New CDC Research Debunks Agency’s Assertion That Mercury in Vaccines Is Safe

New CDC Research Debunks Agency's Assertion That Mercury in Vaccines Is Safe
Source: GreenMedInfo.com
Sayer Ji
April 17, 2017

Originally published on EcoWatch.com.

The U.S. Environmental Protection Agency (EPA) and U.S. Food and Drug Administration (FDA) once again advised pregnant women to curb consumption of fish in order to limit fetal exposures to neurotoxic mercury. This warning raises the baffling query: How can the Centers for Disease Control and Prevention (CDC) justify its recommendations that pregnant women get flu shots which are laden with far more mercury than what’s found in a can of tuna?

The CDC has long answered that nettlesome question with the controversial claim that ethylmercury in vaccines is not toxic to humans. Now, two CDC scientists have published research decisively debunking that assertion. As it turns out, there is no “good mercury” and “bad mercury.” Both forms are equally poisonous to the brain.

The CDC studyAlkyl Mercury-Induced Toxicity: Multiple Mechanisms of Action, appeared last month in the journal, Reviews of Environmental Contamination and Toxicology. The 45-page meta-review of relevant science examines the various ways that mercury harms the human body. Its authors, John F. Risher, PhD, and Pamela Tucker, MD, are researchers in the CDC’s Division of Toxicology and Human Health Sciences, Agency for Toxic Substances and Disease Registry.

“This scientific paper is the one of most important pieces of research to come out of the CDC in a decade,”

Paul Thomas, M.D., a Dartmouth-trained pediatrician who has been practicing medicine for 30 years, said.

“It confirms what so many already suspected: that public health officials have been making a terrible mistake in recommending that we expose babies and pregnant women to this neurotoxin. I regret to say that I gave these shots to children. The CDC led us all to believe that it was perfectly safe.”

Among the findings of the CDC’s new study:

  • Methylmercury, the highly-regulated neurotoxin found in fish, and ethylmercury (found in medical products, including influenza and tetanus vaccines, ear drops and nasal sprays) are similarly toxic to humans. Methylmercury and ethylmercury share common chemical properties, and both significantly disrupt central nervous system development and function.
  • Thimerosal is extremely toxic at very low exposures and is more damaging than methylmercury in some studies. For example, ethylmercury is even more destructive to the mitochondria in cells than methylmercury.
  • The ethylmercury in thimerosal does not leave the body quickly as the CDC once claimed, but is metabolized into highly neurotoxic forms.

Despite this stark rejection of a decade of CDC safety assurances, CDC’s public relations machine is still bucking the new scientific consensus; the article concludes with a telling disclaimer in tiny font:

“The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the Agency for Toxic Substances and Disease Registry.”

CDC’s website continues to feature now discredited safety assurances.

“Baldly dismissing the danger to humans from ethylmercury, has long been a reckless gambit,” said J.B. Handley, a Portland, Oregon, businessman who believes that his son received debilitating injuries from a mercury vaccine.

“With this study, by its own scientists, the CDC has now edged into the realm of criminal endangerment.”

Handley, the founder of Generation Rescue, a vaccine safety advocacy group, condemns the CDC for misleading the medical establishment.

“The CDC knows that pediatricians and physicians rely on its public pronouncements when they make treatment decisions for their patients; how can we escape the conclusion that the agency is knowingly causing the poisoning of tens of millions of American children,” Handley stated.

For example, CDC’s webpage still parrots the now discredited industry canard that:

“Thimerosal contains ethylmercury, which is cleared from the human body more quickly than methylmercury, and is therefore less likely to cause any harm.”

However, the new study makes the opposite conclusion:

“Thimerosal is quickly metabolized in vivo (in a living organism) due to its reactions with protein and non-protein thiols … so the effects of thimerosal reported in numerous articles are very likely the result of exposure to the metabolite ethylmercury.”

