Vax Poisons

The Certifiably Lethal Concoctions in Vaccines

Below we have begun a partial list of some of the toxic swill of admitted excipients that mostly are for no justifiable reason other than for eugenic herd-thinning purposes and/or sickening the masses for subsequent medical profit dumped into vaccines

Following the list is a link to the CDC website page which mindlessly dares to provide a list of vaccines and their known excipients. After you have perused the following list of vaccine poisons and their adverse effects like seizures, paralysis and death take a look at the CDCs vaccines, their admittedly poisonous ingredients, and ask yourself why you should blindly allow you and yours to have these shamelessly poisonous concoctions routinely injected directly into your bodies, which accumulate in body tissue, organs, bones and the brain, and interact synergistically

  • Aluminum is a neurotoxin which induces neuron death. It is even more toxic when synergistically combined with mercury. It plays a role in neurodegenerative diseases (Alzheimer’s, Autism, Parkinson’s, etc.), autoimmunity, blood diseases, bone diseases, and many other serious health disorders.

  • Ammonium Sulfate. Suspected gastrointestinal or liver toxicant, neurotoxic, respiratory toxicant. Alters protein solubility. Likely to elevate levels of ammonia.

  • Animal Cells. Calf fetus, chick embryo, chick kidney, chicken egg, cow heart, dog kidney, duck egg, guinea pig embryo, horse blood, monkey kidney, monkey lung, mouse blood, pig blood, rabbit brain, sheep blood, etc. These are used in vaccine production lines. Residues are not completely purified out of the final packaged product. Contamination can introduce new pathogens.

  • Animal DNA. Yes, DNA from animals. Genetically modified viral, bacterial, yeast, and animal DNA. Can be incorporated into the recipient’s DNA and cause unknown genetic mutations. Your crazy uncle? Maybe

  • Antibiotics. Allergic reactions can range from mild to life threatening (anaphylaxis). Depletes glutathione. Can affect RNA and DNA activity. Side effects can include damage to kidneys and hearing loss. Listed antibiotics include Chlortetracycline, Dihydrostreptomycin, Gentamicin, Neomycin, Polymyxin B, and Streptomycin. Chlortetracycline appears to be excitotoxic.

  • Antifungals (Amphotericin B). Immediate allergic reactions can include fever, shaking, chills, hypotension, anorexia, nausea, vomiting, headache, dyspnea, and tachypnea. Damage to liver, kidney, and heart can also occur.

  • Benzethonium Chloride. Cytotoxic, neurotoxic, excitotoxic, and synergistically toxic. Suspected endocrine toxicant.

  • Beta-Propiolactone. A Carcinogen. Also a suspected gastrointestinal, liver, respiratory, skin and sense organ toxicant.

  • Detergents. Cytotoxic. Detergents cause cells to leak or explode by weakening their walls. This catastrophically mimics the membrane attack complex. This overlooked event can be particularly harmful. Ask yourself Why?

  • Dimethyl-beta-cyclodextrin. Increases permeability of cells and mitochondria. Increases pertussis toxin production. Effect of toxicants in live humans has not been explored.

  • Emulsifiers. Generally listed as Polysorbate 80 or 20, these chemicals are similar to detergents in their ability to increase cell permeability, damage, and bursting. After injection they can rapidly metabolize into sorbitol and ethylene oxide which is much more toxic than the original chemical. These polysorbates have been shown to cause dangerous, sometimes fatal effects, when injected through a needle. Changes in heart function can occur immediately. The blood-brain-barrier can be weakened and penetrated, followed by seizures and even death. Anaphylactic and other reactions can occur. Infants are particularly susceptible. These polysorbates also demonstrate synergistic toxicity with a wide range of chemicals.

  • Ethyl Green. Very toxic. Causes cell growth inhibition, mutation, and death.

  • Formaldehyde. AKA, embalming fluid. Well-known toxicant. Carcinogenic; linked to leukemia, brain, colon, and lymphatic cancer. Gastrointestinal, liver, immune system, nerve, reproductive system, and respiratory poison.

