqta), Influenza (Fluvirin), MMR (MMR-II), Polio (IPV-Ipol), Varicella (Varivax), Dtap+IPV+Hib (Pentacel), MMRV (ProQuad), Zoster (Shingles-Zostavax)
Neomycin sulfate- “Neomycin sulfate is poorly absorbed from the normal gastrointestinal tract. The small absorbed fraction is rapidly distributed in the tissues and is excreted by the kidney in keeping with the degree of kidney function. The unabsorbed portion of the drug (approximately 97%) is eliminated unchanged in the feces. Growth of most intestinal bacteria is rapidly suppressed following oral administration of neomycin sulfate, with the suppression persisting for 48-72 hours. Nonpathogenic yeasts and occasionally resistant strains of Enterobacter aerogenes (formerly Aerobacter aerogenes) replace the intestinal bacteria. As with other aminoglycosides, the amount of systemically absorbed neomycin transferred to the tissues increases cumulatively with each repeated dose administered until a steady state is achieved. The kidney functions as the primary excretory path as well as the tissue binding site, with the highest concentration found in the renal cortex. With repeated dosings, progressive accumulation also occurs in the inner ear. Release of tissue-bound neomycin occurs slowly over a period of several weeks after dosing has been discontinued. Protein binding studies have shown that the degree of aminoglycoside protein binding is low and, depending upon the methods used for testing, this may be between 0% and 30%. NEUROTOXICITY (INCLUDING OTOTOXICITY) AND NEPHROTOXICITY FOLLOWING THE ORAL USE OF NEOMYCIN SULFATE HAVE BEEN REPORTED, EVEN WHEN USED IN RECOMMENDED DOSES. THE POTENTIAL FOR NEPHROTOXICITY, PERMANENT BILATERAL AUDITORY OTOTOXICITY AND SOMETIMES VESTIBULAR TOXICITY IS PRESENT IN PATIENTS WITH NORMAL RENAL FUNCTION WHEN TREATED WITH HIGHER DOSES OF NEOMYCIN AND/OR FOR LONGER PERIODS THAN RECOMMENDED. Serial, vestibular and audiometric tests, as well as tests of renal function, should be performed (especially in highrisk patients). THE RISK OF NEPHROTOXICITY AND OTOTOXICITY IS GREATER IN PATIENTS WITH IMPAIRED RENAL FUNCTION. Ototoxicity is often delayed in onset and patients developing cochlear damage will not have symptoms during therapy to warn them of developing eighth nerve destruction and total or partial deafness may occur long after neomycin has been discontinued.
Neuromuscular blockage and respiratory paralysis have been reported following the oral use of neomycin. The possibility of the occurrence of neuromuscular blockage and respiratory paralysis should be considered if neomycin is administered, especially to patients receiving anesthetics, neuromuscular blocking agents such as tubocurarine, succinylcholine, decamethonium, or in patients receiving massive transfusions of citrate anticoagulated blood. If blockage occurs, calcium salts may reverse these phenomena but mechanical respiratory assistance may be necessary.
Concurrent and/or sequential systemic, oral or topical use of other aminoglycosides, including paromomycin and other potentially nephrotoxic and/or neurotoxic drugs such as bacitracin, cisplatin, vancomycin, amphotericin B, polymyxin B, colistin and viomycin, should be avoided because the toxicity may be additive.” (101) Included in Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix), Hep A (Havrix), Hep A+Hep B (Twinrix)
Nicotinamide adenine dinucleotide- “NADH stands for "nicotinamide adenine dinucleotide (NAD) + hydrogen (H)." This chemical occurs naturally in the body and plays a role in the chemical process that generates energy. People use NADH supplements as medicine. NADH is used for improving mental clarity, alertness, concentration, and memory; as well as for treating Alzheimer’s disease. Because of its role in energy production, NADH is also used for improving athletic endurance and treating chronic fatigue syndrome (CFS). Some people use NADH for treating high blood pressure, high cholesterol, jet lag, depression, and Parkinson’s disease; boosting the immune system; opposing alcohol’s effects on the liver and the hormone testosterone; reducing signs of aging; and protecting against the side effects of an AIDS drug called zidovudine (AZT). Healthcare providers sometimes give NADH by intramuscular (IM) or intravenous (IV) injection for Parkinson's disease and depression. NADH produced by our bodies is involved in making energy in the body. While there is some evidence that suggests NADH supplements might reduce blood pressure, lower cholesterol, help chronic fatigue syndrome by providing energy, and increase nerve signals for people with Parkinson's disease, there isn't enough information to know for sure how or if these supplements work. NADH seems safe for most people when used appropriately and short-term, up to 12 weeks. Most people do not experience any side effects when taking the recommended amount each day, which is 10 mg.” (102) Included in Hib+Hep B (Comvax)
Nonylphenol ethoxylate- “Nonylphenol ethoxylates (NPEs) are surfactants that have been in commerce for over 50 years. Products containing NPEs are used in many sectors, including textile processing, pulp and paper processing, paints, resins and protective coatings, oil and gas recovery, steel manufacturing, pest control products and power generation. A variety of cleaning products, degreasers and detergents are also available for institutional and domestic use. These products have numerous applications, including controlling deposits on machinery, cleaning equipment, and scouring fibres; as wetting and de-wetting agents; in dyeing and machine felt cleaning and conditioning; and in product finishing. NPEs have also been used in a wide range of consumer products, including cosmetics, cleaners, and paints. Nonylphenol ethoxylates are thought to interfere with hormones in animals and may therefore interfere with the development and reproductive system in animals. They are listed as endocrine disrupting chemicals on the EU List (#PANNA). NPE is very toxic to fish and other water-dwelling organisms and is considered a hormone disrupting substance, mimicking estrogen. It degrades relatively readily in the environment to form the even more harmful nonylphenol (NP). Nonylphenol is not readily biodegradable and take months or even longer to degrade in surface waters or in soils and sediments (where it tends to be immobilized). Non-biological degradation is negligible. Bioconcentration and bioaccumulation is significant in water-dwelling organisms and birds, where it has been found in internal organs at between 10 and 1000 times greater than the surrounding environment. Nonylphenols are not broken down effectively in sewage treatment plants.” (103) Included in Influenza (Fluvirin)
Octylphenol ethoxylate (Triton X-100)- “Octylphenol ethoxylates (OPEs) are a group of related chemicals. They are chemically very similar to Nonylphenol ethoxylates (NPEs). Under normal conditions, OPEs are thick liquids or waxy solids, varying in colour from clear to light orange. OPEs are stable. The degree to which they are soluble in water varies, but most are readily soluble in organic (carbon-containing) solvents. OPEs are widely used in cleaning agents. They are also added to paints, coatings, treatments for textiles and chemicals used in paper manufacture. OPEs also have some medical applications. For example, they are added to some drugs to improve the rate at which they are absorbed in the intestine. OPEs are known to be very toxic to wildlife, particularly aquatic organisms. There is also concern that they mimic the behaviour of animal hormones, that they are an "endocrine disruptor". OPEs break down relatively easily into Octyl Phenols (OPs), which are more harmful and can be very persistent in the environment. This persistence means that they can be transported far from the point of original release of OPEs. OPs are accumulated and concentrated by aquatic organisms and birds. It is therefore possible that the presence of OPEs and hence OPs in the environment poses a long-term threat to wildlife on both a local and global scale. Octylphenol ethoxylates can enter the body either by inhalation of air containing octylphenol ethoxylates, ingestion of contaminated food or water, or by dermal contact with octylphenol ethoxylates or products containing octylphenol ethoxylates. There is little evidence available for the full effects of exposure to octylphenol ethoxylates on human health. However, exposure to high levels of octylphenol ethoxylates may cause irritation of the lungs, digestive system, skin and eyes. Octylphenol ethoxylates are thought to interfere with hormones in animals and may therefore interfere with the development and reproductive system in animals. Octylphenol ethoxylates readily degrade in the environment to the more toxic, octylphenol. The International Agency for Research on Cancer has not designated octylphenol ethoxylates in terms of their carcinogenicity. However, exposure to octylphenol ethoxylates at normal background levels is unlikely to have any adverse effect on human health.” (104) Included in Influenza (Fluzone: standard, high-dose)
Ovalbumin- “Ovalbumin is a glycoprotein that comprises 54% of the total proteins of egg white.
Ovalbumin and albumin were some of the very first proteins to be studied. Ovalbumin was first crystallized in 1890 by Hofmeister. In 1938, Neuberger reported that the carbohydrate moiety contained two moles of hexosamine, four moles of mannose, and some unidentified nitrogeneous material.” (105) Included in Influenza (Flulaval)
Phenol- “Exposure to phenol may occur from the use of some medicinal products (including throat lozenges and ointments). Phenol is highly irritating to the skin, eyes, and mucous membranes in humans after acute (short-term) inhalation or dermal exposures. Phenol is considered to be quite toxic to humans via oral exposure. Anorexia, progressive weight loss, diarrhea, vertigo, salivation, a dark coloration of the urine, and blood and liver effects have been reported in chronically (long-term) exposed humans. Animal studies have reported reduced fetal body weights, growth retardation, and abnormal development in the offspring of animals exposed to phenol by the oral route. EPA has classified phenol as a Group D, not classifiable as to human carcinogenicity. The primary use of phenol is in the production of phenolic resins, which are used in the plywood, construction, automotive, and appliance industries. Phenol is also used in the production of caprolactam and bisphenol A, which are intermediates in the manufacture of nylon and epoxy resins, respectively. Other uses of phenol include as a slimicide, as a disinfectant, and in medicinal products such as ear and nose drops, throat lozenges, and mouthwashes.” (106) Included in Hib (PedvaxHIB), Hib+Hep B (Comvax)
Phosphate- “In the body, almost all phosphorus is combined with oxygen, forming phosphate. Bone contains about 85% of the body's phosphate. The rest is located primarily inside cells, where it is involved in energy production. Phosphate is necessary for the formation of bone and teeth. Phosphate is also used as a building block for several important substances, including those used by the cell for energy, cell membranes, and DNA (deoxyribonucleic acid). The body obtains phosphate from foods and excretes it in urine and stool.” (107) Included in Varicella (Varivax)
Phosphate buffers- “Gomori buffers, the most commonly used phosphate buffers, consist of a mixture of monobasic dihydrogen phosphate and dibasic monohydrogen phosphate. By varying the amount of each salt, a range of buffers can be prepared that buffer well between pH 5.8 and pH 8.0. Phosphates have a very high buffering capacity and are highly soluble in water. However, they have a number of potential disadvantages: Phosphates inhibit many enzymatic reactions and procedures that are the foundation of molecular cloning, including cleavage of DNA by many restriction enzymes, ligation of DNA, and bacterial transformation. Because phosphates precipitate in ethanol, it is not possible to precipitate DNA and RNA from buffers that contain significant quantities of phosphate ions.” (108) Included in Hep B (Engerix-B), Meninagococcal (MCV4-Menactra), Hep A+Hep B (Twinrix), Influenza (Fluzone)
Polymyxin (polymyxin B) (polymyxin B sulfate)- “Polymyxin B (polymyxin b sulfate) sulfate is a drug of choice in the treatment of infections of the urinary tract, meninges, and bloodstream caused by susceptible strains of Ps. aeruginosa. It may also be used topically and subconjunctivally in the treatment of infections of the eye caused by susceptible strains of Ps. aeruginosa. Nephrotoxic reactions: Albuminuria, cylindruria, azotemia, and rising blood levels without any increase in dosage. Neurotoxic reactions: Facial flushing, dizziness progressing to ataxia, drowsiness, peripheral paresthesias (circumoral and stocking glove), apnea due to concurrent use of curariform muscle relaxants, other neurotoxic drugs or inadvertent overdosage, and signs of meningeal irritation with intrathecal administration, e.g., fever, headache, stiff neck and increased cell count and protein cerebrospinal fluid. Other reactions occasionally reported: Drug fever, urticarial rash, pain (severe) at intramuscular injection sites, and thrombophlebitis at intravenous injection sites.” (109) Included in Influenza (Fluvirin), Polio (IPV-Ipol), Dtap+IPV (Kinrix), Dtap+Hep B+IPV (Pediarix), Dtap+IPV+Hib (Pentacel)
Porcine circovrius- “Circoviruses are an unusual and ubiquitous class of animal viruses characterized by circular single-stranded DNA genomes. The circoviruses are non-enveloped, icosahedral viruses and have the smallest genomes of all known animal viruses ranging between 1.7-2.3 kilobases. Circovirus are present in many animals including avian, porcine, bovine, murine, and human hosts2. Although there are no known human pathologies associated with circovirus, outbreaks of avian and porcine circovirus impart recurring economic loss to livestock industries and continue to be a recurring problem worldwide. The avian circovirus, chicken anemia virus (CAV), infects young chickens and induces massive apoptosis in erythroblasts resulting a characteristic anemia and immunosuppression. Disease causing circovirus infections are widespread among avian hosts and have been documented in many species including geese, pigeon, gulls, finches and ostrich3. Circoviruses are commonly cause pathologies in wild birds as well and are regarded as an important emerging pathogen with potentially serious effects for domesticated and natural avian fauna.” (110) Included in Rotavirus (RotaTeq), Rotavirus (Rotarix)
Potassium aluminum sulfate (potash alum)- “Used in dyeing and printing fabrics; manufacturing dyes, lakes, paper, vegetable glue, marble cement, porcelain cement, explosives, aluminum salts, artificial stones, and statuary; tanning; waterproofing; hardening gelatin; purifying water; clarifying sugar; hardening plaster casts; and electrolytic copper plating; Also used as a catalyst in synthesis of ammonia, a mordant in staining (with carmine, eosin, and hematoxylin), a clarifier (as alumina cream), a hardening agent in microscopy, an additive (matches, paints, baking powder, and foods), a water correcting agent used in brewing industry, an astringent, a veterinary antiseptic and antimycotic, and in taxidermy; [HSDB] Used as a coagulating agent for latex and as a styptic pencil; [CHEMINFO] Potassium aluminum sulfate (alum) is used as a hardener in photographic processing; Also used as a mordant in textile dyeing (textile arts). Patients who had died with dialysis encephalopathy syndrome had brain gray matter aluminum levels that were 3 times higher (approximately 12 mg/kg dry weight) than those seen in patients who had been comparably dialyzed but did not have dialysis encephalopathy syndrome (approximately 4 mg/kg dry weight). Both of these groups were markedly higher than the 1 mg/kg dry weight level seen in controls. These data clearly indicate elevated brain levels of aluminum in dialyzed patients and emphasize the fact that only the highest levels of brain aluminum are associated with dialysis encephalopathy syndrome.” (111) “Aluminum has been long known to be neurotoxic, with mounting evidence that chronic exposure is a factor in many neurological diseases, including dementia, autism, and Parkinson's disease. However, definitive scientific proof is difficult to establish due toth the lack of longitudinal studies, as well as pushback from industries that use aluminum in their products. Despite the shortage of conclusive studies, mounting scientific evidence really leaves little room for doubt.