Ignoring the agency’s own scientific evidence, the CDC’s webpage stubbornly insists that the “two types of mercury to which people may be exposed—methylmercury and ethylmercury—are very different.” The new CDC study directly contradicts this assertion, “There are many commonalities/similarities in the mechanisms of toxic action of methylmercury and ethylmercury …”

The study meticulously details identical toxicity pathways shared by both forms of mercury:

  • Both ethyl and methyl mercury cause DNA damage or impair DNA synthesis (Burke et al. 2006; Sharpe et al. 2012; Wu et al. 2008).
  • Both cause oxidative stress/creation of reactive oxygen species (Dreiem and Seegal 2007; Garg and Chang 2006; Myhre et al. 2003; Sharpe et al. 2012; Yin et al. 2007).
  • Both decrease glutathione activity, thus providing less protection from the oxidative stress caused by MeHg and EtHg (Carocci et al. 2014; Ndountse and Chan (2008); Choi et al. 1996; Franco et al. 2006; Mori et al. 2007; Muller et al. 2001; Ndountse and Chan 2008; Wu et al. 2008).
  • Both cause effects on cell division by damaging the spindle apparatus during mitosis (Burke et al. 2006; Castoldi et al. 2000; Gribble et al. 2005; Kim et al. 2007; Ou et al. 1999b; Machaty et al. 1999; Rodier et al. 1984).
  • Both MeHg and EtHg bind to the amino acid cysteine (Clarkson 1995; Wu et al. 2008).
  • Both MeHg and EtHg strongly inhibit the reacylation of arachidonic acid, thus inhibiting the reincorporation of this fatty acid into membrane phospholipids (Shanker et al. 2002; Verity et al. 1994; Zarini et al. 2006).
  • Both cause an increase in NOS, causing an overproduction of NO (Chen et al. 2003; Chuu et al. 2001; Shinyashiki et al. 1998).
  • Both disrupt glutamate homeostasis (Farina et al. 2003a, b; Manfroi et al. 2004; Mutkus et al. 2005; Yin et al. 2007).
  • Both alter intracellular calcium homeostasis (Elferink 1999; Hare et al. 1993;Kang et al. 2006; Limke et al. 2004b; Machaty et al. 1999; Marty and Atchison1997; Minnema et al. 1987; Peng et al. 2002; Sayers et al. 1993; Sirois and Atchison, 2000; Szalai et al. 1999; Tornquist et al. 1999; Zarini et al. 2006).
  • Both cause effects on receptor binding/neurotransmitter release involving one or more transmitters (Basu et al. 2008; Coccini et al. 2000; Cooper et al. 2003; Fonfria et al. 2001; Ida-Eto et al. 2011; Ndountse and Chan 2008; Yuan and Atchison 2003).

“This study is a nuclear bomb detonating over the CDC,” Boyd Haley, chairman emeritus of the University of Kentucky Chemistry Department, said. “It should be getting international, front page headlines.”

As one of the world’s leading authorities on mercury toxicity, Haley observed, “It’s a momentous rejection of a widely held medical orthodoxy dictating policy changes even more significant than the medical establishment’s reversals on thalidomide, calomel tooth powder, x-rays during pregnancy, or lead exposure to children. In each of these cases, thousands of children were injured or killed before an entrenched medical establishment was finally willing to abandon treatments that were unquestionably causing great harm.”

Ethylmercury vs. Methylmercury in Mass Poisonings

The revolutionary conclusions of the new CDC study actually reflect decades of work by mainstream independent scientists outside the agency. A rich scientific literature that emerged from accidental poisoning events has consistently documented—despite CDC’s official claims—that ethylmercury and methylmercury are equally toxic. In addition to the well-known Minamata and Iraq methylmercury-poisoning, many other large-scale food poisonings have occurred involving ethylmercury fungicides in Iraq in 1956 and 1960, in Pakistan in 1961, and in Russia in the 1960s as well. These episodes resulted in maladies ranging from basic tissue injury to heart and brain injury and even death.