  • Free Amino Acids. Excitotoxic. May be listed as amino acids, asparagine, casamino acid, gelatin, hydrolyzed porcine gelatin, L-histidine, yeast extract, yeast protein. Also as monosodium glutamate, monosodium L-glutamate, glutamate, glutamic acid, potassium glutamate. In free form these have neurotoxic, mutagenic, teratogenic and reproductive effects. Reactions can range from mild to severe. Reaction times range from immediate to weeks later. Tied to ADHD.

  • Glutaraldehyde. Toxic; developmental, immune, reproductive, respiratory, skin or sense organ. Glutaraldehyde exposure causes amino acid, extracellular proteins and cell surfaces to bind to each other.

  • Hexadecyltrimethylammonium Bromide (AKA cetrimonium bromide). Teratogenic: an agent that causes malformation of an embryo. In other words: capable of interfering with the development of a fetus, causing birth defects. OK, try to justify the benefit of injecting THAT into a female

  • Human Aborted Fetal Tissue. Many aborted fetuses have been used in the development of ‘cell lines’ for the mass production of vaccines. Some amount of these ‘immortalized’ cells are present in the final packaged product. Examples include MRC-5, WI-38, RA27/3 (the RA27/3 strain of rubella virus was observed to induce brain cell death), WI-26 VA4, HEK-293, and IMR-90. At the outset PER.C6 was started for the sole purpose of vaccine development. The PER.C6 cell line is being promoted for use in flu, HIV/AIDS, tuberculosis, malaria, rabies, and cancer vaccines.

  • Hydrocortisone. Synthetic form of cortisol. Widely recognized as a major stress hormone, it also can disrupt fetal development and endocrine function, affect immune function, increase oxidative stress, and suppress adrenal function. It is synergistically toxic with dioxin where it has been shown to increase the incidence of cleft palate. It may also have a contributing effect in the onset of “metabolic syndrome”.

  • Iron Ammonium Citrate. An iron donor that can disrupt iron metabolism, impair immune function and increase oxidative damage.

  • Lactalbumin Hydrolysate. Added to growth culture during vaccine production. Can induce allergy to lactalbumin and to milk in general. May trigger an easier formation of amyloid fibrils associated with neurodegenerative diseases. Accelerates cell growth synergistically with yeast. Displays other various effects on immune system including altered blood clotting time, altered enzyme secretion, increased phagocytic activity, and enhanced tumor growth. Another source of excitotoxin.

  • Octoxynol 9 (or 10) and Triton X-100. Typically contain traces of the toxicants ethylene oxide, dioxane, C9 phenols, or glycol ether (AKA, anti-freeze). REALLY ask yourself Why?

  • pH Buffers. These control pH within a specific vaccine formula, but downstream effects on body fluids and tissues after injection have not been thoroughly researched. Local concentrations of Ca2+, Na+, and K+ ions can be altered once the buffers are no longer confined to the vaccine. Neurons are highly sensitive to slight changes in pH. Citric acid is excitotoxic and may harbor mercury. Sodium citrate is a strong blood anticoagulant that converts Ca2+ into calcium citrate, a process that increases absorption of aluminum and lead and contributes to excitotoxicity. It is a byproduct of citric acid manufacturing so may also harbor mercury depending on its source.

  • Phosphate buffers. Contain the element phosphorus. Phosphorus is an important component of all body tissues, plays a role in bone development, supports calcium metabolism, is a buffer for acid-base equilibrium, and is an element in various enzyme systems. Buffers containing phosphorus have the ability to affect various metabolic processes and can trigger or intensify excitotoxicity. There could be some precipitation of calcium phosphate in soft tissue (calcification). Overall these phosphate buffer agents appear less problematic than other ingredients, but they can still add stress to the system when administered. This example shows how exposure from the levels in a vaccine are of similar magnitude to what has shown harm in infants. Effects may be subtle and unobserved, however the timing and location of exposure can have an effect on other events. The elderly, young children, and patients with poor kidney function are at increased risk.

  • 2-Phenoxyethanol. AKA, Ethylene Glycol Monophenyl Ether (more anti-freeze). Various modes of toxicity including neuro, reproductive, and developmental.

  • Phenol. Toxic at all levels.