Case in point: a new case study from Keele University in the UK1 unequivocally shows high levels of aluminum in the brain of an individual exposed to aluminum at work, who later died from Alzheimer's disease. While aluminum exposure has been implicated in Alzheimer's and a number of other neurological diseases, this case claims to be "the first direct link" between Alzheimer's disease and elevated brain aluminum following occupational exposure. Vaccines present a particularly problematic source of toxic metal exposure. Aluminum is the most commonly used vaccine adjuvant and is considered "safe" even though research shows it may induce serious immunological disorders and neurological complications in humans. In the video above, Dr. David Ayoub discusses how the aluminum in vaccines may be even more dangerous than mercury. The number of aluminum-containing vaccines children receive today has quadrupled over the past 30 years. In the 1970s, children got only four aluminum-containing vaccines in their first 18 months of life, but now they typically receive 17. And as children's aluminum burden has increased, so has the prevalence of childhood neurological disorders. In one school, 90 percent of the children developed ADHD during the course of a single school year, and their toxicity profiles all revealed massive amounts of aluminum. Aluminum is also in vaccines and is used as an adjuvant. If you go by the aluminum content on vaccine labels, the amount kids are getting is excessive, but if you add in the aluminum NOT listed on the labels—"accidental exposure" due to contamination—it's a much more serious problem. Dr. Ayoub cites one study that found five to six times more aluminum in vaccines than what was actually listed on the labels. When you review the signs and symptoms of aluminum toxicity, they are shockingly similar to the symptoms of autism, ADHD, Alzheimer's, Parkinson's, and other neurological diseases. Vaccine adjuvants can cause serious chronic brain inflammation. Aluminum targets your cerebellum and autonomic nervous system—the part responsible for biological processes over which you have no conscious control (breathing, blood pressure, balance, coordination, etc.). When you look at the MSDS sheet for aluminum, you will see symptoms strikingly similar to those in common neurological diseases, including memory problems, speech impairments and aphasia, dementia, depression, muscle weakness, motor disturbances, and other neurological difficulties. The list goes on and on.” (112) Included in Hep B (Recombivax), Hib+Hep B (Comvax)
Potassium chloride- “A white crystal or crystalline powder used in buffers; fertilizers; and explosives. It can be used to replenish electrolytes and restore water-electrolyte balance in treating hypokalemia. Inhalation can cause cough or sore throat. Ingestion can cause diarrhoea, nausea, vomiting, weakness, convulsions. The substance is irritating to the eyes and respiratory tract. Ingestion of large amounts could cause effects on the cardiovascular system. This may result in cardiac dysrhythmia.” (113) Included in MMRV (ProQuad)
Potassium phosphate monobasic- “Potassium Phosphate, Monobasic is a reagent with a very high buffering capacity and is widely used in molecular biology, biochemistry, and chromatography. Potassium phosphate occurs in several forms: monobasic (KH2PO4), dibasic (KH2PO4), and tribasic (K3PO4). Neutral potassium phosphate buffer solutions may be prepared with a mixture of the monobasic and dibasic forms to varying degrees, depending on the desired pH. Potassium Phosphate buffers are very useful in numerous applications, but with the following limitations: precipitation of Ca2+ and Mg2+, inhibition of restriction enzyme activity, and interference in DNA ligation or bacterial transformation protocols. Has been used to study the effects of freezing and thawing on the stability of proteins sensitive to conformational changes; it was found that KP buffers offered improved pH stability as opposed to NaP buffers. Potassium Phosphate has also been used for the extraction of keratohyalin protein from bovine tissue. It is an excellent source of phosphorus and potassium, has been used as a fungicide, and in its crystalline state it is noted for its nonlinear optical properties.” (114) “This medication helps control the amount of calcium in the body and urine. It works by making the urine more acidic. It is used to prevent calcium kidney stones. It is also used to decrease the amount of ammonia in urine, thereby reducing odor and skin irritation caused by high-ammonia urine. This medication is also given to help certain antibiotics for bladder infections (e.g., methenamine) work better. Nausea, vomiting, diarrhea, dizziness, or headache may occur. May also cause bone/joint aches, muscle cramps, stomach pain, confusion, fast/irregular heartbeat, unusual weakness, tingling/numbness of the hands/feet, and change in the amount of urine.” (115) Included in Influenza (Flumist), Varicella (Varivax)
Polysorbate 80 (Tween 80)- “Polyoxyethylene-sorbitan-20-monooleate (also known as polysorbate 80 and Tween 80) is a solubilizing agent ubiquitously used in nutritives, creams, ointments, lotions, and multiple medical preparations (e.g., vitamin oils, vaccines, and anticancer agents) and as an additive in tablets. Whereas its relevance as a contact allergen has declined during the past decades, it is of current relevance as a "hidden" inductor of anaphylactoid reactions. Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.” (116) “Side effects include abdominal or stomach pain, accumulation of pus, arm, back, or jaw pain, blurred vision, breathing problems (irregular, noisy, or trouble when resting), chest pain, discomfort, tightness, or heaviness, chills, confusion, cough producing mucus, decrease in the amount of urine, diarrhea, dilated neck veins, dizziness, fainting, or lightheadedness, dry mouth, fast, slow, or irregular heartbeat, fatigue or tiredness (extreme or unusual), fever, headache, nausea, pain, tenderness, swelling, or warmth over injection site, pounding in the ears, rapid breathing, rapid or pounding pulse, shortness of breath, skin discoloration at the injection site, sunken eyes, sweating, swelling of the ankles, face, fingers, feet, hands, or lower legs, thirst, trouble with breathing, unconsciousness, vomiting, weight gain, wheezing, wrinkled skin, anxiety, convulsions, difficulty with speaking (slow speech or unable to speak), double vision, trouble with thinking, trouble with walking, unable to move the arms, legs, or face muscles (including numbness and tingling), fever and sore throat, hives, itching, pale skin, skin rash, unusual tiredness or weakness, constipation, general feeling of discomfort or illness, lack or loss of strength, loss of appetite, muscle aches, pains, or stiffness, pain in the joints, runny nose, shivering, sneezing, trouble with sleeping. Clinical studies have shown darbepoetin alfa (albumin) to increase the risk of serious side effects (eg, blood clots, stroke, heart attack, heart failure) and death in some cases. It has also been shown to increase the risk of tumor growth in patients with advanced cancer.” (117)Included in Hep A (Havrix), Hep A+Hep B( Twinrix), Dtap+IPV+Hib (Pentacel), Dtap (Infanrix), HPV (Gardasil), Influenza (Flulaval), Pneumococcal (PCV13- Prevnar), Rotavirus (RotaTeq), Tdap (Boostrix), Dtap+IPV (Kinrix), Dtap+Hep B+ IPV (Pediarix)
Recombinant human albumin- “Genetically engineered human albumin derived from yeast. Currently, only the MMR vaccine contains genetically engineered human protein, which is produced under the brand name recombumin and referred to as "recombinant human albumin" in the package insert.” (118) “Albumin (human) is used for treating a variety of conditions, including shock due to blood loss in the body, burns, low protein levels due to surgery or liver failure, and as an additional medicine in bypass surgery. Albumin (human) is a concentrate of plasma proteins from human blood. It works by increasing plasma volume or serum albumin levels. Side effects include anaphylactoid reactions, fever, chills, rash, nausea, vomiting, tachycardia, hypotension. Dermatologic side effects have included urticaria, skin rash, pruritus, edema, and erythema. Nervous system side effects have included headache, chills, and febrile reactions. Cardiovascular side effects have included hypotension. Gastrointestinal side effects have included nausea, vomiting and increased salivation. Respiratory side effects have included bronchospasm.” (119) Included in MMR (MMR-II)
Semi- synthetic medium- “Only three vitamins (pantothenate, p-amino benzoic acid, nicotinic acid) and two amino acids (serine, glutamine) were required in the growth medium for Gluconobacter oxydans which allowed the concentration of yeast extract to be reduced to 5–10% of the previous concentration. When compared with data from cultivations with complex media, the new medium gave a lower yield (about 0.02 g biomass per g glycerol) and comparable growth rate (0.24 to 0.38 h−1) but a higher productivity (10.3 g dihydroxyacetone/gh).” (120) “A semisynthetic medium, containing yeast extract as the only non defined component and glucose, glycerol, Tween 80 and mineral salts, has been developed to grow the strains of Propionibacterium acnes Beck 2037, Gerrath 2038 and Vogel 2039, at a rate comparable to that of complex media. An average of 10(12) cells per 1 (equivalent to approximately 1.5 g/l dry weight) was usually achieved. These yields are appropriated for biochemical and immunological studies, e.g. cell wall preparation, polysaccharides isolation, etc. In this work, some properties of the cell walls (sugar and amino acid composition) and the antigenic polysaccharides (neutral and amino sugar components) are described.” (121) Included in Hib (Hiberix)
Sodium bicarbonate (baking soda)- “Treating metabolic acidosis (a condition in which there is too much acid in the body) and certain drug intoxications, and replacing bicarbonate lost due to severe diarrhea. It may also be used for other conditions as determined by your doctor. Sodium bicarbonate is an electrolyte. It works by neutralizing excess acid in the blood. It may also replace bicarbonate when there are excess losses from the body. Side effects include frequent urge to urinate, headache (continuing), loss of appetite (continuing), mood or mental changes, muscle pain or twitching, nausea or vomiting, nervousness or restlessness, slow breathing, swelling of feet or lower legs, unpleasant taste, unusual tiredness or weakness. The respiratory drive may be suppressed after bicarbonate administration due to increased venous C02 concentration. Without adequate ventilation, worsened systemic acidosis could develop. Respiratory side effects have included suppressed respiratory drive. Rapid infusion of hyperosmolar sodium bicarbonate has been associated with intraventricular hemorrhage in the pediatric literature. Irritability and tetany have been associated with sodium bicarbonate-induced alkalosis or hypernatremia. Due to greater permeability of the blood-brain barrier to hydrogen than to bicarbonate, the pH of cerebrospinal fluid may significantly decrease during sodium bicarbonate administration, which can cause mental stupor or coma. Nervous system side effects have included irritability, tetany, mental stupor, coma, and intraventricular hemorrhage. Local side effects have included IV site pain, venous irritation, and extravasation. Cellulitis, tissue necrosis, ulceration, or skin sloughing have possibly been the result of extravasation. A slow rate of administration of a properly diluted solution into a large bore needle and vein is recommended if IV administration is necessary. Cardiovascular side effects have included decreased cardiac contractility possibly resulting from infusion of sodium bicarbonate in patients with severe acidosis. Experimentally, the administration of intravenous hypertonic sodium bicarbonate has been associated with increased serum osmolality, decreased ionized serum calcium (which is associated with decreased myocardial contractility), and peripheral vasodilation. Some experts recommend invasive hemodynamic monitoring in acidotic patients before the administration of bicarbonate. Gastrointestinal side effects associated with oral administration have rarely included gastric rupture. As an antacid, sodium bicarbonate, especially after excess food or liquid, can cause excess gas release (when combined with gastric acid). The mortality associated with gastric rupture is as high as 65%. Urinary alkalinization from bicarbonate can cause a falsely positive colorimetric assay for protein. Renal side effects have rarely included "False proteinuria".” (122) Included in MMRV (ProQuad)
Sodium borate (borax)- “Borax (also known as sodium borate decahydrate; sodium pyro borate; borax; sodium tetraborate decahydrate; sodium biborate) is a natural mineral compound (Na2B4O7 • 10H2O). It was discovered over 4000 years ago. Borax is usually found deep within the ground, although it has been mined near the surface in Death Valley, California since the 1800s. Although it has numerous industrial uses, in the home borax is used as a natural laundry booster, multipurpose cleaner, fungicide, preservative, insecticide, herbicide, disinfectant, desiccant, and ingredient in making 'slime'. Borax crystals are odorless, whitish (can have various color impurities), and alkaline. Borax is not flammable and is not reactive. It can be mixed with most other cleaning agents, including chlorine bleach. Borax may also be used as an insecticide to kill roaches, ants, and fleas. In fact, it is also toxic to people. Signs of chronic toxic exposure include red and peeling skin, seizures, and kidney failure. The estimated lethal dose (ingested) for adults is 15-20 grams; less than 5 grams can kill a child or pet. For this reason, borax should not be used around food. More commonly, borax is associated with skin, eye, or respiratory irritation. It is also important to point out that exposure to borax may impair fertility or cause damage to an unborn child.” (123) “Borax had effects on immune cell proliferation (lymphocyte proliferation) and induced sister chromatid exchange in human chromosomes. Toxicity of borax may lead to cellular toxicity and genetic defect in human.” (124) “Effects from/ ingestion /include/ abdominal pain, diarrhea, headache, nausea, vomiting, weakness, convulsions.” This website includes a lot of peer reviewed reports on the effects of borax on the human body. (125) Included in Hep A (Vaqta), HPV (Gardasil), Hib+Hep B (Comvax)
Sodium Citrate (citric acid)- “Sodium citrate/citric acid is used to make urine less acidic and therefore prevent formation of kidney stones. Sodium citrate/citric acid also is useful as a buffer and neutralizing agent for gastric acid. Sodium citrate is broken down to sodium bicarbonate which decreases the acidity of urine, increasing the excretion of substances that cause kidney stones. Common side effects of sodium citrate/citric acid are nausea, vomiting, diarrhea, stomach pain, and water retention. It should not be used in patients with kidney failure. It is not known whether sodium citrate/citric acid enters breast milk; therefore, it is best to be cautious before using it in nursing mothers.” (126) “You should not use this medication if you have kidney failure, severe heart damage (such as from a prior heart attack), Addison's disease (an adrenal gland disorder), high levels of potassium in your blood (hyperkalemia), or if you are severely dehydrated or have heat cramps. Avoid using antacids without your doctor's advice, including household baking soda (sodium bicarbonate). Antacids that contain aluminum or sodium can interact with citric acid and sodium citrate, causing a serious electrolyte imbalance or aluminum toxicity. Serious side effects of citric acid and sodium citrate include muscle twitching or cramps, swelling or weight gain, weakness, mood changes, rapid and shallow breathing, fast heart rate, restless feeling, black or bloody stools, severe diarrhea, or seizure (convulsions).” (127) Included in Rotavirus (RotaTeq)
Sodium deoxycholate- ” “Detergents area class of molecules whose unique properties enable disruption or formation of hydrophobic and hydrophilic interactions among molecules in biological samples. Sodium Deoxycholate is a water-soluble ionic detergent commonly used for membrane prote in and lipid isolation, cell lysis, and liposome preparation. This detergent also
is used to supplement cell culture media and to prevent nonspecific binding in affinity chromatography. Sodium Deoxycholate is used to regenerate immobilized polymyxin B (Detoxi-Gel D™ Endotoxin Removing Gel, Product No. 20339). Immobilized polymyxin B is an effective tool for removing endotoxins (lipopolysaccharide or LPS) from biological samples.
Sodium Deoxycholate is the most effective reagent for removing LPS from immobilized polymyxin B, allowing reuse of this ligand for additional endotoxin removal.” (128) “Bile acids are often refluxed into the lower oesophagus and are candidate carcinogens in the development of oesophageal adenocarcinoma. We show here that the secondary bile acid, deoxycholic acid (DCA), is the only one of the commonly refluxed bile acids tested here, to show genotoxicity, in terms of chromosome damage and mutation induction in the human p53 gene. This genotoxicity was apparent at both neutral and acidic pH, whilst there was a considerable increase in bile-induced toxicity at acidic pH. The higher levels of cell death and low cell survival rates at acidic pH may imply that acid bile exposure is toxic rather than carcinogenic, as dead cells do not seed cancer development. We also show that DCA (at neutral and acid pH) induced the release of reactive oxygen species (ROS) within the cytoplasm of exposed cells. We further demonstrate that the genotoxicity of DCA is ROS mediated, as micronucleus induction was significantly reduced when cells were treated with DCA + the antioxidant vitamin C. In conclusion, we show that DCA, is an effective genotoxin at both neutral and acidic pH. As bile acids like DCA can induce DNA damage at neutral pH, suppressing the acidity of the refluxate will not completely remove its carcinogenic potential. The genotoxicity of DCA is however, ROS dependent, hence antioxidant supplementation, in addition to acid suppression may block DCA driven carcinogenesis in Barrett's patients.” (129) “Disruption of the blood-brain barrier (BBB) is a characteristic finding in common neurological disorders. Human data suggest BBB disruption may underlie cerebral dysfunction. Animal experiments show the development of epileptiform activity following BBB breakdown. In the present study we investigated the neurophysiological, structural and functional consequences of BBB disruption. Adult rats underwent focal BBB disruption in the rat sensory-motor cortex using the bile salt sodium deoxycholate (DOC). Magnetic resonance imaging in-vivo showed an early BBB disruption with delayed reduction in cortical volume. This was associated with a reduced number of neurons and an increased number of astrocytes. In-vitro experiments showed that the threshold for spreading depression and the propagation velocity of the evoked epileptic potentials were increased 1 month after treatment. Furthermore, animals' motor functions deteriorated during the first few weeks following BBB disruption. Treatment with serum albumin resulted in a similar cell loss confirming that the effect of DOC was due to opening of the BBB. Our findings suggest that delayed neurodegeneration and functional impairment occur following the development of the epileptic focus in the BBB-permeable cerebral cortex” (130) Included in Influenza (Flulaval)
Sodium dihydrogen phosphate dihydrate- “Sodium phosphate monobasic dihydrate is a reagent with very high buffering capacity widely used in molecular biology, biochemistry and chromatography. Sodium phosphate dibasic is highly hygroscopic and water soluble. Useful in conjunction with Sodium Phosphate, Dibasic in the preparation of biological buffers. Used in many applications including the purification of antibodies.” (131) Has a number of side effects consisting , lethargy, hyperpyrexia, diarrhea, carpal spasms, coma, renal acute failure, mucosal lesions, aphthous lesions. This website has a lot of peer reviewed reports of side effects. (132)Included in HPV (Cervarix)
Sodium hydroxide (lye or caustic soda)- “Sodium hydroxide is a very strong chemical that is also known as lye and caustic soda. This article discusses poisoning from touching, breathing in (inhaling), or swallowing sodium hydroxide. Sodium hydroxide is found in many industrial solvents and cleaners, including flooring stripping products, brick cleaners, cements, and many others. It may also be found in certain household products, including aquarium products, clinitest tablets, drain cleaners, hair straighteners, metal polishes, and oven cleaners. Side effects include Breathing difficulty (from inhalation), lung inflammation, sneezing, throat swelling (which may also cause breathing difficulty), blood in the stool, burns of the esophagus (food pipe) and stomach, diarrhea, severe abdominal pain, vomiting, possibly bloody, drooling, severe pain in the throat, severe pain or burning in the nose, eyes, ears, lips, or tongue, vision loss, collapse, low blood pressure (develops rapidly), severe change in pH (too much or too little acid in the blood), and shock.” (133) Included in Rotavirus (RotaTeq)
Sodium phosphate (dibasic and monobasic)- “Sodium phosphate dibasic and sodium phosphate monobasic combination is used to clean or empty your bowels before an imaging procedure called colonoscopy. This medicine works by cleaning your colon and causing you to have diarrhea. Side effects include allergic reaction: itching or hives, swelling in your face or hands, swelling or tingling in your mouth or throat, chest tightness, trouble breathing, blood in your urine, lower back pain, side pain, or sharp back pain just below your ribs, confusion, weakness, and muscle twitching, decrease in how much or how often you urinate, dizziness or fainting,
dry mouth, increased thirst, muscle cramps, nausea or vomiting, fast, pounding, or uneven heartbeat, red or black stools, seizures, severe stomach pain, nausea, vomiting, or bloating.” (134) Included in MMRV (ProQuad), Zoster (Shingles- Zostavax), Varicella (Varivax)
Sorbitol- “A polyhydric alcohol with about half the sweetness of sucrose. Sorbitol occurs naturally and is also produced synthetically from glucose. It was formerly used as a diuretic and may still be used as a laxative and in irrigating solutions for some surgical procedures. It is also used in many manufacturing processes, as a pharmaceutical aid, and in several research applications. Ingestion hazard: abdominal cramps, abdominal pain, diarrhoea. May cause respiratory tract irritation. May cause skin irritation. May cause eye irritation. The substance may cause effects on the gastrointestinal tract. Finely dispersed particles form explosive mixtures in air.” (135) Included in MMR (MMR-II), MMRV (ProQuad), Rotavirus (Rotarix)
Soy Peptone- “This peptone is obtained by papaic digestion of soya flour. In addition to its nitrogen constituents, this peptone has a high carbohydrate content and is suitable for many purposes. It is widely used in culture media and is often used for the cultivation of many fastidious organisms and where rapid, luxuriant growth is required. However, due to this high content of sugar it is not recommendable for fermentation assays.” (136) “Soybeans contain phytoestrogens, which mimic the body’s natural estrogen hormones. For men, this can lead to a testosterone imbalance, infertility, low sperm count, and increased risk of cancers. For women, it can cause estrogen dominance, which has been linked to infertility, menstrual troubles and cancer. These phytoestrogens are so strong that a baby consuming only soy formula is consuming the equivalent hormones of 4 birth control pills a day. The high levels of phytic acid in soy inhibit the body’s ability to absorb important minerals, including zinc, calcium, copper, iron and magnesium (which many people are dangerously deficient in already). Soy also contains protease inhibitors, which can block the enzymes that are necessary for the digestion of certain proteins. The goitrogens in soy are potent anti-thyroid compounds that can lead to endocrine disruption and thyroid disorders. Infants on soy formula have a much higher risk of autoimmune thyroid disease. (note: cruciferous vegetables like broccoli, cauliflower and cabbage have these properties as well, though they are lessened greatly by cooking. Cooking does not remove these compounds from soy based foods!) Soy is often promoted as an alternative food for celiac and gluten intolerant people, but its lectins can be harmful to the intestines and prevent healing even when gluten is removed.” (137) Included in Hep B (Recombivax), Hib+ Hep B (Comvax)
Streptomycin- “Treating tuberculosis (TB) and infections caused by certain bacteria.