Derban reported in 1974 on 144 cases of mercury poisoning from the use of ethylmercury fungicide on a southern Ghana state farm. Multiple other studies based on these poisoning events showed, as stated in a 1977 study by David Fagan, that the long-term neurological consequences produced by the “ingestion of either methyl or ethyl mercury-based fungicides are indistinguishable.”

1979 case report concerned a fifteen-year-old boy who had eaten the meat of a pig that had fed on ethylmercury fungicide−treated seed. Documented effects on the boy included debilitating brain damage and loss of coordination, with high toxicity for the brain as well as the spinal motor neurons, peripheral nerves, skeletal muscles, and heart muscle. The boy died about one month after becoming ill.

Ethylmercury’s use as pesticide was eventually banned in many countries, including the United States and those in the European Union, and for good reason: A 1977 study gauged ethylmercury chloride’s relative toxicity as a pesticide as the fifth most toxic of thirty substances tested, with a score of 12.7. That grade score almost matched that of DDT, at 14.2, an infamous pesticide banned in 1972.

In 1977 Fagan reported on 13 children suffering from exomphalos (a rare abdominal wall defect that allows the intestines to protrude from the abdomen) treated with gauze soaked applications of thimerosal to prevent infection. Of thirteen patients treated with thimerosal, 9 died. The authors tested mercury levels in the tissue of 8 of the children who died. They reported that “blood and tissue levels of mercury well above the threshold at which damage occurs in all other age groups, it is extremely unlikely that these infants escape neurological damage, which may be subtle.” One infant exposed to thimerosal and survived was later reported as being “restless, easily distracted, and not interested in schoolwork.” The authors recommended that “organic mercurial antiseptics should be heavily restricted or withdrawn from hospital use, as the fact that mercury readily penetrates intact membranes and is highly toxic seems to have been forgotten.”

Why Does the US EPA only Provide Guidelines for Exposure to Methylmercury and not Ethylmercury?

In 1995, based on research from outbreaks of poisonings and other research from the Faroe Islands and the Seychelles, the EPA established a safe “reference dose” for methyl mercury(RfD). An RfD is defined as “an estimate of a daily exposure to the human population (including sensitive subgroups) that is likely to be without an appreciable risk of adverse effects when experienced during a lifetime,” according to the EPA.

The EPA adopted for methylmercury an RfD of 0.1 microgram of mercury per kilogram of the individual’s body weight per day. Other health agencies set their own recommended limits for methylmercury exposure, including the FDA in 1979, the World Health Organization in 1989 and the US Agency for Toxic Substances and Disease Registry (ATSDR) in 1999. The highest of these limits was the WHO’s, at 0.47 microgram per kilogram of body weight per day.

In 1999 the US Congress directed the EPA to contract with the nonprofit, independent National Research Council (NRC) to prepare recommendations on an updated and appropriate RfD. The EPA commissioned the National Academy of Sciences (NAS) and the NRC to carry out a study on toxicological effects of methylmercury compounds. The goal was to review the process used by the EPA to establish national safety standards. The committee evaluated the literature, which demonstrated methylmercury compounds’ high toxicity to brain tissue, even at minute levels. The NAS ultimately agreed with the EPA‘s originally conceived RfD, which remains in place today. An RfD has never been established for ethylmercury.

The CDC has crossed ethical and perhaps even legal boundaries by purposefully blocking efforts by the National Institute of Environmental Health Science’s (NIEHS) National Toxicology Program (NTP) to test ethylmercury for toxicity – a process that would have lead to maximum exposure guidelines. In 2000, the FDA nominated thimerosal to the NTP for toxicity testing. However, CDC officials derailed the review telling the NTP committee that “There is a great concern within CDC about continued attacks from anti-vaccine groups questioning the integrity of CDC activities and recommendations regarding the use of thimerosal-containing vaccine.” In response to CDC pressure, the NTP put thimerosal on permanent deferred status. Thimerosal has, therefore, never been tested for safety or toxicity.