  • Phenol Red (phenolsulfonphthalein). An endocrine disruptor.

  • Sodium Bicarbonate (aka baking soda). A salt consisting of the Na+ ion and the bicarbonate HCO3-anion. At a cellular level this pair is critical in regulating pH, especially in the brain and central nervous system where sodium-bicarbonate transport has been shown to govern the function of neuron and glial cells, the production of myelin, and protection against excitotoxicity. People with immature or damaged nervous systems (infants, small children, people suffering toxic insult) are most at risk from the effects of free NaHCO3 received by injection.

  • Sodium borate (aka Borax). Neurotoxic and not meant for internal use. Infants are particularly susceptible especially with repeated exposure. Symptoms can be immediate but generally appear hours or days later. Symptoms include nausea, vomiting, diarrhea, flushed skin, changes in respiration/temperature/pulse, hyperactivity, CNS depression, mental confusion, lethargy, seizures, shock, metabolic acidosis, vascular collapse, and death. At the cellular level it interferes with DNA, RNA, and enzymes and causes cell death.

  • Sodium Deoxycholate. Causes cell death and symptoms such as burning, redness, and swelling. It has been shown to weaken the blood-brain barrier 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.

  • Sodium Hydroxide. Also known as caustic soda and lye. Corrosive to all body tissue, damage commences immediately. Indication that under certain conditions a lower concentration causes greater effect than higher concentration (hormesis). Depending on the source, it may be contaminated with mercury.

  • Sorbitol. Plays a vital step in the ‘polyol pathway’. The sudden injection of extra sorbitol can ruin the equilibrium of enzymes that regulate the conversion of glucose to fructose in a process associated with the onset of diabetes and its complications. Further, the polyol pathway is involved with a complex network of metabolic activities; disruption leads to a cascade of problems such as mitochondrial failure, cell apoptosis (cell death), and DNA fragmentation. In general, sorbitol induces cell hyperosmotic stress resulting in phosphorylation (uptake of phosphorus into cell), an important on/off switch regulating enzymes and signaling networks. Government record prominently states under Drug Warnings that sorbitol is not to be injected.

  • Sucrose. Disrupts immune function when injected directly into blood.

  • Thimerosal. Neurotoxic, mutagen, reproductive toxicant, carcinogen. Has an affinity for the brain, gut, liver, bone marrow and kidneys. Symptoms of mercury toxicity match those of autism. Note that thimerosal is extremely toxic by all routes of administration. There is no safe level of exposure.

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    Disclaimer. Note that this is by no means as yet a complete list. Nor, it cannot include other newer, unknown experimental excipients which are routinely used to replace excipients that are eventually admitted to be too dangerous to inject into humans (such as dangerous thimerisol was largely, but not completely, replaced by only slightly less dangerous aluminum). Never mind the contaminants that somehow get dumped into batches of vaccines that are eventually recalled after thousands are sickened

    For the CDCs list of vaccines summarizing their perspective on some of the excipients they contain, click on this link. Check the one at the very top of the list, loaded with much of the above crap and more. Really, why put yellow dye in a vaccine. Think about that

    As an example of what the CDC list of vaccine excipients avoids admitting, the following excerpt is from the CDCs breakdown of Glutaraldehyde, found minimally in the DTaP vax. A link to the source follows the excerpt for verification.

    Glutaraldehyde is used for a number of applications such as the following:

    • In embalming solutions
    • A biocide in metalworking fluids and in oil and gas pipeline
    • A disinfectant in animal housing
    • A hardening agent in the development of X-rays

    Health effects that may occur as a result of exposure to glutaraldehyde include but are not limited to the following:

    • Throat and lung irritation
    • Asthma and difficulty breathing
    • Contact and/or allergic dermatitis
    • Wheezing
    • Burning eyes and conjunctivitis

    Link to CDC Glutaraldehyde NIOSH Workplace Safety and Health Topic.

    Bonus link to Vaccine Ingredients — A Comprehensive Guide.

    If you have any questions, suggestions, requests, or proposals, you may either send us an email at jeb@vaccidemic.org or leave a comment at the bottom of this webpage.

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