Streptomycin is an aminoglycoside. It works by killing sensitive bacteria by stopping the production of essential proteins needed by the bacteria to survive. Some more common side effects include black, tarry stools, burning, crawling, itching, numbness, prickling, "pins and needles", or tingling feelings, chest pain, chills, clumsiness, cough, dizziness or lightheadedness,
feeling of constant movement of self or surroundings, fever, large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs, nausea, painful or difficult urination,
sensation of spinning, shortness of breath, sore throat, sores, ulcers, or white spots on the lips or in the mouth, swollen glands, unsteadiness, unusual bleeding or bruising, unusual tiredness or weakness, vomiting. Less common side effects include back, leg, or stomach pains, bleeding gums, bloody or cloudy urine, blurred vision, change in vision, dark urine, deafness, difficulty with breathing, difficulty with swallowing, dry mouth, fast heartbeat, general body swelling, headache, hives, impaired vision, itching, loss of appetite, muscle weakness, nosebleeds, pain in lower back or side, pale skin, pinpoint red spots on the skin, puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue, skin rash, thirst, tightness in the chest, wheezing, yellowing of the eyes or skin. Rare side effects include change in the frequency of urination or amount of urine, drowsiness, increased thirst, swelling of the feet or lower legs, and weakness. Severe toxic nerve reactions are possible for patients with kidney problems who use this medication. Kidney function and complete blood counts should be closely monitored by a healthcare provider while taking this medication. Appropriate medical equipment should be available for patients taking this medication.” (138) Included in Polio (IPV-Ipol)
Succinate buffer- “A buffer keeps the pH of a solution constant by taking up protons that are released during reactions, or by releasing protons when they are consumed by reactions. The observation that partially neutralised solutions of weak acids or bases are resistant to changes in pH when small amounts of strong acids or bases are added led to the concept of the ‘buffer’” (139) “Succinate buffer is prepared by dissolving succinic acid in distilled water. The pH of the buffer is adjusted with 0.2N sodium hydroxide.” (140) Included in Pneumococcal (PCV13- Prevnar)
Sucrose (Table sugar)- “Sucrose or table sugar is obtained from sugar cane or sugar beets.
The glucose and fructose units are joined by an acetal oxygen bridge in the alpha-1 on the glucose and beta-2 on the fructose orientation. The structure is easy to recognize because it contains the six member ring of glucose and the five member ring of fructose.” (141) Included in Influenza (Flumist), Influenza (Fluzone), Varicella (Varivax), MMRV (ProQuad), Zoster (Shingles- Zostavax), Rotavirus (Rotarix), Rotavirus (Rotataq)
Thimerosal- “Delayed-type hypersensitivity reactions from thimerosal exposure are well-recognized. Identified acute toxicity from inadvertent high-dose exposure to thimerosal includes neurotoxicity and nephrotoxicity. Limited data on toxicity from low-dose exposures to ethylmercury are available, but toxicity may be similar to that of methylmercury. Chronic, low-dose methylmercury exposure may cause subtle neurologic abnormalities. Depending on the immunization schedule, vaccine formulation, and infant weight, cumulative exposure of infants to mercury from thimerosal during the first 6 months of life may exceed EPA guidelines.” (142) “Dr. Hooker, a PhD scientist, worked with two members of Congress to craft the letter to the CDC that recently resulted in his obtaining long-awaited data from the CDC, the significance of which is historic. According to Hooker, the data on over 400,000 infants born between 1991 and 1997, which was analyzed by CDC epidemiologist Thomas Verstraeten, MD, “proves unequivocally that in 2000, CDC officials were informed internally of the very high risk of autism, non-organic sleep disorder and speech disorder associated with Thimerosal exposure.” (143) “Mercury has no positive role in the human body; in fact a safe level of mercury exposure is very difficult to determine. It can be present in the environment in several different forms, and while all forms of mercury are toxic to humans, the pattern of toxicity varies with its chemical form, the route of exposure, the amount, the duration and timing of exposure, and the vulnerability of the person exposed. For example, pure elemental mercury (also known as quicksilver or Hg) is liquid at room temperature. If ingested, quick-silver has very low toxicity because it is not absorbed by the gastrointestinal tract and is eliminated completely in the stool. If quicksilver is agitated or heated, however, the liquid mercury becomes a vapour which is readily absorbed by inhalation and is highly toxic to the lungs and central nervous system. The nervous system is the primary target of mercury toxicity, but, depending upon the specific exposure, the kidneys, liver and lungs are also important targets. Table 1 (Page 21) gives an overview of the different forms of mercury, their uses, routes of exposure and their toxicity. High doses of mercury can be fatal to humans, but even relatively low doses of mercury containing compounds can have serious adverse impacts on the developing nervous system, and have recently been linked with possible harmful effects on the cardiovascular, immune and reproductive systems. Mercury and its compounds affect the central nervous system, kidneys, and liver and can disturb immune processes; cause tremors, impaired vision and hearing, paralysis, insomnia and emotional instability. During pregnancy, mercury compounds cross the placental barrier and can interfere with the development of the foetus, and cause attention deficit and developmental delays during childhood. Foetuses and young children are actively developing and therefore most at risk from health effects including neurological damage, resulting in behavioural problems and learning disabilities. Neurological effects: Low doses of methyl mercury in pregnant women have been shown to have impacts on the foetus. In a major review of mercury health studies the US National Academy of Sciences stated: ‘Chronic, low-dose prenatal methylmercury exposure from maternal consumption of fish has been associated with ...poor performance on neurobehavioral tests, particularly on tests of attention, fine-motor function, language, visual-spatial abilities (e.g. drawing) and verbal memory.’ Cardiovascular effects: Two recent epidemiological studies found associations between exposure to low levels of methylmercury and adverse cardiovascular effects. The US National Academy of Sciences concludes that additional studies are needed to better characterise the effect of methylmercury exposure on blood pressure and cardiovascular function at various stages of life. The European Commission also notes recent evidence suggesting that mercury from fish and seafood may promote or predispose the development of heart disease.” (144) Included in Influenza (Fluvirin), Influenza (Flulaval), Influenza (Fluzone: High dose), Meningococcal (MPSV4-Menomune)
Watson Scherp media- The only information I could find on this is that meningitis is cultivated in it. Included in Meningococcal (MCV4- Menactra), Meningococcal (MPSV4- Menomune)
WI-38 human diploid lung fibroblasts- “To date, there are two human diploid cell lines which were originally prepared from tissues of aborted foetuses (in 1964 and 1970) and are used for the preparation of vaccines based on live attenuated virus: the first one is the WI-38 line (Winstar Institute 38), with human diploid lung fibroblasts, coming from a female foetus that was aborted because the family felt they had too many children (G. Sven et al., 1969). It was prepared and developed by Leonard Hayflick in 1964 (L. Hayflick, 1965; G. Sven et al., 1969)3 and bears the ATCC number CCL-75. WI-38 has been used for the preparation of the historical vaccine RA 27/3 against rubella (S.A. Plotkin et al, 1965)” (145) Included in MMR (MMR-II), MMRV (ProQuad)
Xanthan- “Xanthan gum is a sugar-like compound made by mixing aged (fermented) sugars with a certain kind of bacteria. It is used to make medicine. Xanthan gum is used for lowering blood sugar and total cholesterol in people with diabetes. It is also used as a laxative. Xanthan gum swells in the intestine, which stimulates the digestive tract to push stool through. It also might slow the absorption of sugar from the digestive tract and work like saliva to lubricate and wet the mouth in people who don't produce enough saliva. Side effects may include nausea, vomiting, appendicitis, hard stools that are difficult to expel (fecal impaction), narrowing or blockage of the intestine, or undiagnosed stomach pain.” (146) Included in Rotavirus (Rotarix)
Yeast and yeast protein- “Expression of proteins in yeast is a common alternative to prokaryotic and higher eukaryotic expression. Yeast cells offer many of the advantages of producing proteins in microbes (growth speed, easy genetic manipulation, low cost media) while offering some of the attributes of higher eukaryotic systems (post translational modifications, secretory expression). Several yeast protein expression systems exist in organisms from the genera Saccharomyces, Pichia, Kluyveromyces, Hansenula and Yarrowia.” (147) “A new study indicates that a significant factor in causing them may be the common bakers or brewers yeast,Saccharomyces cerevisiae used in many vaccinations, including HepB, which is given to nearly all newborn babies in the United States before they’re a day old. The specific part of S. cerevisiae that’s of concern is mannan, which is found in the cell walls of yeasts and also in mammalian glycoproteins. These glycoproteins are found in cell walls, connective tissues like collagen, gastrointestinal mucous secretions, and blood plasma. They perform many functions. Obviously, if the immune system goes on the attack against mannan, it can be devastating. Yet, that appears to be happening in many autoimmune diseases. These diseases happen when the body’s own defense system turns on itself, resulting in life-eroding conditions like rheumatoid arthritis, Crohn’s disease, inflammatory bowel disease, systemic lupus erythematosus, anti-phospholipid syndrome, multiple sclerosis, diabetes mellitus type 1, and even heart disease.
The Centers for Disease Control (CDC) has no doubt about the increase in autoimmune diseases[2] and the National Institutes of Health (NIH) has produced a nice document outlining their approach to dealing with it. The “Autoimmune Diseases Research Plan” discusses their approach to dealing with the issue, including the type of research they’re supporting. Nowhere is there any indication that vaccinations are being considered as a potential cause. Yeast is, of course, used to make bread rise and create the alcohol in beer. So how can it suddenly turn into an enemy? The answer is in how it enters the body, and what enters with it. The purpose of a vaccine is to create a localized storm in the immune system so that it will respond to a co-injected substance, which may be a weakened microbe or a small bit of a microbe, by creating antibodies to it. An irritant, called an adjuvant, is what causes the immune system storm, and the microbe is called an antigen. The catch is that other substances injected with the antigen and adjuvant may also be seen as antigens. If one of those substances is similar to something that naturally exists in the body, then the immune system may create antibodies to part of its own body, creating an autoimmune disease. Parts of the mannan in yeast are similar or identical to parts of the human body. So S. cerevisiae—yeast—used in vaccines has the potential of causing autoimmune disorders. In fact, S. cerevisiaeis used in a variety of ways in vaccines. It is, when used whole, a potent adjuvant. On top of that, genetic manipulation is now being used on it to create artificial antibodies, so S. cerevisiae is becoming more common in vaccines. The researchers who focused on autoimmune aspects of S. cerevisiae (yeast) found significant correlations between yeast’s mannan and known autoimmune antigens in several autoimmune diseases. They found close and, in some instances, exact matches of the genetic sequences. For example, in the case of rheumatoid arthritis, the percent found to match were:
Rheumatoid arthritis
- Rheumatoid factor: 60%
- Bip/GRP78: 71%
- gp130-RAPS: 80%
- EIF4G1: 88%
- Anti-citrullinated collagen type 2: 100%
Not only were there significant sequence matches with four known rheumatoid arthritis auto-antigens, there was a perfect match with one. In other conditions, they found:
Lupus erythematosus
- SmN: 53%
- SSA (Ro): 60%
- snRNP-SmD3: 64%
- SSB (La): 69%
- U2 snRNP B”: 83%
Heart disease
- P-selectin (protein on surface of blood vessels & platelets): 80%
- Myosin (involved with muscle contraction): 88%
- Intercellular adhesion molecule-1 (inflammatory response molecules): 100%
Anti-phospholipid syndrome
- β2-Glycoprotein-1 precursor: 56%
- Annexin A5: 63%
- Anti-CL/β-2GPI Ig light chain variable region: 73%
AIDs-associated antigens
- Thyroglubulin: 52%
- GAD65: 57%
- Zinc transporter 8: 57%
- Transglutaminase: 60%
- Thyroid peroxidase: 71%
- Soluble liver/pancreas antigen: 80%
- Calprotectin (protein S100-A8): 100%
Sclerosis-associated antigens
- Major centromere autoantigen B: 57%
- RNA polymerase III: 67%
- U3-snRNP fibrillarin: 75%
- U3-snRNP MPP10: 75%
- hU3-55kDA: 86%
- Nucleophosmin B23: 88%
A perfect match with a molecule may not be necessary to result in an autoimmune response, so percentages of less than 100% may not indicate lack of an autoimmune response. However, the closer the match between a molecule and an antigen, the more likely it is that an autoimmune response will occur.