Ethyl Mercury Exposure Levels Based on Methyl Mercury Guidelines

A single Thimerosal-preserved flu vaccine contains 25 micrograms of ethylmercury. If the EPA RfD for ingested methylmercury is applied to this injected ethylmercury figure, an individual would have to weigh more than 250 kilograms (551 pounds) for the 25 microgram exposure to be considered safe. Back in the 1990s, a two-month-old child could have received 62.5 micrograms from three vaccines in a single doctor’s visit. Assuming the child weighed about 5 kilograms (11 pounds), he or she would have received 125 times the EPA RfD for methylmercury.

At least one study has suggested that the methylmercury RfD should be set lower for infants and also for fetuses. In 1995, Steven Gilbert and Kimberly Grant-Webster wrote:“Available information on the developmental neurotoxic effects of MeHg [methylmercury], particularly the neurobehavioral effects, indicates that the fetus and infant are more sensitive to adverse effects of MeHg. It is therefore recommended that pregnant women and women of childbearing age be strongly advised to limit their exposure to potential sources of MeHg. Based on results from human and animal studies on the developmental neurotoxic effects of methylmercury, the accepted reference dose should be lowered to 0.025 to 0.06 MeHg [microgram]/kg/day.”

What might this mean for a fetus today? We’ll take the low end of that estimate and apply it to an average 1.15-kilogram (2.54-pound) fetus at the start of the third trimester. A fetus exposed to 25 micrograms of mercury via a Thimerosal-preserved flu shot administered to its pregnant mother could be subject to 870 times the proposed lower reference dose.

Mainstream Science Suggests Ethylmercury is More Toxic than Methylmercury

New and old research support the caveat that “safe” levels of ethylmercury exposure might indeed be dramatically lower than the EPA’s RfD. A 2012 Italian study, for instance, showed that ethylmercury-containing Thimerosal diminished the viability of human cells in the lab at a concentration one-fiftieth that of methylmercury. By this measure, ethylmercury is 50 times as toxic as methylmercury to humans.

Japanese research on rats in 1968 showed that ethylmercury compounds, such as ethylmercuric chloride from which Thimerosal is made, clear the body more slowly than other mercury compounds including mercuric chloride and phenylmercuric chloride.

A book chapter in 1972 by Staffan Skerfving, an emeritus professor at Lund University in Sweden, reviewed literature on methylmercury versus ethylmercury, noting several instances where compounds of the latter appeared more toxic than the former in animal studies.

For example, ethylmercury chloride killed off half of a test population of mice—a classic “LD50” (lethal dose) study—within a week at a concentration of 12 milligrams of mercury per kilogram of body weight; methylmercury chloride’s LD50, meanwhile, lethal to half the mice was 14 milligrams. This study suggested that ethylmercury was twice as toxic.

Further examples abound. Pig studies by Tryphonas and Nielsen in 1973 showed that ethylmercury “proved much more toxic” than methylmercury. Meanwhile, another 1973 study that emerged from a 1971 international conference found the toxicity of ethylmercury compounds comparable to or even greater than that of methylmercury, as well as more persistent in the brain.

An advisory committee at the conference reported that the International Committee on Maximum Allowable Concentration for Mercury and Its Compounds grouped ethylmercury with methylmercury, and observed that accounts of human intoxication with ethylmercury have usually described neurological and other symptoms similar to those of methylmercury. The report noted that in studies of patients transfused with a commercial product of human plasma containing 0.01 percent Thimerosal, as well as in studies of mice injected with an ethylmercury solution, the increased level of inorganic mercury added to the mercury already existing in the body resulted in a “longer biological half-life of total mercury than that reported for methylmercury injection.”

Why do the CDC and WHO Report that Ethylmercury Exposure is Safe?

The WHO’s conclusion that ethylmercury is safer because of its “short” half-life may be based on observations that ethylmercury disappears from blood samples quicker than methylmercury. However, this tendency may be evidence not of ethylmercury’s comparative safety, but of its greater danger if, as science has suggested, ethylmercury is not leaving the body but simply migrating more rapidly to the organs, including the brain. Indeed, studies have shown that an ethylmercury compound’s short residence in the blood stems from its ability to more easily pass into the organs, where it can remain for long periods and possibly cause injury.

For example, Blair in 1975 dosed squirrel monkeys with intranasal saline or Thimerosal daily for six months, finding that, compared to the saline group, mercury concentrations in the Thimerosal group were significantly raised in the brain, liver, muscle, and kidney, though not in the blood. Although there were no signs of toxicity in the animals, Blair concluded that the “accumulation of mercury from chronic use of thiomersal-preserved medicines is viewed as a potential health hazard for man.”

Beyond a possibly greater capacity to have inorganic mercury accumulate in organs, Thimerosal also passes more easily from a mother’s bloodstream through the placenta into a developing baby than does methylmercury. That was the evaluation made in a 1983 review study by A. Leonard. In addition, a 1995 study demonstrated that both ethylmercury and methylmercury cause mutagenic changes at similar concentrations in bacterial cells.

The Twisted Saga of Pichichero

With these and other studies as background, an important study in humans took place in the early 2000s. The study, by Michael Pichichero of the University of Rochester Medical Center and published in The Lancet in 2002, lent some apparent scientific credence to the idea that ethylmercury is safer than methylmercury. Pichichero, who helped develop the HiB vaccine and previously received grants and honoraria as a consultant for other vaccine makers, did not declare these conflicts of interest in a statement in his paper, as required by The Lancet’s peer review rules. The Pichichero study assessed mercury levels in the blood, urine, and feces of forty infants ages six months or younger three to twenty-eight days after they had received Thimerosal-preserved vaccines (DTaP, HepB, and in some cases Hib). For comparison, twenty-one similar infants who received Thimerosal-free vaccines were also evaluated. Although infants who received Thimerosal-preserved vaccines had higher levels of mercury in their blood, urine, and feces than did the infants who received Thimerosal-free vaccines, the authors concluded that the levels of mercury detected were not greater than what is considered safe. Most of the mercury from the injected Thimerosal seemed to have left the children’s bloodstreams more rapidly than methylmercury found in the blood of those eating fish in previous studies; the researchers estimated a half-life of seven days for ethylmercury in the blood. Pichichero concluded that ethylmercury, therefore, did not remain in children’s bodies long enough to possibly cause damage.

Pichichero’s study immediately came under attack by internationally respected scientists in a 2003 letter to The Lancet by Neal Halsey, of the Institute for Vaccine Safety at Johns Hopkins Bloomberg School of Public Health, and Lynn Goldman, also of the Bloomberg School of Public Health. Halsey and Goldman pointed out that Pichichero and colleagues “did not measure the peak blood concentrations that occurred within hours after the injections.” The concentration listed for one child in the study of 20.55 nanomoles per liter was obtained five days post-vaccination. Assuming Pichichero’s own estimate of an ethylmercury half-life in the blood of seven days, the peak blood concentration for this child was 29.4 nanomoles per liter—exceeding the conventional safety threshold of 29.0 nanomoles per liter, and contradicting the study’s claim that “no children had a concentration of blood mercury exceeding 29 nmol/L.” The child in question had received 37.5 micrograms of ethylmercury rather than the possible maximum exposure of 62.5 micrograms. In the latter scenario, the child’s peak blood mercury concentration would have hit 48.3 nanomoles per liter.