Although you may not generally think of heart disease as an autoimmune disorder, certain forms of it, such as rheumatic heart disease, are known to be—and as this study seems to indicate, others may be, too.” (148)Included in Hep B (Engerix- B), Hep B (Recombivax), HPV( Gardasil), Pneumococcal (PCV13- Prevnar), Dtap+Hep B+IPV (Pediarix), Hib+Hep B (Comvax), Hep A+ Hep B (Twinrix), Meningococcal (MCV4-Menomune)
Vero cells- See monkey kidney cells
Vitamins- “Vitamins are organic compounds which are needed in small quantities to sustain life. We get vitamins from food, because the human body either does not produce enough of them, or none at all. An organic compound contains carbon. When an organism (living thing) cannot produce enough of an organic chemical compound that it needs in tiny amounts, and has to get it from food, it is called a vitamin.” (149)
Resources for above list
(5) http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=31236
(6)http://vaccinetruth.org/2-phenoxyethanol.htm
(7)http://www.google.com/patents/CA2333578A1?cl=en
(8)http://www.jimmunol.org/content/183/10/6186.full
(9)http://pubchem.ncbi.nlm.nih.gov/compound/vitamin_e_succinate#section=MeSH-Tree
(10)https://www.nrv.gov.au/nutrients/vitamin-e
(11)http://pediatric-orthopedics.com/Treatments/SDR_baclofen_OH/Alcohol/alcohol.html
(12)http://www.nlm.nih.gov/medlineplus/druginfo/meds/a699048.html#side-effects
(13)http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+691
(14)http://www.vitamins-supplements.org/amino-acids/
(15)http://www.nutritional-supplements-health-guide.com/amino-acid-side-effects.html
(16)http://www.aluminumsulfate.net/Ammonium-Sulfate.html
(17)http://www.violinet.org/vaxjo/vaxjo_detail.php?c_vaxjo_id=79
(18)https://explorevaccines.wordpress.com/2008/11/06/aluminum-in-vaccines-part-1/
(19)http://altmedicine.about.com/cs/herbsvitaminsad/a/Arginine.htm
(20)http://www.epa.gov/ttn/atw/hlthef/propiola.html
(21)http://www.biowest.net/products/serum/bovine-serum-albumin-bsa/
(23)http://www.nlm.nih.gov/medlineplus/druginfo/meds/a601032.html
(24)http://www.ima-na.org/?page=what_is_calcium_carb
(25)http://www.labome.com/method/Fetal-Bovine-Serum.html
(26)http://www.eufic.org/article/en/expid/basics-carbohydrates/
(27)http://www.definition-of.com/casamino%20acids
(28)http://www.wisegeek.org/what-is-casein.htm
(29)http://www.scq.ubc.ca/cell-culture/
(31)http://www.ncbi.nlm.nih.gov/pmc/articles/PMC377105/
(32)http://www.ncbi.nlm.nih.gov/pubmed/12673763
(33)http://www.atcc.org/~/media/B69BFB9F6EFB4BE597062BAD9359C632.ashx
(34)http://www.sigmaaldrich.com/life-science/biochemicals/biochemical-products.html?TablePage=104863014
(35)http://www.sailhome.org/Concerns/Vaccines.html
(38)http://www.ncbi.nlm.nih.gov/pubmed?cmd=retrieve&list_uids=17188501,15356194
(40)http://www.sigmaaldrich.com/life-science/biochemicals/biochemical-products.html?TablePage=22696471
(41)http://www.sugar.org/other-sweeteners/other-caloric-sweeteners/
(42)http://www.drugs.com/sfx/dextrose-side-effects.html
(43)http://everything2.com/title/dipotassium%2520phosphate
(44)http://www.drugs.com/sfx/potassium-phosphate-side-effects.html
(45)http://www.chemicalland21.com/lifescience/foco/DIMETHYL%20beta-CYCLODEXTRIN.htm
(46)http://tpx.sagepub.com/content/36/1/30.long
(47)http://www.ncbi.nlm.nih.gov/pubmed?cmd=retrieve&list_uids=9706061
(48)http://www.ncbi.nlm.nih.gov/pubmed/1732230
(49)http://www.sigmaaldrich.com/life-science/cell-culture/classical-media-salts/dmem.html
(50)http://himedialabs.com/TD/AL020.pdf
(51)http://www.phac-aspc.gc.ca/publicat/cig-gci/p02-04-eng.php
(52)http://umm.edu/health/medical/altmed/supplement/ethylenediaminetetraacetic-acid
(54)http://www.humaneresearch.org.au/campaigns/fetal_calf_serum
(55)Dr. Tenpenny's video what science and CDC documents revial
(56)http://www.formaldehydetesting.com/whatisformaldehyde.html
(57)http://www.cancer.gov/cancertopics/factsheet/risk/formaldehyde
(58)IARC 2006, Asian et al. 2006, Sarsilmaz et al. 2007, Golalipour et al. 2008, Ozen et al. 2005, Majumder and kumar 1995
(59)http://www.wisegeek.org/what-is-formalin.htm
(60)http://m.jem.rupress.org/content/6/4-6/487.abstract
(61)http://www.google.com/patents/WO1998054296A1?cl=en
(62)http://www.peta.org/about-peta/faq/what-is-gelatin-made-of/
(64)http://www.webmd.com/drugs/2/drug-94473/gentamicin-sulfate-pf-intravenous/details#precautions
(65)http://www.alsa.org/research/about-als-research/glutamate.html
(66)http://nj.gov/health/eoh/rtkweb/documents/fs/0960.pdf
(67)http://naples.cc.sunysb.edu/Admin/HRSForms.nsf/pub/EHSD0095/$FILE/EHSD0095.pdf
(68)http://www.drugs.com/cdi/hemin.html
(69)http://www.scbt.com/datasheet-202646-hemin-chloride.html
(70)http://nationalenzyme.com/education/what-are-enzymes/
(71)http://web.extension.illinois.edu/ethanol/
(72)http://www.drugs.com/sfx/albumin-human-side-effects.html
(73)http://www.immunizationinfo.org/issues/vaccine-components/human-fetal-links-some-vaccines
(74)http://collagenguide.net/hydrolyzed-collagen-side-effects
(75)http://www.ncbi.nlm.nih.gov/pubmed/21983546
(77)http://tools.lifetechnologies.com/content/sfs/manuals/insect_man.pdf
(81)http://www.bioind.com/page_14376
(82)http://www.elmhurst.edu/~chm/vchembook/546lactose.html
(83)http://www.freepatentsonline.com/6372225.html
(84)http://biology.clc.uc.edu/courses/bio104/lipids.htm
(85)https://www.lifetechnologies.com/order/catalog/product/31100019
(86)http://www.seppic.com/human-health/mineral-salts-@/1060/view-986-category.html
(87)http://www.sigmaaldrich.com/life-science/cell-culture/classical-media-salts/mem-media.html
(88)http://www.ncbi.nlm.nih.gov/pmc/articles/PMC357228/pdf/jbacter00552-0091.pdf
(89)http://mic.sgmjournals.org/content/63/2/211.full.pdf
(90)http://www.rxlist.com/boostrix-drug.htm
(91)The risks, the benefits, the choices by. Dr. Tenpenny
(92)http://micro.magnet.fsu.edu/primer/techniques/fluorescence/gallery/cells/vero/verocells.html
(93)http://www.ncbi.nlm.nih.gov/pmc/articles/PMC452549/
(94)http://www.medsafe.govt.nz/Profs/Datasheet/d/DBLPotassiumDihydrogeninj.pdf
(95)http://www.med-health.net/What-Is-Msg.html
(96)http://www.foodrenegade.com/msg-dangerous-science/
(97)http://micro.magnet.fsu.edu/primer/techniques/fluorescence/gallery/cells/mrc5/mrc5cells.html
(98)http://www.cbsnews.com/news/vaccines-and-autism-a-new-scientific-review/
(100)http://www.drugs.com/cdi/neomycin.html
(101)http://www.rxlist.com/neomycin-sulfate-drug.htm
(103)http://www.toxipedia.org/display/toxipedia/Nonylphenol+and+Nonylphenol+Ethoxylates
(104)http://apps.sepa.org.uk/spripa/Pages/SubstanceInformation.aspx?pid=156
(105)http://www.worthington-biochem.com/oa/default.html
(106)http://www.epa.gov/airtoxics/hlthef/phenol.html
(108)http://www.unl.edu/cahoonlab/phosphate%20buffer.pdf
(109)http://www.rxlist.com/polymyxin-b-drug/side-effects-interactions.htm
(110)http://teodorolab.mcgill.ca/Viral_Apoptosis.html
(111)http://hazmap.nlm.nih.gov/category-details?table=copytblagents&id=3617
(112)http://articles.mercola.com/sites/articles/archive/2014/03/22/aluminum-toxicity-alzheimers.aspx
(113)http://pubchem.ncbi.nlm.nih.gov/compound/potassium_chloride#section=2D-Structure
(114)http://www.scbt.com/datasheet-203211-potassium-phosphate-monobasic.html
(115)http://www.webmd.com/drugs/2/drug-63290/potassium-phosphate,-monobasic-oral/details#uses
(116)http://www.ncbi.nlm.nih.gov/pubmed/16400901
(117)http://www.drugs.com/sfx/darbepoetin-alfa-side-effects.html
(118)http://www.vaccine-tlc.org/human
(119)http://www.drugs.com/sfx/albumin-human-side-effects.html
(120)http://link.springer.com/article/10.1023%2FA%3A1008978903231
(121)http://www.ncbi.nlm.nih.gov/pubmed/6649955
(122)http://www.drugs.com/sfx/sodium-bicarbonate-side-effects.html
(123)http://chemistry.about.com/od/howthingsworkfaqs/a/howboraxworks.htm
(124)http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776007/
(125)http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+328
(126)http://www.medicinenet.com/sodium_citrate_alk_citric_acid-oral_liquid/page2.htm
(127)http://cancer.dartmouth.edu/pf/health_encyclopedia/d03952a1
(128)http://www.funakoshi.co.jp/data/datasheet/PCC/89904.pdf
(129)http://www.ncbi.nlm.nih.gov/pubmed/16905748
(130)http://www.ncbi.nlm.nih.gov/pubmed/17188501
(131)http://www.scbt.com/datasheet-251042-sodium-phosphate-monobasic-dihydrate.html
(132)http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+738
(133)http://www.nlm.nih.gov/medlineplus/ency/article/002487.htm
(134)http://www.ncbi.nlm.nih.gov/pubmedhealth/PMHT0012174/?report=details#side_effects
(135)http://pubchem.ncbi.nlm.nih.gov/compound/D-Sorbitol#section=Explosive-Limits-and-Potential
(136)http://www.sigmaaldrich.com/catalog/product/fluka/70178?lang=en®ion=US
(137)http://wellnessmama.com/3684/is-soy-healthy/
(138)http://www.drugs.com/cdi/streptomycin.html
(139)https://www.applichem.com/en/products/biochemica/biological-buffer/
(140)http://www.bio-world.com/productinfo/4_847_63_475/131083/Succinate-M-buffer-soln-pH.html
(141)http://www.elmhurst.edu/~chm/vchembook/546sucrose.html
(142)http://www.ncbi.nlm.nih.gov/pubmed/11331700
(144)http://old.env-health.org/IMG/pdf/mercury_chapter1.pdf
(145)http://www.immunize.org/concerns/vaticandocument.htm
(148)http://healthimpactnews.com/2013/yeast-in-vaccines-tied-to-autoimmune-diseases/
(149)http://www.medicalnewstoday.com/articles/195878.php
(150)http://childrenshealthchoices.org/cave.html
Medical diagnostic codes for vaccine injuries. Source - 2017 ICD-10-CM (Diagnostic coding manual). You can look them up for free here http://www.icd10data.com
Learn what diagnostic codes are here http://www.medicalbillingandcodingu.org/the-basics-of-icd-diagnosis-coding/
G04.02 - the medical diagnostic code for postimmunization acute disseminated encephalomyelitis (ADEM). An autoimmune disease marked by a sudden, widespread attack of inflammation in the brain and spinal cord.
G04.32 - the medical diagnostic code for postimmunization acute necrotizing hemorrhagic encephalopathy.
T80.52 - medical diagnostic code for anaphylactic reaction due to vaccination
T80.62 - medical diagnostic code for serum reaction due to vaccination
T88.0 - medical diagnostic code for sepsis following immunization
T88.1 - medical diagnostic code for generalized vaccinia/rash following immunization
M02.2 -medical diagnostic code section for postimmunization arthropathy
R50.83 -medical diagnostic code for postimmunization fever
T50.A - medical diagnostic code section for poisoning by, adverse effect of and underdosing of bacterial vaccines
T50.B - medical diagnostic code section for poisoning by, adverse effect of and underdosing of viral vaccines
T50.Z - medical diagnostic code section for poisoning by, adverse effect of and underdosing of other vaccines and biological substances
CONTRAINDICATION CHECKLIST
Doctors are supposed to have parents fill out this form before every set of childhood vaccinations but most do not.
This checklist plus more information on some contraindications can be found here:
http://www.immunize.org/catg.d/p4060.pdf
I found the above link on the cdc website here under "Screening Questionnaires: -for Child and Teen Immunization":
https://www.cdc.gov/vaccines/hcp/admin/recs-guidelines.html
See next two pages if you do not wish to download the above pdf but would like to save images of the form
Modified AAP Refusal of Vaccination Form
When declining vaccines, doctors will hand you a form to fill out stating that you are declining the vaccines. DO NOT sign this form as it contains self incrimination language (quote: “ ...I know that failure to follow the recommendations about vaccination may endanger the health or life of my child…”).
Instead, you may print out and use a modified vaccine refusal form which contains no self incrimination language . A copy of this modified form can be found through the following link or save the image from the following page in my document:
http://www.vaclib.org/exempt/files/AAPmodified.pdf
VACCINE PACKAGE INSERTS
All the vaccine inserts can be found here: http://www.immunize.org/packageinserts/
and here :http://www.vaccinesafety.edu/package_inserts.htm
ADVERSE REACTIONS (see package insert links and included images):
Infanrix - DTap - https://www.gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Infanrix/pdf/INFANRIX.PDF
Pediarix - DTaP+HepB+IPV - https://www.gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Pediarix/pdf/PEDIARIX.PDF
Hiberix - HIB - https://www.gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Hiberix/pdf/HIBERIX.PDF
Pedvax - HIB - http://www.merck.com/product/usa/pi_circulars/p/pedvax_hib/pedvax_pi.pdf
Havrix - Hep A - https://www.gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Havrix/pdf/HAVRIX.PDF
Twinrix - Hep a/Hep b - https://gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Twinrix/pdf/TWINRIX.PDF
Vaqta - Hep A - http://www.merck.com/product/usa/pi_circulars/v/vaqta/vaqta_pi.pdf
Engerix-b - Hep b - https://www.gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Engerix-B/pdf/ENGERIX-B.PDF
Flublok - flu - http://www.flublok.com/media/1009/18pluspackinsert-2016.pdf
Flulaval - flu - https://gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Flulaval_Quadrivalent/pdf/FLULAVAL-QUADRIVALENT.PDF
Flumist - flu - http://www.azpicentral.com/flumistquadrivalent/flumistquadrivalent.pdf#page=1
Fluvirin - flu - http://flu.seqirus.com/assets/files/us%20package%20insert_fluvirin%202015-2016.pdf
Fluzone high dose - flu - https://www.vaccineshoppe.com/image.cfm?pi=fluHD&image_type=product_pdf
Fluzone intradermal - flu - https://www.vaccineshoppe.com/image.cfm?pi=IDQIV&image_type=product_pdf
Fluzone Quadrivalent - flu - https://www.vaccineshoppe.com/image.cfm?pi=fluQIV&image_type=product_pdf
MMR II - measles, mumps, rubella - http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf
ProQuad - MMRV measles, mumps, rubella and varicella - http://www.merck.com/product/usa/pi_circulars/p/proquad/proquad_pi.pdf
Menactra - Meningococcal - https://www.vaccineshoppe.com/image.cfm?doc_id=12580&image_type=product_pdf
Menhibrix - meningococcal - https://gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Menhibrix/pdf/MENHIBRIX.PDF
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IPOL - polio - https://www.vaccineshoppe.com/image.cfm?doc_id=5984&image_type=product_pdf
Kinrix - Dtap/IPV - https://www.gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Kinrix/pdf/KINRIX.PDF
Pentacel - Dtap/IPV/Hib - https://www.vaccineshoppe.com/image.cfm?doc_id=11169&image_type=product_pdf
Quadracel - Dtap/IPV - https://www.vaccineshoppe.com/image.cfm?doc_id=12924&image_type=product_pdf
Rotarix - Rotavirus - https://www.gsksource.com/pharma/content/dam/GlaxoSmithKline/US/en/Prescribing_Information/Rotarix/pdf/ROTARIX-PI-PIL.PDF
Rotateq - Rotavirus - http://www.merck.com/product/usa/pi_circulars/r/rotateq/rotateq_pi.pdf
Varivax - Vericella - http://www.merck.com/product/usa/pi_circulars/v/varivax/varivax_pi.pdf
VACCINES LINKED TO EAR INFECTIONS (OTITIS MEDIA)
MMR: https://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf
Rotavirus: http://www.merck.com/product/usa/pi_circulars/r/rotateq/rotateq_pi.pdf
Fact sheet pertaining to mandatory vaccines ( see next image or click on link ) http://www.aapsonline.org/testimony/mandvac.htm
from the Journal of American Physicians and Surgeons:
"Although CDC recommends polio, hepatitis B, diphtheria, tetanus, pertussis, rotavirus, Haemophilus in uenzae type B, and pneumococcal vaccines for two-, four-, and six-month-old infants, this combination of eight vaccines administered during a single physician visit was never tested for safety in clinical trials. This is at odds with a CDC report that found that mixed exposures to chemical substances and other stress factors, including prescribed pharmaceuticals, may produce “increased or unexpected deleterious health e ects.” This CDC report also noted that “exposures to mixed stressors can produce health consequences that are additive, synergistic, antagonistic, or can potentiate the response expected from individual component exposures.”12 Thus, CDC is well aware that mixing several pharmaceutical products increases the likelihood of synergistic toxicity and unexpected adverse reactions....."
Also states-
" Our study showed that infants who receive several vaccines concurrently, as recommended by CDC, are significantly more likely to be hospitalized or die when compared with infants who receive fewer vaccines simultaneously. It also showed that reported adverse effects were more likely to lead to hospitalization or death in younger infants.
These findings are so troubling that we expected major media outlets in America to sound an alarm, calling for an immediate reevaluation of current preventive health care practices. But 4 years after publication of our study, this has not happened."
www.jpands.org/vol21no2/miller.pdf
"A review suggested that it took an average of 17 years for 14% of original (i.e., discovery) research to be integrated into physician practice." - ncbi.nlm.nih.gov/pmc/articles/PMC1497798/
National Vaccine Injury Compensation Program Statistics Report
http://www.hrsa.gov/vaccinecompensation/statisticsreport.pdf
"Nations that require more vaccines tend to have higher infant mortality rates"
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/
1000 peer review studies proving vaccines aren't safe
https://drive.google.com/file/d/0B3mMkPwF1DUPckVEZ2JkMXV2ams/view
"There is no Federal requirement for informed consent relating to immunization." http://www.cdc.gov/vaccines/imz-managers/laws/
"Nations that require more vaccines tend to have higher infant mortality rates"
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/
Pediatricians receive large bonuses for having most of their patients up to date in vaccines before a certain age (see image below). Source: http://web.archive.org/web/20160705063350/http://thephysicianalliance.org/wp-content/uploads/2016/03/2016-BCN-BCBSM-Incentive-Program-Booklet.pdf
John Hopkins hospital warns that the immunocompromised (people with weak immune systems) should avoid contact with recently vaccinated individuals (see next image):
St. Judes childrens hospital warns that vaccinated individuals are a threat to the immunocompromised (see next image)
ECZEMA VACCINATUM
Abstract
Nine cases of eczema vaccinatum are presented, including two fatalities. Seven were caused by contact of a child with eczema with a recently vaccinated sibling.
Suddenly appearing umbilicated vesicles superimposed upon atopic eczema are almost diagnostic of eczema vaccinatum or eczema herpeticum. These do not occur with mere secondary bacterial infection.
Hyperimmune vaccinal gamma-globulin is now available for specific therapy.
Eczema vaccinatum is frequently iatrogenic and uniformly preventable.
The following steps are recommended for prophylaxis: 1) No child with atopic eczema or other skin disorder should be vaccinated. 2) No child should be vaccinated if any member of his family has eczema or other skin disorder. 3) Parents of children with eczema should be notified at the onset of the disease of the danger from vaccination contact. 4) If a sibling of a child with atopic eczema is vaccinated, he must be completely separated from that child for at least 21 days. 5) Forms used by state and local health departments for parents' consent to vaccination should include an appropriate warning of the contraindications. 6) Eczema vaccinatum should be a reportable disease. 7) Patients recently vaccinated must be excluded from pediatric wards containing patients with atopic eczema, other diseases of the skin, burns or healing surgical incisions. 8) Vaccination may be recommended at 2 months of age, especially for babies from strongly allergic families.
http://pediatrics.aappublications.org/content/22/2/259
Aluminum is in the following vaccines given to minors:
DTaP, Pediarix (DTaP-Hepatitis B-Polio combination), Pentacel (DTaP-HIB-Polio combination), Hepatitis A, Hepatitis B, Haemophilus influenzae B (HIB), Human Papilloma Virus (HPV), and Pneumococcal vaccines
INGESTION VS INJECTION
"In healthy subjects, only 0.3% of orally administered aluminum is absorbed via the GI tract, and the kidneys effectively eliminate aluminum from the human body. Only when the GI barrier is bypassed, such as by intravenous infusion or in the presence of advanced renal dysfunction, does aluminum have the potential to accumulate. As an example, with intravenously infused aluminum, 40% is retained in adults and up to 75% is retained in neonates.[4]"
"If a significant aluminum load exceeds the body's excretory capacity, the excess is deposited in various tissues, including bone, brain, liver, heart, spleen, and muscle. This accumulation causes morbidity and mortality through various mechanisms.[2]"
http://emedicine.medscape.com/article/165315-overview
"In adults, aluminum exposure can lead to apparently age-related neurological deficits resembling Alzheimer's and has been linked to this disease and to the Guamanian variant, ALS-PDC. Similar outcomes have been found in animal models. In addition, injection of aluminum adjuvants in an attempt to model Gulf War syndrome and associated neurological deficits leads to an ALS phenotype in young male mice.