Another child in the study registered a 7 nanomole per liter blood concentration 21 days post-vaccination; extrapolating backwards, this child’s peak mercury level might have reached 42 nanomoles per liter. Halsey and Goldman’s letter further pointed out that Pichichero seemed to have cherry-picked the children in the study—some already with no margin of safety for further mercury exposure—seemed to have come from a population with low background environmental and maternal exposure to methylmercury.

Soon after publication of Pichichero’s study, alarming new evidence emerged that ethylmercury lingers in the body. In an unpublished letter submitted to Pediatrics, Dr. Boyd Haley, then-chairman of the chemistry department at the University of Kentuck, and Mark Blaxill challenged Pichichero’s hypothesis that ethylmercury is quickly excreted. Pichichero and colleagues had measured the excretion levels of mercury in the stools of 22 healthy infants exposed to Thimerosal-containing vaccines. Pichichero’s estimated range for the infants aged two and six months was 23 to 141 nanograms per gram of stool (dry weight). Assuming the excretion rate reported by Pichichero, Blaxill and Haley demonstrated that it could take children with low excretion rates of mercury in their stool almost four years to eliminate a 187.5 microgram mercury burden from their bodies.

In 2006, Luis Maya and Flora Luna further debunked Pichichero’s conclusions. The authors pointed out that while Pichichero’s team had found ethylmercury to be excreted in appreciable quantities in the feces, the researchers did not study other body parts beyond the blood, such as the central nervous system. In agreement with Halsey and Goldman, Maya and Luna criticized Pichichero for neglecting to measure the peak serum levels of ethylmercury after the first hours of inoculation, though other investigations had documented substantially elevated blood concentrations in the first 48 to 72 hours after administration in pediatric vaccines. Maya and Luna also pointed out that the study was small and measured variables of pharmacokinetics (the actions of a drug within the body over time), so it was not designed to measure the biological effect of Thimerosal as a preservative.

Pichichero Redux: Yes, Ethylmercury Rapidly Leaves the Blood, but Not the Body. It Lodges in the Brain!

By then, other research had clarified that, while ethylmercury disperses quickly from the bloodstream, this is not evidence of safety. For example, a 2004 study by G. Jean Harry of the National Institute of Environmental Health Sciences noted that mice injected with Thimerosal accumulated mercury in both the brain and kidneys. “By seven days” post-treatment, the study authors wrote, “mercury levels decreased in the blood but were unchanged in the brain” compared to levels measured just 24 hours after treatment, indicating slow clearance.

The landmark study in this regard was conducted by the University of Washington’s Thomas Burbacher and published in 2005. The researchers compared mercury levels in the blood and brains of infant macaques injected with Thimerosal-containing vaccines with monkeys who ingested equal amounts of methylmercury hydroxide via a feeding tube. The former group of primates were exposed to 20 micrograms of ethylmercury per kilogram of body weight on the day they were born and when they were seven, 14, and 21 days old, which was estimated to be within the range of doses that children at different developmental stages were receiving in the United States. The dosing methods were selected to mimic the routes of exposure in humans who eat mercury-containing foods and receive mercury-containing vaccines.

Subsequent tests showed a faster disappearance of mercury from the bloodstream of Thimerosal-injected monkeys than from the methylmercury group. Total mercury amounts in the brain were also threefold less for the Thimerosal-treated monkeys. However, the Thimerosal-injected monkeys had a higher ratio of brain-to-blood levels of mercury than the methylmercury group. In general, the primates injected with Thimerosal in the Burbacher study retained twice the level of inorganic mercury—a breakdown product of Thimerosal that has been suggested to be responsible for the brain damage associated with methylmercury—in their brains as the methylmercury-exposed primates. While all seventeen monkeys given Thimerosal had “readily” detectable levels of inorganic mercury in their brains, only nine of the seventeen exposed to methylmercury had detectable levels. Burbacher cited previous research ranging the half-life of inorganic mercury in various brain regions of primates from 227 to 540 days. In either case, that is a long time period for the toxic element to remain, especially if at higher levels from ethylmercury deposition versus methylmercury.

Burbacher and his colleagues wrote in summary that “[methylmercury] is not a suitable reference for risk assessment from exposure to thimerosal-derived [mercury]” and that: Data from the present study support the prediction that, although little accumulation of [mercury] in the blood occurs over time with repeated vaccinations, accumulation of [mercury] in the brain of infants will occur. Thus, conclusion [sic] regarding the safety of thimerosal drawn from blood [mercury] clearance data in human infants receiving vaccines may not be valid, given the significantly slower half-life of [mercury] in the brain as observed in the infant macaques.

A more recent 2012 study by Croatian researchers took a similar approach as Burbacher’s study, but in suckling rats. That study also discredits CDC’s claims of ethylmercury’s comparative safety. Maja Blanusa and colleagues gave rat pups either Thimerosal or inorganic mercury three times in their first 11 days of life, mimicking human infant vaccination schedules. The scientists then assessed the total retention of mercury and excretion over six days. The Thimerosal-exposed rats showed higher mercury retention rates in their brains. Furthermore, these Thimerosal-exposed rats exhibited similar fecal excretion and much lower urinary excretion compared to the inorganic mercury-exposed rats. That second group also demonstrated higher retention rates of mercury in organs other than the brain.

Two additional studies in the last few years by researchers in Brazil and Germany show, again, that methylmercury in particular should not be considered summarily more dangerous than ethylmercury. The studies found that cells similarly take up both forms of mercury. The former, by Luciana Zimmermann and colleagues, showed in 2013 that the methyl- and ethylmercury entered cultured rat cells in roughly equal measure and display similar toxicities. The 2014 German study led by Christoph Wehe used novel laboratory techniques in concluding that methylmercury and ethylmercury in the form of Thimerosal accumulated in equal measure in a type of cultured human neural cell.

Overwhelmingly, the literature presents clear evidence that ethylmercury is invasive and persistent in the brain. Emerging evidence suggests that ethylmercury is more toxic than methylmercury, in direct contrast with the CDC’s historic position. It’s time for CDC’s public relations department to catch up with mainstream science. Since the World Health Organization (WHO relies mainly on CDC’s vaccine safety science, the CDC’s unscientific pronouncements endanger, not just U.S. children, but hundreds of millions of children around the world. Knowing what we now know, the U.S. Federal agencies and the WHO should follow the precautionary principle and phase out the use of thimerosal in all medical products, including vaccines.

Read More At: GreenMedInfo.com

Julie & The Boys: CDC, Merck, Vaccines

FakeNews
Source: NoMoreFakeNews.com | JonRappoport.wordpress.com
Jon Rappoport
April 24, 2017

I write this story now to remind people there are several titanic unresolved issues surrounding research fraud at the CDC, involving the MMR vaccine.

We all know about CDC whistleblower William Thompson, a long-time researcher at the CDC. Thompson still works there.

On August 27, 2014, he released a statement through his lawyer, Rick Morgan, in which he admitted research fraud.

Thompson confessed he and his CDC co-authors cooked the data in a key 2004 study, thereby exonerating the MMR vaccine from any blame in causing autism.

Thompson has never been subpoenaed by Congress to confess what he knows about this case.

But what about Stephen Kraling and Joan Wlochowski?

Who?

They’re two former Merck virologists who filed a qui tam suit against Merck, the manufacturer of the very same MMR vaccine.

The suit claims Merck defrauded the US government by selling the vaccine, under a federal contract, when Merck knew the mumps component of the vaccine was far less effective than advertised.

Of course, Merck disputed this claim, but on September 5th, 2014, Judge Jones, of the Federal District Court for the Eastern District of Pennsylvania, gave the green light for the suit to move forward.

Kraling and Wlochowski assert several levels of Merck fraud:

To achieve a slam-dunk success, Merck tested the effectiveness of the MMR vaccine against the version of the virus in the vaccine, rather than against the natural mumps virus a person would catch in the real world.