In young children, a highly significant correlation exists between the number of pediatric aluminum-adjuvanted vaccines administered and the rate of autism spectrum disorders. Many of the features of aluminum-induced neurotoxicity may arise, in part, from autoimmune reactions, as part of the ASIA syndrome."
http://www.ncbi.nlm.nih.gov/m/pubmed/23609067/
Abstract
"Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of aluminum (Al) adjuvants through routine vaccinations. According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic. Taken together, these observations raise plausible concerns about the overall safety of current childhood vaccination programs. When assessing adjuvant toxicity in children, several key points ought to be considered: (i) infants and children should not be viewed as "small adults" with regard to toxicological risk as their unique physiology makes them much more vulnerable to toxic insults; (ii) in adult humans Al vaccine adjuvants have been linked to a variety of serious autoimmune and inflammatory conditions (i.e., "ASIA"), yet children are regularly exposed to much higher amounts of Al from vaccines than adults; (iii) it is often assumed that peripheral immune responses do not affect brain function. However, it is now clearly established that there is a bidirectional neuro-immune cross-talk that plays crucial roles in immunoregulation as well as brain function. In turn, perturbations of the neuro-immune axis have been demonstrated in many autoimmune diseases encompassed in "ASIA" and are thought to be driven by a hyperactive immune response; and (iv) the same components of the neuro-immune axis that play key roles in brain development and immune function are heavily targeted by Al adjuvants. In summary, research evidence shows that increasing concerns about current vaccination practices may indeed be warranted. Because children may be most at risk of vaccine-induced complications, a rigorous evaluation of the vaccine-related adverse health impacts in the pediatric population is urgently needed."
http://www.ncbi.nlm.nih.gov/m/pubmed/22235057/
The development of rheumatoid arthritis after recombinant hepatitis B vaccination.
CONCLUSION: These polymorphic residues in the binding site of the MHC class II molecules of the affected patients appear capable of binding some peptide sequences of the recombinant vaccine peptides they received and may be responsible for hepatitis B vaccine triggering development of RA in these cases. Recombinant hepatitis B vaccine may trigger the development of RA in MHC class II genetically susceptible individuals.
https://www.ncbi.nlm.nih.gov/m/pubmed/9733447/
A one year followup of chronic arthritis following rubella and hepatitis B vaccination based upon analysis of the Vaccine Adverse Events Reporting System (VAERS) database.
CONCLUSION: This study revealed that adult rubella and adult hepatitis B vaccines were statistically associated with chronic arthritis which persisted for at least one year. The etiology for these adverse reactions may involve autoimmune mechanisms. Furthermore, potential biases in the reporting rates of adverse reactions to VAERS were not observed.
https://www.ncbi.nlm.nih.gov/m/pubmed/12508767/
"Anxiety-like behavior was more pronounced among mice immunized with alum. In conclusion, herein we report that immunization with the HBVv (hepatitis b vaccine) aggravated kidney disease in an animal model of SLE. Immunization with either HBVv or alum affected blood counts, neurocognitive functions and brain gliosis. Our data support the concept that different component of vaccines may be linked with immune and autoimmune mediated adverse events."
http://www.ncbi.nlm.nih.gov/m/pubmed/25042822/
Recombinant hepatitis B vaccine and the risk of multiple sclerosis: a prospective study.
CONCLUSIONS: These findings are consistent with the hypothesis that immunization with the recombinant hepatitis B vaccine is associated with an increased risk of MS, and challenge the idea that the relation between hepatitis B vaccination and risk of MS is well understood.
https://www.ncbi.nlm.nih.gov/m/pubmed/15365133/
Postvaccinal inflammatory neuropathy: peripheral nerve biopsy in 3 cases
Abstract
Autoimmune inflammatory polyneuropathy (PN) can be triggered by vaccination. We report 3 such cases. A 36-year-old female nurse presented 15 days after a hepatitis B vaccination (HBV) with acute sensory disturbances in the lower limbs. She had severe ataxia but no weakness. Cerebrospinal fluid (CSF) protein level was 84 mg/100 mL, with 3 lymphocytes. A 66-year-old man presented 21 days after HBV with severe motor and sensory PN involving all 4 limbs. A 66-year-old man presented 15 days after a yellow fever vaccination with progressive motor and sensory PN involving all 4 limbs and bilateral facial paralysis. CSF protein level was 300 mg/100 mL, with 5 lymphocytes. Six weeks later, a tracheostomy was performed. In these 3 patients, the nerve deficits lasted for months. In each case, peripheral nerve biopsy showed KP1-positive histiocytes but no T-lymphocytes in the endoneurium. On ultrastructural examination, there was axonal degeneration in the first 2 cases; in case 2, a few myelinated fibers exhibited an intra-axonal macrophage but the myelin sheath was preserved. There was only 1 example of macrophage-associated demyelination in case 2, but these were numerous in case 3. It is likely that in the first 2 cases, an autoimmune reaction against some axonal or neuronal components was triggered by HBV. It induced an acute sensory ataxic PN in case 1 and an acute motor and sensory axonal neuropathy (AMSAN) in case 2. The third patient had a chronic inflammatory demyelinating PN, likely triggered by yellow fever vaccination.
https://www.ncbi.nlm.nih.gov/pubmed/12365564
A one year followup of chronic arthritis following rubella and hepatitis B vaccination based upon analysis of the Vaccine Adverse Events Reporting System (VAERS) database.
CONCLUSION:
This study revealed that adult rubella and adult hepatitis B vaccines were statistically associated with chronic arthritis which persisted for at least one year. The etiology for these adverse reactions may involve autoimmune mechanisms. Furthermore, potential biases in the reporting rates of adverse reactions to VAERS were not observed
https://www.ncbi.nlm.nih.gov/pubmed/12508767
Adverse events associated with hepatitis B vaccine in U.S. children less than six years of age, 1993 and 1994.
RESULTS:
Controlling for age, race, and gender simultaneously in the 1994 NHIS, hepatitis B vaccine was found to be associated with prevalent arthritis [odds ratio (OR) = 5.91, 95% confidence interval (CI) = 1.05-33.14], incident acute ear infections (OR = 1.60, 95% CI = 1.00-2.58), and incident pharyngitis/nasopharyngitis (OR = 1.41, 95% CI = 0.95-2.09).
CONCLUSIONS:
Evidence from this study suggests that hepatitis B vaccine is positively associated with adverse health outcomes in the general population of US children.
https://www.ncbi.nlm.nih.gov/pubmed/11164115
Aluminum hydroxide (which is in vaccines) injections lead to motor deficits and motor neuron degeneration
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819810/
Long-term persistence of vaccine-derived aluminum hydroxide is associated with chronic cognitive dysfunction.
Abstract
Macrophagic myofasciitis (MMF) is an emerging condition, characterized by specific muscle lesions assessing long-term persistence of aluminum hydroxide within macrophages at the site of previous immunization. Affected patients mainly complain of arthromyalgias, chronic fatigue, and cognitive difficulties. We designed a comprehensive battery of neuropsychological tests to prospectively delineate MMF-associated cognitive dysfunction (MACD). Compared to control patients with arthritis and chronic pain, MMF patients had pronounced and specific cognitive impairment. MACD mainly affected (i) both visual and verbal memory; (ii) executive functions, including attention, working memory, and planning; and (iii) left ear extinction at dichotic listening test. Cognitive deficits did not correlate with pain, fatigue, depression, or disease duration. Pathophysiological mechanisms underlying MACD remain to be determined. In conclusion, long-term persistence of vaccine-derived aluminum hydroxide within the body assessed by MMF is associated with cognitive dysfunction, not solely due to chronic pain, fatigue and depression.
https://www.ncbi.nlm.nih.gov/pubmed/19748679
Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice.
"Aluminum-treated groups also showed significant motor neuron loss (35%) and increased numbers of astrocytes (350%) in the lumbar spinal cord. The findings suggest a possible role for the aluminum adjuvant in some neurological features associated with GWI and possibly an additional role for the combination of adjuvants."
http://www.ncbi.nlm.nih.gov/pubmed/17114826
" By applying Hill's criteria for establishing causality between exposure and outcome we investigated whether exposure to Al (aluminum) from vaccines could be contributing to the rise in ASD (autism spectrum disorders) prevalence in the Western world. Our results show that: (i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades"
http://www.ncbi.nlm.nih.gov/pubmed/22099159
How aluminum, an intracellular ROS generator promotes hepatic and neurological diseases: the metabolic tale
"Metal pollutants are a global health risk due to their ability to contribute to a variety of diseases. Aluminum (Al), a ubiquitous environmental contaminant is implicated in anemia, osteomalacia, hepatic disorder, and neurological disorder. In this review, we outline how this intracellular generator of reactive oxygen species (ROS) triggers a metabolic shift towards lipogenesis in astrocytes and hepatocytes. This Al-evoked phenomenon is coupled to diminished mitochondrial activity, anerobiosis, and the channeling of α-ketoacids towards anti-oxidant defense. The resulting metabolic reconfiguration leads to fat accumulation and a reduction in ATP synthesis, characteristics that are common to numerous medical disorders. Hence, the ability of Al toxicity to create an oxidative environment promotes dysfunctional metabolic processes in astrocytes and hepatocytes. These molecular events triggered by Al-induced ROS production are the potential mediators of brain and liver disorders.”
http://link.springer.com/article/10.1007%2Fs10565-013-9239-0
"Repeated immunization with antigen causes systemic autoimmunity in mice otherwise not prone to spontaneous autoimmune diseases. Overstimulation of CD4 + T cells by repeated immunization with antigen led to the development of a fully-matured autoantibody-inducing CD4 + T (aiCD4 + T) cell which had undergone T cell receptor (TCR) revision and was capable of inducing autoantibodies. The aiCD4 + T cell was induced by de novo TCR revision but not by cross-reaction to immunizing antigen, and subsequently overstimulated CD8 + T cells, driving them to become MHC class I-restricted, antigen-specific cytotoxic T lymphocytes (CTL). These CTLs could be further matured by antigen cross-presentation, after which they caused autoimmune tissue injury akin to systemic lupus erythematosus (SLE). Autoimmune tissue injury did not appear in CD8 + T cell-deficient mice. Further, inhibition of antigen-cross presentation by treating with chloroquine abrogated the generation of CTL and autoimmune tissue injury."
Conclusion:
"Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s immune ‘system’ by repeated immunization with antigen, to the levels that surpass system’s self-organized criticality."
http://www.jimmunol.org/cgi/content/meeting_abstract/184/1_MeetingAbstracts/93.39
Autoimmunity and non-accidental injury in children
Abstract:
"Background: The Shaken Baby Syndrome conceived by Guthkeltch to explain bruises, fractures, retinal and cerebral haemorrhage and encephalopathy in children, called the “triad”, can be explained by an autoimmune reaction to antigens in a genetically susceptible child. Method: Children diagnosed as suffering from Non-accidental injuries were investigated for evidence of immune response reactions following mandated vaccination and childhood illnesses. Results: It was found in all the cases reported here the response to antigenic stimulation damaged the Beta cells in the Pancreas causing Hypoinsulinaemia which inhibited the cellular uptake of Vitamin C resulting in liver dysfunction, failure of carboxylation of the Vitamin K dependent proteins resulting in haemorrhages and fractures associated with the “triad”. Conclusion: Fractures, retinal and subdural haemorrhages and encephalopathy in children – is an autoimmune response to antigenic stimulation in a genetically susceptible individual. Common antigens are the mandated vaccines, viral bacterial and parasitic infections. "
Interpretation
"In all four cases shown here there is evidence that hyperglycaemia followed vaccination and hyperglycaemia implies hypoinsulinism, an autoimmune disorder resulting from the destruction of the Beta cells of the pancreas. Since insulin is required for the transfer of vitamin C into the cells the intracellular vitamin C is reduced[12]. The resulting “tissue scurvy” compromises the function of the Liver by inhibiting carboxylation of the clotting and bone forming factors and is manifested as the signs and symptoms of the “triad”. Both Dr Kalokerinos and Professor Clemetson recommended giving the infant Vitamin C before vaccination but it would seem more appropriate to do an intradermal skin test to test for sensitivity in every case. Both were firmly of the view that a metabolic abnormality of Vitamin C was the essential cause of the signs and symptoms of the alleged “Non-accidental injuries”. "
Michael D Innis. Autoimmunity and Non-Accidental Injury in Children. Clinical Medicine Research. Vol. 2, No. 3, 2013, pp. 40-44. doi: 10.11648/j.cmr.20130203.15
http://article.sciencepublishinggroup.com/pdf/10.11648.j.cmr.20130203.15.pdf
Encephalitis
"Encephalitis is inflammation of the brain that occurs when a virus directly infects the brain or when a virus, vaccine, or something else triggers inflammation. The spinal cord may also be involved, resulting in a disorder called encephalomyelitis."
" Encephalitis can occur in the following ways:
A virus directly infects the brain. A virus that caused an infection in the past becomes reactivated and directly damages the brain. A virus or vaccine triggers a reaction that makes the immune system attack brain tissue (an autoimmune reaction)."
" Autoimmune encephalitis: After certain viral infections or vaccines, the body's immune system sometimes attacks the layers of tissue that wrap around nerve fibers (called the myelin sheath) in the brain and spinal cord The attack occurs because proteins in myelin resemble those in the virus. As a result, nerve transmission becomes very slow. The resulting disorder, called acute disseminated encephalomyelitis, resembles multiple sclerosis except that symptoms do not come and go as they do in multiple sclerosis. The viruses most often involved include enteroviruses, Epstein-Barr virus, hepatitis A or B virus, human immunodeficiency virus (HIV), and influenza viruses."
The common immunogenic etiology of chronic fatigue syndrome: from infections to vaccines via adjuvants to the ASIA syndrome.
Abstract:
Chronic fatigue syndrome (CFS) is characterized by unexplained fatigue that lasts for at least 6 months with a constellation of other symptoms. Most cases start suddenly, and are usually accompanied by a flu-like illness. It is a symptom-based diagnosis of exclusion, the pathogenesis of which is unknown. Studies have examined and hypothesized about the possible biomedical and epidemiologic characteristics of the disease, including genetic predisposition, infections, endocrine abnormalities, and immune dysfunction and psychological and psychosocial factors. Recently, the AISA (autoimmune/inflammatory syndrome induced by adjuvants) syndrome was recognized, indicating the possible contribution of adjuvants and vaccines to the development of autoimmunity.
http://www.ncbi.nlm.nih.gov/pubmed/22054760
Review of Vaccine Induced Immune Overload and the Resulting Epidemics of Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent Accelerations in the Risk of Prediabetes and other Immune Mediated Diseases
Abstract
"There has been an epidemic of inflammatory diseases that has paralleled the epidemic on iatrogenic immune stimulation with vaccines. Extensive evidence links vaccine induced immune over load with the epidemic of type 1 diabetes. More recent data indicates that obesity, type 2 diabetes and other components of metabolic syndrome are highly associated with immunization and may be manifestations of the negative feedback loop of the immune system reacting to the immune overload. The epidemic of diabetes/prediabetes appears to be accelerating at a time when the prevalence of obesity has stabilized, indicating that the negative feedback system of the immune system has been over whelmed. The theory of vaccine induced immune overload can explain the key observations that have confounded many competing hypothesis. The current paper reviews the evidence that vaccine induced immune overload explains the disconnect between the increase in prediabetes and nonalcoholic fatty liver at a time when the obesity epidemic is waning in children."
"There are significantly elevated risks of primarily emergency room visits approximately one to two weeks following 12 and 18 month vaccination. Future studies should examine whether these events could be predicted or prevented"
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236196/
Influenza: marketing vaccine by marketing disease
Closer examination of influenza vaccine policies shows that although proponents employ the rhetoric of science, the studies underlying the policy are often of low quality, and do not substantiate officials’ claims. The vaccine might be less beneficial and less safe than has been claimed, and the threat of influenza appears overstated.
http://www.bmj.com/content/346/bmj.f3037
We randomized 115 children to trivalent inactivated influenza vaccine (TIV) or placebo. Over the following 9 months, TIV recipients had an increased risk of virologically-confirmed non-influenza infections (relative risk: 4.40; 95% confidence interval: 1.31-14.8). Being protected against influenza, TIV recipients may lack temporary non-specific immunity that protected against other respiratory viruses.
http://cid.oxfordjournals.org/content/54/12/1778.long
Effectiveness of trivalent inactivated influenza vaccine in influenza-related hospitalization in children: a case-control study.
“Using the Cochran-Mantel-Haenszel test for asthma status stratification, there was a significant association between hospitalization in asthmatic subjects and TIV (p = 0.001). TIV did not provide any protection against hospitalization in pediatric subjects, especially children with asthma. On the contrary, we found a threefold increased risk of hospitalization in subjects who did get the TIV vaccine. This may be a reflection not only of vaccine effectiveness but also the population of children who are more likely to get the vaccine.”
http://www.ncbi.nlm.nih.gov/pubmed/22525386
" The FluMist influenza vaccine strains replicate in the nasopharynx and can be recovered and cultured from respiratory secretions of vaccinated individuals (shed). The pattern and duration of shedding is important to understand because with prolonged shedding at high titer there is a theoretical risk of loss of attenuated phenotype, reassortment with wild-type influenza virus during influenza season, and transmission of vaccine virus to unvaccinated people, some of whom may be immunocompromised and/or at risk for complications of live viral infections."
"In each age group, among subjects who shed, shedding was most often observed on days 2-3 post vaccination. Among the population for whom FluMist is currently approved for use, i.e., individuals 2-49 years of age (n = 443), vaccine virus titers did not exceed 1.5 log10 TCID50/mL after day 11, though some individuals shed vaccine strain virus as late as day 28 post-vaccination. "
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM259175.pdf
Clustering of cases of insulin dependent diabetes (IDDM) occurring three years after hemophilus influenza B (HiB) immunization support causal relationship between immunization and IDDM.
http://www.ncbi.nlm.nih.gov/pubmed/12911277
CONCLUSION:
"We documented here the evidence of the potential of the HPV vaccine to trigger a life-disabling autoimmune condition. The increasing number of similar reports of post HPV vaccine-linked autoimmunity and the uncertainty of long-term clinical benefits of HPV vaccination are a matter of public health that warrants further rigorous inquiry."
http://www.ncbi.nlm.nih.gov/m/pubmed/23902317/
Conclusions:
"These findings are consistent with the hypothesis that immunization with the recombinant hepatitis B vaccine is associated with an increased risk of MS, and challenge the idea that the relation between hepatitis B vaccination and risk of MS is well understood."
http://www.neurology.org/content/63/5/838.abstract
Conclusions:
"Hepatitis B vaccination does not generally increase the risk of CNS inflammatory demyelination in childhood. However, the Engerix B vaccine appears to increase this risk, particularly for confirmed multiple sclerosis, in the longer term. Our results require confirmation in future studies."
http://www.ncbi.nlm.nih.gov/pubmed/18843097
" A majority of the ophthalmological complications seen following hepatitis B vaccination consist of vision loss, optic neuritis, papillary edema, uveitis, acute placoid pigment epitheliopathy and central vein occlusion. We present a 9-year-old girl who was referred to our hospital with decrease in vision and pain in the left eye a week after hepatitis B vaccination. A diagnosis of vaccine-induced optic neuritis was made."
http://www.ncbi.nlm.nih.gov/pubmed/19948437
Conclusions:
Children vaccinated in infancy are at increased risk of hepatitis B virus infection in the late teens
http://www.bmj.com/content/325/7364/569
"Acquired autoimmunity syndromes occur after viral vaccinations. Molecular mimicry is involved in these phenomena as is the necessity for the presence of two chemically complimentary antigens and an immunologic adjuvant. The HLA pattern of the host is also an important factor. The example used to explain these phenomena is demyelinating disease that follows hepatitis B vaccination. The somatic antigen of the hepatitis B virus in the vaccine has chemical complimentarity with the Epstein-Barr virus antigen in the vaccine recipient. The Epstein-Barr virus shows molecular mimicry with human myelin. The immunologic adjuvant is either present in the vaccine or muramyl peptides in the individual who is vaccinated. Why more than one type of autoimmune disease occurs is explained by the fact that specific autoimmune T-cells have been shown to develop clones that attack multiple human tissues."
http://www.ncbi.nlm.nih.gov/pubmed/17630224
*
According to the CDC the greatest reported complication is loose stool with measles.
Measles Complications Conditions Diarrhea - 8% reported
Otitis media - 7% reported
Pneumonia - 6% reported
Encephalitis - 0.1% reported
Seizures - 0.6-0.7% reported
Death - 0.2% reported
http://www.cdc.gov/vaccines/pubs/pinkbook/meas.html
The measles mortality rate had already dropped by over 98% before the vaccine was even introduced.
Thanks to better nutrition and hygiene, the death rate was LESS THAN 1 in 100,000 before the measles vaccine came out.
http://business.financialpost.com/2014/04/16/lawrence-solomon-the-untold-story-of-measles/
Waning of Maternal Antibodies Against Measles, Mumps, Rubella, and Varicella in Communities With Contrasting Vaccination Coverage
"Conclusions: Children of mothers vaccinated against measles and, possibly, rubella have lower concentrations of maternal antibodies and lose protection by maternal antibodies at an earlier age than children of mothers in communities that oppose vaccination. This increases the risk of disease transmission in highly vaccinated populations."
http://jid.oxfordjournals.org/content/early/2013/04/29/infdis.jit143.full
Measles inclusion-body encephalitis caused by the vaccine strain of measles virus.
Abstract
We report a case of measles inclusion-body encephalitis (MIBE) occurring in an apparently healthy 21-month-old boy 8.5 months after measles-mumps-rubella vaccination. He had no prior evidence of immune deficiency and no history of measles exposure or clinical disease. During hospitalization, a primary immunodeficiency characterized by a profoundly depressed CD8 cell count and dysgammaglobulinemia was demonstrated. A brain biopsy revealed histopathologic features consistent with MIBE, and measles antigens were detected by immunohistochemical staining. Electron microscopy revealed inclusions characteristic of paramyxovirus nucleocapsids within neurons, oligodendroglia, and astrocytes. The presence of measles virus in the brain tissue was confirmed by reverse transcription polymerase chain reaction. The nucleotide sequence in the nucleoprotein and fusion gene regions was identical to that of the Moraten and Schwarz vaccine strains; the fusion gene differed from known genotype A wild-type viruses.
https://www.ncbi.nlm.nih.gov/m/pubmed/10589903/
Fulminant encephalitis associated with a vaccine strain of rubella virus.
Abstract
Involvement of the central nervous system is common in measles, but rare in rubella. However, rubella virus (RV) can cause a variety of central nervous system syndromes, including meningitis, encephalitis, Guillain-Barré syndrome and sub acute sclerosing panencephalitis. We report the occurrence of one fatal case of the encephalitis associated with measles-rubella (MR) vaccine during an immunization campaign in São Paulo, Brazil. A 31 year-old-man, previously in good health, was admitted at emergency room, with confusion, agitation, inability to stand and hold his head up. Ten days prior to admission, he was vaccinated with combined MR vaccine (Serum Institute of India) and three days later he developed 'flu-like' illness with fever, myalgia and headache. Results of clinical and laboratory exams were consistent with a pattern of viral encephalitis. During hospitalization, his condition deteriorated rapidly with tetraplegia and progression to coma. On the 3rd day of hospitalization he died. Histopathology confirmed encephalitis and immunohistochemistry was positive for RV on brain tissue. RV was also detected by qPCR and virus isolation in cerebrospinal fluid, brain and other clinical samples. The sequence obtained from the isolated virus was identical to that of the RA 27/3 vaccine strain.
https://www.ncbi.nlm.nih.gov/m/pubmed/24216323/
Abstract
An outbreak of nine cases of mumps was reported from a total of 97 vaccinated nursing students at two medical colleges in Thailand in 2010, 16-26 days after administration of MMR vaccine containing the L-Zagreb mumps strain. Symptoms ranged in severity from fever and parotid swelling to orchitis. Clinical samples were obtained from seven patients and three were suitable for further study. Sequencing confirmed that the SH gene of the mumps virus in the unpassaged clinical specimens was identical to the L-Zagreb SH gene in the vaccine. Further analysis of the viral genome identified nucleotide position 5170 as a novel mutation which corresponds to an amino acid change in the fusion protein. This study provides another virologically confirmed example of mumps resulting from the L-Zagreb vaccine strain.
http://www.ncbi.nlm.nih.gov/pubmed/23089079
Aseptic meningitis as a complication of mumps vaccination.
Abstract
In 1989 a nationwide surveillance of neurologic complications after the administration of mumps vaccine was conducted in Japan, based on the notification of cases and the testing of mumps viruses isolated from cerebrospinal fluid for their relatedness to the vaccine by nucleotide sequence analysis. Among 630,157 recipients of measles-mumps-rubella trivalent (MMR) vaccine containing the Urabe Am9 mumps vaccine, there were at least 311 meningitis cases suspected to be vaccine-related. In 96 of these 311 cases, mumps virus related to the vaccine was isolated from cerebrospinal fluid. The unusually high incidence may have been partly a result of the adverse media publicity of the problem at the time of surveillance. We analyzed clinical features of 165 and 27 laboratory-confirmed mumps vaccine-related meningitis cases that occurred among the recipients of MMR and monovalent mumps vaccines, respectively, during a 1-year period after the introduction of MMR vaccine. The incidence of vaccine-related meningitis was similar among the recipients of MMR and monovalent Urabe Am9 mumps vaccines. Meningitis was generally mild and there were no sequelae from the illness. The complication was more frequent among male than among female children.
https://www.ncbi.nlm.nih.gov/m/pubmed/2041668/
POLIO: Symptoms
Symptoms
Most people who get infected with poliovirus (about 72 out of 100) will not have any visible symptoms.
About 1 out of 4 people with poliovirus infection will have flu-like symptoms that may include—
•Sore throat
•Fever
•Tiredness
•Nausea
•Headache
•Stomach pain
These symptoms usually last 2 to 5 days then go away on their own
A smaller proportion of people with poliovirus infection will develop other more serious symptoms - http://www.cdc.gov/polio/about/index.htm
Limited and localized outbreak of newly emergent type 2 vaccine-derived poliovirus in sichuan, china.
http://www.ncbi.nlm.nih.gov/pubmed/24850620
“Furthermore, while India has been polio-free for a year, there has been a huge increase in non-polio acute flaccid paralysis (NPAFP). In 2011, there were an extra 47,500 new cases of NPAFP. Clinically indistinguishable from polio paralysis but twice as deadly, the incidence of NPAFP was directly proportional to doses of oral polio received. Though this data was collected within the polio surveillance system, it was not investigated.”
http://www.ncbi.nlm.nih.gov/pubmed/22591873
"Oral poliovirus vaccine Trivalent OPV contains live attenuated strains of all three serotypes of poliovirus in a 10:1:3 ratio. The vaccine viruses are grown in monkey kidney tissue culture (Vero cell line). The vaccine is supplied as a single 0.5-mL dose in a plastic dispenser. The vaccine contains trace amounts of neomycin and streptomycin. OPV does not contain a preservative.
Live attenuated polioviruses replicate in the intestinal mucosa and lymphoid cells and in lymph nodes that drain the intestine. Vaccine viruses are excreted in the stool of the vaccinated person for up to 6 weeks after a dose. Maximum viral shedding occurs in the first 1–2 weeks after vaccination, particularly after the first dose.
Vaccine viruses may spread from the recipient to contacts. Persons coming in contact with fecal material of a vaccinated person may be exposed and infected with vaccine virus."
http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/polio.pdf
Breast milk makes rotavirus vaccine less effective
http://www.ncbi.nlm.nih.gov/pubmed/20442687
"We examined fecal shedding of pentavalent rotavirus vaccine (RV5) for 9 days following the first dose of vaccine in infants between 6 and 12 weeks of age. Rotavirus antigen was detected by enzyme immunoassay (EIA), and vaccine-type rotavirus was identified by nucleotide sequencing based on genetic relatedness to the RV5 VP6 gene. Stool from 22 (21.4%) of 103 children contained rotavirus antigen-positive specimens on ≥ 1 post-vaccination days. Rotavirus antigen was detected as early as post-vaccination day 3 and as late as day 9, with peak numbers of shedding on post-vaccination days 6 through 8. Vaccine-type rotavirus was detected in all 50 antigen-positive specimens and 8 of 8 antigen-negative specimens. Nine (75%) of 12 EIA-positive and 1 EIA-negative samples tested culture-positive for vaccine-type rotavirus. Fecal shedding of rotavirus vaccine virus after the first dose of RV5 occurred over a wide range of post-vaccination days not previously studied. These findings will help better define the potential for horizontal transmission of vaccine virus among immunocompromised household contacts of vaccinated infants for future studies"
http://www.ncbi.nlm.nih.gov/pubmed/21477676
" Vaccine-type rotavirus was detected in all 50 antigen-positive specimens and 8 of 8 antigen-negative specimens. Nine (75%) of 12 EIA-positive and 1 EIA-negative samples tested culture-positive for vaccine-type rotavirus. Fecal shedding of rotavirus vaccine virus after the first dose of RV5 occurred over a wide range of post-vaccination days not previously studied."
http://www.ncbi.nlm.nih.gov/pubmed/21477676
These vaccines contain either trace or significant amounts of thimerosal/mercury according to the FDA
- DTaP: Tripedia,
- Flu shots: Fluzone, Fluvirin, Afluria, FluLaval
- DT
- TD
- TT
- Meningococcal: Menomune A, C, AC, and A/C/W-135
INGESTION VS INJECTION
"Intentional subcutaneous or intravenous injection of elemental mercury results in toxicity similar to chronic inorganic mercury exposure, but can also result in severe tissue damage that may require extensive surgical debridement. On the contrary, ingestion of elemental mercury is generally benign and as there is almost no absorption of this form from the GI tract. "
http://www.calpoison.org/hcp/2011/callusvol9no1.htm
Abstract
" Thimerosal generates ethylmercury in aqueous solution and is widely used as preservative. We have investigated the toxicology of Thimerosal in normal human astrocytes, paying particular attention to mitochondrial function and the generation of specific oxidants. We find that ethylmercury not only inhibits mitochondrial respiration leading to a drop in the steady state membrane potential, but also concurrent with these phenomena increases the formation of superoxide, hydrogen peroxide, and Fenton/Haber-Weiss generated hydroxyl radical. These oxidants increase the levels of cellular aldehyde/ketones. Additionally, we find a five-fold increase in the levels of oxidant damaged mitochondrial DNA bases and increases in the levels of mtDNA nicks and blunt-ended breaks. Highly damaged mitochondria are characterized by having very low membrane potentials, increased superoxide/hydrogen peroxide production, and extensively damaged mtDNA and proteins. These mitochondria appear to have undergone a permeability transition, an observation supported by the five-fold increase in Caspase-3 activity observed after Thimerosal treatment." http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395253/
Conclusion: In a dose-response manner, the present study associates an increased organic mercury exposure from Thimerosal-containing hepatitis B vaccines with an increased risk of obesity diagnosis, and suggests that Thimerosal is an obesogen. The results are biologically plausible and future studies are needed to examine this phenomenon.
http://www.ncbi.nlm.nih.gov/pubmed/27583238
"Thimerosal, an organomercurial added as a preservative to some vaccines, is a suspected iatrogenic factor, possibly contributing to paediatric neurodevelopmental disorders including autism. We examined the effects of early postnatal administration of thimerosal (four i.m. injections, 12 or 240 μg THIM-Hg/kg, on postnatal days 7, 9, 11 and 15) on brain pathology in Wistar rats. Numerous neuropathological changes were observed in young adult rats which were treated postnatally with thimerosal. They included: ischaemic degeneration of neurons and "dark" neurons in the prefrontal and temporal cortex, the hippocampus and the cerebellum, pathological changes of the blood vessels in the temporal cortex, diminished synaptophysin reaction in the hippocampus, atrophy of astroglia in the hippocampus and cerebellum, and positive caspase-3 reaction in Bergmann astroglia. These findings document neurotoxic effects of thimerosal, at doses equivalent to those used in infant vaccines or higher, in developing rat brain, suggesting likely involvement of this mercurial in neurodevelopmental disorders." http://www.ncbi.nlm.nih.gov/pubmed/21225508
Maternal transfer of mercury to the developing embryo/fetus: is there a safe level?
“This study focused on standardized embryonic and fetal Hg exposures via primary exposure to the pregnant mother of two common Hg sources (dietary fish and parenteral vaccines). Data demonstrated that Hg exposures, particularly during the first trimester of pregnancy, at well-established dose/weight ratios produced severe damage to humans including death. . In light of research suggestive of a mercuric risk factor for childhood conditions such as tic disorders, cerebral palsy, and autism, it is essential that Hg advisories account for secondary prenatal human exposures.” http://www.tandfonline.com/doi/full/10.1080/02772248.2012.724574
" High blood mercury level was associated with ADHD. Whether the relationship is causal requires further studies.” http://www.ncbi.nlm.nih.gov/pubmed/?term=17177150
" Varicella vaccination is less effective than the natural immunity that existed in prevaccine communities. Universal varicella vaccination has not proven to be cost-effective as increased HZ morbidity has disproportionately offset cost savings associated with reductions in varicella disease. Universal varicella vaccination has failed to provide long-term protection from VZV disease."
http://www.ncbi.nlm.nih.gov/pubmed/22659447
Herpes zoster and meningitis due to reactivation of varicella vaccine virus in an immunocompetent child.
Abstract
Neurologic complications from varicella zoster virus (VZV) reactivation are rare. In this article, we describe a previously immunized child who developed herpes zoster with meningitis. Vaccine strain of VZV was recovered from a skin swab and the cerebrospinal fluid. Reactivation of the vaccine strain of VZV should be recognized as a potential cause of meningitis in children.
https://www.ncbi.nlm.nih.gov/m/pubmed/20844461/
5.4 Risk of Vaccine Virus Transmission
Post-marketing experience suggests that transmission of vaccine virus may occur rarely between healthy vaccinees who develop a varicella-like rash and healthy susceptible contacts. Transmission of vaccine virus from a mother who did not develop a varicella-like rash to her newborn infant has been reported. Due to the concern for transmission of vaccine virus, vaccine recipients should attempt to avoid whenever possible close association with susceptible high-risk individuals for up to six weeks following vaccination with VARIVAX. Susceptible high-risk individuals include:
Immunocompromised Individuals; Pregnant women without documented history of varicella or laboratory evidence of prior infection; Newborn infants of mothers without documented history of varicella or laboratory evidence of prior infection and all newborn infants born at or before 28 weeks gestation regardless of maternal varicella immunity.
http://www.merck.com/product/usa/pi_circulars/v/varivax/varivax_pi.pdf
Varicella Zoster Virus (shingles vaccine) DNA at Inoculation Sites and in Saliva After Zostavax Immunization
Abstract:
"Analysis of 36 individuals over age 60 years who were immunized with Zostavax revealed varicella zoster virus (VZV) DNA in swabs of skin inoculation sites obtained immediately after immunization in 18 (50%) of 36 subjects (copy number per nanogram of total DNA, 28 to 2.1 × 10 6 ) and in saliva collected over 28 days in 21 (58%) of 36 subjects (copy number, 20 to 248). Genotypic analysis of DNA extracted from 9 random saliva samples identified vaccine virus in all instances. In some immunized individuals over age 60, vaccine virus DNA is shed in saliva up to 4 weeks."
Results:
" No saliva specimen collected immediately before immunization contained VZV DNA. During the first week after immunization, VZV DNA was detected in saliva of 21 (58%) of 36 subjects (13 men and 8 women). During the 28-day study period, VZV DNA was found in 11 (31%) of 36 subjects (5 men and 6 women) at day 14, in 10 (28%) of 36 subjects (6 men and 4 women) at day 21, and in 2 (6%) of 36 subjects (1 man and 1 woman) at day 28. Figure 1 shows the percent of immunized subjects who shed VZV DNA during the 28-day study period. VZV DNA copy numbers per nanogram of total DNA ranged from 20 to 248 (Table 1). Genotypic analysis of DNA from 9 random saliva samples revealed vaccine virus DNA in all instances (Table 1, bold); wild-type VZV DNA was not detected. In 15 (42%) of 36 vaccine recipients (6 men, 9 women), VZV DNA was not detected in saliva at any time during the 28-day study period."
http://jid.oxfordjournals.org/content/203/11/1542.long
" Pertussis can still be found in a fifth of school age children who present in primary care with persistent cough and can cause clinically significant cough in fully vaccinated children." http://www.ncbi.nlm.nih.gov/pubmed/24961836
Unvaccinated children do not significantly contribute to whooping cough outbreaks
Cdc statistics show there are more cases of whooping cough (pertussis) in vaccinated/up to date on vaccine individuals. See links and following images.
https://www.cdc.gov/pertussis/downloads/pertuss-surv-report-2012.pdf
https://www.cdc.gov/pertussis/downloads/pertussis-surveillance-report.pdf
https://www.cdc.gov/pertussis/downloads/pertuss-surv-report-2014.pdf
https://www.cdc.gov/pertussis/downloads/pertuss-surv-report-2015.pdf
" Our unvaccinated and under vaccinated population did not appear to contribute significantly to the increased rate of clinical pertussis. Surprisingly, the highest incidence of disease was among previously vaccinated children aged 8–12 years. We sought to examine the factors that resulted in this peak."
"Of the 132 individuals (77.2%) aged ≤18 years at time of illness, 81% were fully vaccinated, 11% were undervaccinated, and 8% were never vaccinated. Of the 103 individuals (60.2%) aged ≤12 years, 85% were fully vaccinated, 7% were undervaccinated, and 8% were never vaccinated."
http://cid.oxfordjournals.org/content/54/12/1730.full
Effectiveness of pertussis vaccines for adolescents and adults: case-control study
"The adjusted estimate of effectiveness of Tdap vaccination against pertussis was 53.0."
http://www.bmj.com/content/347/bmj.f4249
"vaccination led to a 40-fold enhancement of B. parapertussis colonization in the lungs of mice.. these data suggest that the vaccine may be contributing to the observed rise in whooping cough incidence over the last decade by promoting B. parapertussis infection.”
Conclusions
"In low-income countries with high mortality, DTP as the last vaccine received may be associated with slightly increased mortality. Since the pattern was inversed for BCG, the effect is unlikely to be due to higher-risk children having received vaccination. The role of DTP in high mortality areas needs to be clarified."
http://www.ncbi.nlm.nih.gov/pubmed/15082643
The odds of having a history of asthma was twice as great among vaccinated subjects than among unvaccinated subjects (adjusted odds ratio, 2.00; 95% confidence interval, 0.59 to 6.74). The odds of having had any allergy-related respiratory symptom in the past 12 months was 63% greater among vaccinated subjects than unvaccinated subjects (adjusted odds ratio, 1.63; 95% confidence interval, 1.05 to 2.54). The associations between vaccination and subsequent allergies and symptoms were greatest among children aged 5 through 10 years.
DTP or tetanus vaccination appears to increase the risk of allergies and related respiratory symptoms in children and adolescents. Although it is unlikely that these results are entirely because of any sources of bias, the small number of unvaccinated subjects and the study design limit our ability to make firm causal inferences about the true magnitude of effect.
http://www.ncbi.nlm.nih.gov/pubmed/10714532
Adverse events following Haemophilus influenzae type b vaccines in the Vaccine Adverse Event Reporting System, 1990-2013
RESULTS:
VAERS received 29,747 reports after Hib vaccines; 5179 (17%) were serious, including 896 reports of deaths. Median age was 6 months (range 0-1022 months). Sudden infant death syndrome was the stated cause of death in 384 (51%) of 749 death reports with autopsy/death certificate records. The most common nondeath serious AE categories were neurologic (80; 37%), other noninfectious (46; 22%) (comprising mainly constitutional signs and symptoms); and gastrointestinal (39; 18%) conditions.
https://www.ncbi.nlm.nih.gov/pubmed/25598306
*********** AUTISM *********
Methodological Issues and Evidence of Malfeasance in Research Purporting to Show Thimerosal in Vaccines Is Safe
Conclusion
As seen in this review, the studies upon which the CDC relies and over which it exerted some level of control report that there is no increased risk of autism from exposure to organic Hg in vaccines, and some of these studies even reported that exposure to Thimerosal appeared to decrease the risk of autism. These six studies are in sharp contrast to research conducted by independent researchers over the past 75+ years that have consistently found Thimerosal to be harmful. As mentioned in the Introduction section, many studies conducted by independent investigators have found Thimerosal to be associated with neurodevelopmental disorders. Several studies, for example, including three of the six studies covered in this review, have found Thimerosal to be a risk factor for tics [10, 17, 24, 25, 34, 35]. In addition, Thimerosal has been found to be a risk factor in speech delay, language delay, attention deficit disorder, and autism [10, 11, 15–17, 24, 25, 34].
Considering that there are many studies conducted by independent researchers which show a relationship between Thimerosal and neurodevelopmental disorders, the results of the six studies examined in this review, particularly those showing the protective effects of Thimerosal, should bring into question the validity of the methodology used in the studies. A list of the most common methodological issues with these six studies is shown in Table 1. Importantly, other than the Hviid et al. [23] study, five of the publications examined in this review were directly commissioned by the CDC, raising the possible issue of conflict of interests or research bias, since vaccine promotion is a central mission of the CDC. Conceivably, if serious neurological disorders are found to be related to Thimerosal in vaccines, such findings could possibly be viewed as damaging to the vaccine program.
"Boys vaccinated as neonates had threefold greater odds for autism diagnosis compared to boys never vaccinated or vaccinated after the first month of life. Non-Hispanic white boys were 64% less likely to have autism diagnosis relative to nonwhite boys. Findings suggest that U.S. male neonates vaccinated with the hepatitis B vaccine prior to 1999 (from vaccination record) had a threefold higher risk for parental report of autism diagnosis compared to boys not vaccinated as neonates during that same time period. Nonwhite boys bore a greater risk."
http://www.ncbi.nlm.nih.gov/m/pubmed/21058170/
Conclusions
The present study provides new epidemiologic evidence showing that African American males receiving the MMR vaccine prior to 24 months of age or 36 months of age are more likely to receive an autism diagnosis.
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders.
"the potential effects of conjugate vaccines on neural development merit close examination. Conjugate vaccines fundamentally change the manner in which the immune systems of infants and young children function by deviating their immune responses to the targeted carbohydrate antigens from a state of hypo-responsiveness to a robust B2 B cell mediated response. This period of hypo-responsiveness to carbohydrate antigens coincides with the intense myelination process in infants and young children, and conjugate vaccines may have disrupted evolutionary forces that favored early brain development over the need to protect infants and young children from capsular bacteria."
http://www.ncbi.nlm.nih.gov/pubmed/21993250
Serological association of measles virus and human herpesvirus-6 with brain autoantibodies in autism.
"Considering an autoimmunity and autism connection, brain autoantibodies to myelin basic protein (anti-MBP) and neuron-axon filament protein (anti-NAFP) have been found in autistic children. In this current study, we examined associations between virus serology and autoantibody by simultaneous analysis of measles virus antibody (measles-IgG), human herpesvirus-6 antibody (HHV-6-IgG), anti-MBP, and anti-NAFP. We found that measles-IgG and HHV-6-IgG titers were moderately higher in autistic children but they did not significantly differ from normal controls. Moreover, we found that a vast majority of virus serology-positive autistic sera was also positive for brain autoantibody: (i) 90% of measles-IgG-positive autistic sera was also positive for anti-MBP; (ii) 73% of measles-IgG-positive autistic sera was also positive for anti-NAFP; (iii) 84% of HHV-6-IgG-positive autistic sera was also positive for anti-MBP; and (iv) 72% of HHV-6-IgG-positive autistic sera was also positive for anti-NAFP. This study is the first to report an association between virus serology and brain autoantibody in autism; it supports the hypothesis that a virus-induced autoimmune response may play a causal role in autism."
http://www.ncbi.nlm.nih.gov/pubmed/9756729
Abstract
"There is a compelling argument that the occurrence of regressive autism is attributable to genetic and chromosomal abnormalities, arising from the overuse of vaccines, which subsequently affects the stability and function of the autonomic nervous system and physiological systems. That sense perception is linked to the autonomic nervous system and the function of the physiological systems enables us to examine the significance of autistic symptoms from a systemic perspective. Failure of the excretory system influences elimination of heavy metals and facilitates their accumulation and subsequent manifestation as neurotoxins: the long-term consequences of which would lead to neurodegeneration, cognitive and developmental problems. It may also influence regulation of neural hyperthermia. This article explores the issues and concludes that sensory dysfunction and systemic failure, manifested as autism, is the inevitable consequence arising from subtle DNA alteration and consequently from the overuse of vaccines."
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/
Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure
“Autism is a condition characterized by impaired cognitive and social skills, associated with compromised immune function. The incidence is alarmingly on the rise, and environmental factors are increasingly suspected to play a role. This paper investigates word frequency patterns in the U.S. CDC Vaccine Adverse Events Reporting System (VAERS) database. Our results provide strong evidence supporting a link between autism and the aluminum in vaccines. A literature review showing toxicity of aluminum in human physiology offers further support. Mentions of autism in VAERS increased steadily at the end of the last century, during a period when mercury was being phased out, while aluminum adjuvant burden was being increased. Using standard log-likelihood ratio techniques, we identify several signs and symptoms that are significantly more prevalent in vaccine reports after 2000, including cellulitis, seizure, depression, fatigue, pain and death, which are also significantly associated with aluminum-containing vaccines. We propose that children with the autism diagnosis are especially vulnerable to toxic metals such as aluminum and mercury due to insufficient serum sulfate and glutathione. A strong correlation between autism and the MMR (Measles, Mumps, Rubella) vaccine is also observed, which may be partially explained via an increased sensitivity to acetaminophen administered to control fever.”
http://www.mdpi.com/1099-4300/14/11/2227
full text: http://groups.csail.mit.edu/sls/publications/2012/entropy-14-02227.pdf
"Acetaminophen use after measles-mumps-rubella vaccination was SIGNIFICANTLY associated with autistic disorder when considering children 5 years of age or less, after limiting cases to children with regression in development and when considering only children who had post-vaccination sequelae adjusting for age, gender, mother’s ethnicity, and the presence of illness concurrent with measles-mumps-rubella vaccination. Ibuprofen use after measles-mumps-rubella vaccination was not associated with autistic disorder. This preliminary study found that acetaminophen use after measles-mumps-rubella vaccination was associated with autistic disorder."
http://www.ncbi.nlm.nih.gov/pubmed/18445737
Neurologic Adverse Events Following Vaccination (Progress in Health Sciences Vol. 2(1) 2012•pp 129-141.)
“Conclusions: Despite the assurances of the necessity and safety of vaccinations, there are more and more questions and doubts, which both physicians and parents are waiting to be clarified… It seems that it would be worthwhile to apply the precautionary principle – the ethical principle (from 1988) according to which if there is a probable, although poorly known, risk of adverse effects of new technology, it is better not to implement it rather than risk uncertain but potentially very harmful consequences.”
http://progress.umb.edu.pl/sites/progress.umb.edu.pl/files/129-141.pdf
Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism.
“Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.”
http://www.ncbi.nlm.nih.gov/pubmed/12145534
"A 1% increase in vaccination was associated with an additional 680 children having AUT or SLI. Neither parental behavior nor access to care affected the results, since vaccination proportions were not significantly related (statistically) to any other disability or to the number of pediatricians in a U.S. state. The results suggest that although mercury has been removed from many vaccines, other culprits may link vaccines to autism. Further study into the relationship between vaccines and autism is warranted”
http://www.ncbi.nlm.nih.gov/pubmed/21623535
“Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies. Using serum samples of 125 autistic children and 92 control children, antibodies were assayed by ELISA or immunoblotting methods. ELISA analysis showed a significant increase in the level of MMR antibodies in autistic children. Immunoblotting analysis revealed the presence of an unusual MMR antibody in 75 of 125 (60%) autistic sera but not in control sera. This antibody specifically detected a protein of 73-75 kD of MMR. This protein band, as analyzed with monoclonal anti bodies, was immunopositive for measles hemagglutinin (HA) protein but not for measles nucleoprotein and rubella or mumps viral proteins. Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.”
http://www.ncbi.nlm.nih.gov/pubmed/12145534
124 medical research on vaccine and autism
http://www.scribd.com/mobile/doc/220807175
“Virus-induced autoimmunity may play a causal role in autism. To examine the etiologic link of viruses in this brain disorder, we conducted a serologic study of measles virus, mumps virus, and rubella virus. Viral antibodies were measured by enzyme-linked immunosorbent assay in the serum of autistic children, normal children, and siblings of autistic children. The level of measles antibody, but not mumps or rubella antibodies, was significantly higher in autistic children as compared with normal children (P = 0.003) or siblings of autistic children (P <or= 0. 0001). Furthermore, immunoblotting of measles vaccine virus revealed that the antibody was directed against a protein of approximately 74 kd molecular weight. The antibody to this antigen was found in 83% of autistic children but not in normal children or siblings of autistic children. Thus autistic children have a hyperimmune response to measles virus, which in the absence of a wild type of measles infection might be a sign of an abnormal immune reaction to the vaccine strain or virus reactivation.” http://www.ncbi.nlm.nih.gov/pubmed/12849883
Adverse Drug Reactions of Spontaneous Reports in Shanghai Pediatric Population
Results:
"A male overrepresentation was observed regarding the total number of reports. The most frequently reported group of drugs were vaccines (42.15%). Skin rash and fever were the commonest symptoms reported in the total pediatric dataset. The proportion of children that suffered from a serious ADR was 2.16% and that for drug related deaths was 0.34%. And we found that the multiple drug exposure experienced a high proportion of serious ADRs compared with the single drug use (χ = 15.99, P<0.0001). Sixty-five percent of ADRs were for children less than 6 years of age. And more than half of reports were from doctors."
" The 3848 reports included 4430 suspected ADRs, with an average of over 10 reports per day and 1.15 ADRs per child. There were 666 reports, which cited more than one suspected drug. The total number of suspected drugs in pediatric reports was 4619 with a mean number of 1.20 drugs per child."
ADRs by Vaccines and Non-vaccines:
"The single most common reaction was exanthema, followed by fever, application site reaction and vomiting. Regarding assessment of drugs, the most frequent reports were related to vaccine use (1622 reports, 42.15%). When the non-vaccine related reports were discriminated by excluding children that had been reported to have a suspected ADR of a vaccination, the total number of children, whom an ADR had been related to, were then reduced to 2649. Skin reactions were still most frequently reported. The most commonly reported drugs among serious reports were antibacterials for systemic use (32.82%), nervous system (17.56%) and vaccines (13.74%)."
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933652
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Poul Thorsen, the man that conducted the study for the CDC claiming there is no link between vaccines and autism, is on the most wanted fugitive list for the Office of Inspector General for stealing over $1 million in grant money from the CDC. Thorsen submitted fraudulent invoices on CDC letterhead to medical facilities assisting in the research for reimbursement of work allegedly covered by the grants. The invoices were addressed to Aarhaus University and Sahlgrenska University Hospital. The fact that the invoices were on CDC letterhead made it appear that CDC was requesting the money from Aarhaus University and Sahlgrenska University Hospital although the bank account listed on the invoices belonged to Thorsen.
https://oig.hhs.gov/fraud/fugitives/profiles.asp#thorsen
"Thorsen's 2003 Danish study reported a 20-fold increase in autism in Denmark after that country banned mercury based preservatives in its vaccines. His study concluded that mercury could therefore not be the culprit behind the autism epidemic.
His study has long been criticized as fraudulent since it failed to disclose that the increase was an artifact of new mandates requiring, for the first time, that autism cases be reported on the national registry. This new law and the opening of a clinic dedicated to autism treatment in Copenhagen accounted for the sudden rise in reported cases rather than, as Thorsen seemed to suggest, the removal of mercury from vaccines."
http://www.huffingtonpost.com/robert-f-kennedy-jr/central-figure-in-cdc-vac_b_494303.html
Thorsen's partner Kreesten Madsen recently came under fierce criticism after damning e-mails surfaced showing Madsen in cahoots with CDC officials intent on fraudulently cherry picking facts to prove vaccine safety.
http://www.putchildrenfirst.org/chapter5.html
"Rising autistic disorder prevalence is directly related to vaccines manufactured utilizing human fetal cells."
http://www.ms.academicjournals.org/article/article1409245960_Deisher%20et%20al.pdf
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According to two Merck scientists who filed a False Claims Act complaint in 2010 vaccine manufacturer Merck knowingly falsified its mumps vaccine test data, spiked blood samples with animal antibodies, sold a vaccine that actually promoted mumps and measles outbreaks, and ripped off governments and consumers who bought the vaccine thinking it was "95% effective."
http://www.courthousenews.com/2012/06/27/47851.htm
GlaxoSmithKline (GSK) also produces vaccines
A roughly nine-year federal investigation has exposed GSK's rampant abuse of the law by illegally marketing drugs, forging drug safety data, bribing doctors to promote dangerous and expensive drugs, ripping off Medicare and Medicaid, and lying about the effectiveness and safety of drugs
CDC labs close due to cross contamination of anthrax, small pox, and deadly flu strain
http://www.cidrap.umn.edu/news-perspective/2014/07/more-problems-shutter-cdc-labs-prompt-review
CDC says it improperly sent deadly pathogens at least 5 times in the past decade
CDC caught transporting anthrax in zip lock sandwhich bags
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Doctors that question the safety of vaccines:
1. Dr. Nancy Banks - http://bit.ly/1Ip0aIm
2. Dr. Russell Blaylock - http://bit.ly/1BXxQZL
3. Dr. Shiv Chopra - http://bit.ly/1gdgh1s
4. Dr. Sherri Tenpenny - http://bit.ly/1MPVbjx
5. Dr. Suzanne Humphries - http://bit.ly/17sKDbf
6. Dr. Larry Palevsky - http://bit.ly/1LLEjf6
7. Dr. Toni Bark - http://bit.ly/1CYM9RB
8. Dr. Andrew Wakefield - http://bit.ly/1MuyNzo
9. Dr. Meryl Nass - http://bit.ly/1DGzJsc
10. Dr. Raymond Obomsawin - http://bit.ly/1G9ZXYl
11. Dr. Ghislaine Lanctot - http://bit.ly/1MrVeUL
12. Dr. Robert Rowen - http://bit.ly/1SIELeF
13. Dr. David Ayoub - http://bit.ly/1SIELve
14. Dr. Boyd Haley PhD - http://bit.ly/1KsdVby
15. Dr. Rashid Buttar - http://bit.ly/1gWOkL6
16. Dr. Roby Mitchell - http://bit.ly/1gdgEZU
17. Dr. Ken Stoller - http://bit.ly/1MPVqLI
18. Dr. Mayer Eisenstein - http://bit.ly/1LLEqHH
19. Dr. Frank Engley, PhD - http://bit.ly/1OHbLDI
20. Dr. David Davis - http://bit.ly/1gdgJwo
21. Dr Tetyana Obukhanych - http://bit.ly/16Z7k6J
22. Dr. Harold E Buttram - http://bit.ly/1Kru6Df
23. Dr. Kelly Brogan - http://bit.ly/1D31pfQ
24. Dr. RC Tent - http://bit.ly/1MPVwmu
25. Dr. Rebecca Carley - http://bit.ly/K49F4d
26. Dr. Andrew Moulden - http://bit.ly/1fwzKJu
27. Dr. Jack Wolfson - http://bit.ly/1wtPHRA
28. Dr. Michael Elice - http://bit.ly/1KsdpKA
29. Dr. Terry Wahls - http://bit.ly/1gWOBhd
30. Dr. Stephanie Seneff - http://bit.ly/1OtWxAY
31. Dr. Paul Thomas - http://bit.ly/1DpeXPf
32. Many doctors talking at once - http://bit.ly/1MPVHOv
33. Dr. Richard Moskowitz - http://bit.ly/1OtWG7D
34. Dr. Jane Orient - http://bit.ly/1MXX7pb
35. Dr. Richard Deth - http://bit.ly/1GQDL10
36. Dr. Lucija Tomljenovic - http://bit.ly/1eqiPr5
37. Dr Chris Shaw - http://bit.ly/1IlGiBp
38. Dr. Susan McCreadie - http://bit.ly/1CqqN83
39. Dr. Mary Ann Block - http://bit.ly/1OHcyUX
40. Dr. David Brownstein - http://bit.ly/1EaHl9A
41. Dr. Jayne Donegan - http://bit.ly/1wOk4Zz
42. Dr. Troy Ross - http://bit.ly/1IlGlNH
43. Dr. Philip Incao - http://bit.ly/1ghE7sS
44. Dr. Joseph Mercola - http://bit.ly/18dE38I
45. Dr. Jeff Bradstreet - http://bit.ly/1MaX0cC
46. Dr. Robert Mendelson - http://bit.ly/1JpAEQr
47. Dr. Garth Nicolson - http://bit.ly/1OQVJsF
48. Dr. Marc Girard - http://bit.ly/1iw0smT
49. Dr. Charles Richet - http://bit.ly/1G5GG7j
50. Dr. Zac Bush - http://bit.ly/1LS19OZ
Vaccine inserts:
http://www.vaccinesafety.edu/package_inserts.htm
VAERS reporting:
https://vaers.hhs.gov/esub/index
Compensation table:
http://www.hrsa.gov/vaccinecompensation/vaccinetable.html
How Vaccinations Affect the Developing Immune System
The purpose of vaccinations is to introduce a pathogen (i.e. virus, bacteria, etc.) to the immune system so that a person can develop immunity to the pathogen without having to experience disease.
So how do vaccines work if they do not cause the disease they are intended to protect against? A killed, inactivated or portion of a pathogen (virus, bacteria, etc.) is injected into the body to get the immune system to recognize it, but since the pathogen is inactivated, it should not cause the disease.
So obviously the reaction of the immune system is different to a vaccine than if it were to encounter the natural pathogen in the environment. First of all, the mode of entry of the pathogen is different. In normal circumstances, most pathogens enter a person through the nose or mouth. In most vaccinations, the pathogen enters through an injection, completely bypassing the normals lines of the immune system’s defense.
This would not be a major problem if the injection contained simply a killed or inactivated pathogen, as this would not pose a threat. However, since the pathogens are not a threat to cause an immune system reaction, vaccines contain something called an adjuvant, which is placed in a vaccine to cause a strong immune response.
Most vaccines use aluminum as an adjuvant, which is a neurotoxin that triggers the necessary heightened immune system response. With the immune system in an alarmed state, it then reacts to everything in the vaccine (see “Vaccine Ingredients”), including the inactivated pathogen.
It is a brilliant strategy, as it allows vaccines to manipulate the immune system to develop antibodies to the specific pathogen, without progressing to the symptoms of the actual disease. However, as we learn more about the immune system, we learn there is much more to an immune response than the production of antibodies.
And with that increased knowledge, we are learning that there are consequences that go along with attempting to trick the immune system through introducing a pathogen under false pretenses.
In the late 1980’s cells of the immune system that help regulate immunity called helper T cells, particularly Th1 and Th2, were discovered that helped give a better understanding of immune system function.
Th1 cells help regulate cell-mediated immunity (CMI) which help deal with pathogens that present a threat to get within cells. Viruses for example, which cannot replicate on their own, can only establish an infection by getting inside of a host’s cell and uses the cell’s reproductive machinery to replicate. The cell then bursts open, producing multitudes of newly made viruses.
One of the tools of CMI is the cytotoxic lymphocyte (CTL) also known as the Killer T Cell, which destroys virus infected cells.
Th2 cells help regulate humoral immunity which help deal with pathogens that present a threat outside of cells. One of the main weapons of the Th2 response are antibodies, which can attach to specific invaders and help to be more easily identified by other cells of the immune system such as macrophages and aid in their elimination.
The production antibodies are present in both the Th1 and Th2 responses, as they can also attach to pathogens such as viruses and prevent their entry into cells. However, the antibody response is substantially higher with a Th2 response as there is no threat of the pathogen getting into the cell.
Therefore the normal response of the immune system to pathogens such as viruses would be a Th1 response where there would be antibodies produced to prevent viruses from getting inside of cells, and also a significant amount of killer T cells (CTL) to destroy virus infected cells.
The normal response to pathogens that offer no threat to get inside of cells would be a Th2 response, in which there would be a high antibody response to most efficiently deal with the pathogen.
So what type of helper T cell response do vaccines elicit? First of all, the criteria that researchers look at to determine vaccine response is the level of antibody titers that are found following vaccination. In other words, the higher the antibody response, the more effective the vaccine is deemed to be. What helper T cell elicits the highest antibody response? Th2.
This subject was addressed in a 1995 paper titled “Vaccine strategies: targeting helper T cell responses.” The paper considers the need to elicit the appropriate helper T cell response through vaccination.
- “Vaccine strategies need to take into account the balance of T helper subsets they induce. Th1 cells…are associated with CMI rather than humoral responses, and afford protection against intracellular infections including parasites.”
- “Th2 cells… elicit high-titer antibody responses and poor CMI and are associated with susceptibility with intracellular pathogens.”
- “Once the type of Th cell response that is protective is identified, it may be possible to combine a protein with an adjuvant or link it to a carrier that will promote responses towards the most advantageous Th subset.”
- Although it does not specifically state what type of response is being elicited, the last quote indicates it is not the most advantageous response.
Vaccine strategies: targeting helper T cell responses. Golding B; Scott DE; Ann NY Acad Sci, 754(-VI-):126-37 1995 May 31- http://www.ncbi.nlm.nih.gov/pubmed/7625646
The fact that vaccines still elicit an improper immune response today is confirmed in this article below admitting not only that vaccines produce an incorrect immune response, but also that the vaccines we use today were developed with a poor understanding of how the immune system works in the first place.
- “Although vaccination has been used for centuries, the technologies are largely empirical with little understanding of the underlying immunological principles and physiological mechanisms.”
- “As researchers gain knowledge of these principles and regulatory authorities become more stringent in their requirements, changes in empirical approaches have become necessary; rational vaccine design is now essential.”
- “The articles in this special feature introduce research on a new generation of vaccines which are logically designed and evaluated. Of particular interest is a new wave of vaccines that induce CD8+ T cell responses — in contrast to the traditional mechanism of eliciting a protective antibody response — and how they may be used therapeutically.”
The Journal of Immunology and Cell Biology, May/June 2009, Volume 87, No. 4, July 2009, Volume 87, No. 5 - http://www.nature.com/icb/focus/vaccine_web_focus/index.html
So again, what type of helper T cell subsets do vaccines elicit? This question was also addressed in a Health Research of Allied Forces Project that examines the relationship between immunological markers of Th1/Th2 cytokine balance, biological warfare and Gulf War related illness.
“Amongst Gulf War veterans, there was a significant trend for reduced levels of the Th1 cytokine IFN-g and non-significant trends for increased levels of the Th2 cytokines IL-4 and IL-10 with increasing numbers of vaccines administered.”
“Multiple vaccine exposure was associated with evidence of Th1/Th2 imbalance in favor of Th2, but since vaccine exposure in the symptomatic and well Gulf war veterans we studied was similar, we are unable to confirm a causative link between vaccines, Th1/Th2 balance, and illness.”
So what the project found was vaccines increased levels of Th2 and decreased levels of Th1. They could not confirm that the imbalance of Th1/Th2 was linked to illness, which means that although they found these imbalances, not everyone presented signs of illness.
So what are the consequences of having a Th1/Th2 imbalance in favor of Th2? The Health Research of Allied Forces Project found “An imbalance of Th2 over Th1 immunity is associated with allergic disease and hypersensitivity and mood changes including depression.”
http://www.gulflink.osd.mil/medsearch/HealthResearchOfAlliedFo/DoD106.shtml
In a paper from The Journal of Clinical Investigation it was noted “Allergic asthma, which is present in as many as 10% of individuals in industrialized nations, is characterized by chronic airway inflammation and hyperreactivity induced by allergen-specific Th2 cells secreting interleuken-4 (IL-4) and IL-5… Because Th1 cells antagonize Th2 cell functions, it has been proposed that immune deviation toward Th1 can protect against asthma and allergies.”
However, they found that when they attempted to artificially counterbalance Th2 cell-induced airway hyperactivity with allergen specific Th1 cells, it actually caused severe airway inflammation. This finding would suggest that there is much more to Th1/Th2 helper T-cell function and balance through natural infection than we understand at this time.
J Clin Invest, January 1999, Volume 103, Number 2, 175-183 - http://www.jci.org/articles/view/5155/version/1
So in addition to how a Th1 response offers protection to pathogens that pose a threat to get inside of cells and a Th2 response offers protection against pathogens outside of cells, what else do we understand about Th1/Th2 function and balance?
First of all, even though it is understood that a healthy adult has a balanced Th1/Th2 cytokine profile, we do not start out that way. In a healthy baby at birth the Th1/Th2 profile is actually heavily shifted towards Th2.
To understand why this is the case, we must first look at the primary purpose of the immune system – identifying self from non-self. It is this characteristic of the immune system that make each person unique not only from their environment but also from every other person on earth.
One of the immune system cells discussed earlier plays an important role in this function of the immune system – the cytotoxic lymphocyte (CTL) or Killer T cell. In addition to identifying and destroying virus infected cells, Killer T cells also destroy cells that are non-self.
For example, in the case of an organ transplant, the reason an organ is rejected is because it is detected by the immune system as non-self and destroyed by the Killer T cells. That is why it is important to match organ donor with the recipient as closely as possible in addition to suppressing the immune system of the recipient in order for the transplant to be successful.
So what does this have to do with a baby being born with his or her immune system shifted heavily towards Th2? Well, where does baby come from? Mother. Is baby the same person as mom? Of course not. Therefore the mother must somehow allow someone who is non-self (baby) to develop and grow without her own immune system destroying her own child.
Obviously this is allowed to happen, but how? The answer is another amazing and brilliant design in our creation. The placenta, which provides nourishment for the baby, also secretes chemicals (primarily progesterone) which shifts mom’s Th1/Th2 chemical profile away from Th1 and towards Th2.
Why does mom’s immune system need to be shifted away from Th1? It is the Th1 Helper T cells that promote the production of Killer T cells which would destroy cells that are non-self, in this case, the baby.
Therefore the baby develops in a Th2 rich environment and born with his or her chemical profile shifted towards Th2.
So if a normal healthy adult has a balanced Th1/Th2 profile, how does a baby then go on to increase his or her Th1 to achieve this balance? Well, what triggers a Th1 response? An encounter with microbes in the environment that could potential offer a threat of infection by getting inside of cells, such as viruses and bacteria.
Multiple exposures throughout childhood which trigger a Th1 response help to build this Th1 chemical profile to develop the child’s immune system.
What is one sign that a child is dealing with a viral or bacterial infection? A fever. In a study funded by the National Institute of Allergy and Infectious Diseases (NIAID), part of the NIH, found that infants who experience fevers before their first birthday are less likely to develop allergies by ages six or seven.
http://www.sciencedaily.com/releases/2004/02/040210080041.htm
What does this tell us? These fevers are commonly a sign of a Th1 response, and from the NIAID study, with increased fevers (increased Th1) children were less likely to develop allergies.
We find further evidence of this when we look specifically at the measles virus. In 2009, a large study in Europe published in Pediatrics found that children who’ve been infected with measles are less likely to develop allergies.
Among the children who never had a measles infection, those who had been vaccinated were more likely to have nasal allergies. Allergies were less likely in children who had had a bout of measles, but not in those who had been vaccinated against the measles
http://www.reuters.com/article/healthNews/idUSTRE5236HS20090304
How then do vaccines work if they do not provide the proper immune response? Let’s use the measles for example. When a child is vaccinated for the measles, instead of having the normal Th1 response for a virus, the child will have a Th2 response due to the vaccine.
Now one of the goals of vaccinating is to create a memory in the immune system so that when a child comes across the measles virus in the environment his immune system has already been trained to have a quick response. Since the immune system has been trained to have a Th2 response, that is the response it will have to the wild measles virus, instead of the normal Th1 response.
This Th2 response will elicit high antibody production. These antibodies will attach to the measles virus which will aid macrophages in identifying them and also will prevent entry into cells. However any viruses that get past the antibody defense and into cells will be able to replicate due to the lack of Killer T cells that would normally be present in the Th1 response.
These newly made viruses will burst out of the high-jacked cells. Since there are a high level of antibodies to these measles viruses, they will again attached to these viruses, tagging them for destruction and preventing them from getting into cells. However, any of these new viruses that get past the antibody defense and into the cells can also replicate and repeat the process over again.
So what we end up with is a chronic measles infection that never actually shows up as the measles. The vaccine has prevented the disease, but at what price?
In 1998 Dr. Andrew Wakefield observed a possible connection between inflammatory bowel disorder (chronic enterocolitis), regressive developmental disorder, and the MMR vaccine.
http://www.ncbi.nlm.nih.gov/pubmed/9500320
In 2001 John O'Leary, Professor of Pathology at St James's Hospital and Trinity College, Dublin, replicated his findings.
Now a team from the Wake Forest University School of Medicine in North Carolina are examining 275 children with regressive autism and bowel disease - and of the 82 tested so far, 70 prove positive for the measles virus.
http://www.dailymail.co.uk/news/article-388051/Scientists-fear-MMR-link-autism.html
Summary
So what does this really mean? Many vaccines may be effective in preventing disease, but since vaccines cause an abnormal immune system response, it hinders the development of the immune system, resulting in inappropriate responses to normal environmental stimuli.
Influence of pediatric vaccines on amygdala growth and opioid ligand binding in rhesus macaque infants: A pilot study
"This longitudinal, case-control pilot study examined amygdala growth in rhesus macaque infants receiving the complete US childhood vaccine schedule (1994-1999). Longitudinal structural and functional neuroimaging was undertaken to examine central effects of the vaccine regimen on the developing brain. Vaccine-exposed and saline-injected control infants underwent MRI and PET imaging at approximately 4 and 6 months of age, representing two specific timeframes within the vaccination schedule. Volumetric analyses showed that exposed animals did not undergo the maturational changes over time in amygdala volume that was observed in unexposed animals. After controlling for left amygdala volume, the binding of the opioid antagonist [11C]diprenorphine (DPN) in exposed animals remained relatively constant over time, compared with unexposed animals, in which a significant decrease in [11C]DPN binding occurred. These results suggest that maturational changes in amygdala volume and the binding capacity of [11C]DPN in the amygdala was significantly altered in infant macaques receiving the vaccine schedule. The macaque infant is a relevant animal model in which to investigate specific environmental exposures and structural/functional neuroimaging during neurodevelopment."
CONCLUSIONS
In this pilot study, infant macaques receiving the recommended pediatric vaccine regimen from the 1990’s displayed a different pattern of maturational changes in amygdala volume and differences in amygdala-binding of [11C]DPN following the MMR/DTaP/Hib vaccinations between T1 and T2 compared with non-exposed animals. There was also evidence of greater total brain volume in the exposed group prior to these vaccinations suggesting a possible effect of previous vaccinations to which these animals had been exposed. Because primate testing is an important aspect of pre-clinical vaccine safety assessment prior to approval for human use (Kennedy et al. 1997), the results of this pilot study warrant additional research into the potential impact of an interaction between the MMR and thimerosal-containing vaccines on brain structure and function. Additional studies are underway in the primate model to investigate the mechanistic basis for this apparent interaction.
SOURCE: http://www.ane.pl/pdf/7020.pdf
Amygdala
The amygdala (Latin, corpus amygdaloideum) is an almond-shape set of neurons located deep in the brain's medial temporal lobe.
Shown to play a key role in the processsing of emotions, the amygdala forms part of the limbic system.
In humans and other animals, this subcortical brain structure is linked to both fear responses and pleasure.
Its size is positively correlated with aggressive behavior across species.
In humans, it is the most sexually-dimorphic brain structure, and shrinks by more than 30% in males upon castration.
Conditions such as anxiety, autism, depression, post-traumatic stress disorder, and phobias are suspected of being linked to abnormal functioning of the amygdala, owing to damage, developmental problems, or neurotransmitter imbalance.
https://www.sciencedaily.com/terms/amygdala.htm
Memo put out by Wyeth Pharmaceuticals discussing a decision to not put out more than a certain amount of vials from vaccine lots in one area after there were a cluster of SIDS deaths caused by the DPT and DPTH vaccines in Tennessee.
Download it in pdf form here: https://goo.gl/61bvAl