Merck irrelevantly and deceptively added animal antibodies to the test results, thus giving the false appearance of strong human immune response to the vaccine.

On top of that, Merck faked the quantitative results of the tests to which the animal antibodies had been added.

Here is where these two Merck whistle blowers and Thompson, the CDC whistle blower, intersect:

In 2004, according to a report I have seen, Thompson wrote a letter to CDC Director, Julie Gerberding, warning her that he was about to present troubling and sensitive data about the MMR vaccine at an upcoming conference on vaccines and autism.

Thompson’s meaning was clear. He had found a connection between the MMR vaccine and autism.

Gerberding never answered his letter, and Thompson’s presentation at that conference was canceled.

Gerberding left the CDC in 2009.

She moved on to become…

The president of Merck Vaccines, the manufacturer of the MMR vaccine.

Major media consider this a non-story, on the level of a can of overflowing garbage on a quiet street corner.

Well, they have to consider it a non-story. If they reported it and pressed it and dug deep into it, they could fracture the pillars of the entire vaccine establishment.

In order to get at the whole truth (or refute any of the charges raised in this article), Congress needs to hold hearings, and competent committee members need to question, at length, William Thompson, the two Merck whistle blowers, and Julie Gerberding.

I say the chance of that happening is close to zero. I’d love to be proven wrong, but I see no sign Congress is willing to step up to the plate.

Too many drug-company lobbyists, too much campaign money from the drug companies, too much fear of going up against entrenched “scientists” who keep claiming all vaccines are safe and effective.

We’ve heard, from sources other than President Trump, that he is going to order a task force to investigate vaccine safety. We’ll see if it happens.

Earlier this year, I wrote about a group of CDC employees who are anonymously chomping at the bit to expose criminal behavior at their agency.

They call themselves the Spider Group—Scientists Preserving Integrity, Diligence and Ethics in Research. They have penned a letter to the CDC’s chief of staff, Carmen S. Villar:

Here is the explosive accusation they make:

“We are a group of scientists at CDC that are very concerned about the current state of ethics at our agency. It appears that our mission is being influenced and shaped by outside parties and rogue interests. It seems that our mission and Congressional intent for our agency is being circumvented by some of our leaders. What concerns us most, is that it is becoming the norm and not the rare exception.”

“Some senior management officials at CDC are clearly aware and even condone these behaviors. Others see it and turn the other way. Some staff are intimidated and pressed to do things they know are not right.”

“We have representatives from across the agency that witness this unacceptable behavior. It occurs at all levels and in all of our respective units. These questionable and unethical practices threaten to undermine our credibility and reputation as a trusted leader in public health.”

Since this initial explosion, I have heard nothing from the Spider Group. Perhaps they are waiting for a signal from President Trump that it is safe to proceed.

There is too much waiting. Whistle blower William Thompson is waiting for Congress to subpoena him. Congress is sitting on its hands, waiting. The two Merck whistle blowers are waiting for their law suit to move forward.

Children’s futures and lives are on the line.

Every day that passes brings new vaccine damage.

Read More At: JonRappoport.wordpress.com
_______________________________________________________________

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

What if a mandatory penicillin vaccine were forced onto every child in America starting tomorrow?

Image: What if a mandatory penicillin vaccine were forced onto every child in America starting tomorrow?
Source: NaturalNews.com
S.D. Wells
April 10, 2017

Currently, the state of California requires all children to be force vaccinated with the entire schedule of CDC “recommended” vaccines in order to be able to exercise their right to attend public school and get an education. It doesn’t matter if any of those children are allergic to mercury, aluminum, polysorbate 80, African green monkey kidney cells, genetically modified bacteria, neomycin (an antibiotic), human serum albumin (other people’s blood), formaldehyde, monosodium glutamate (MSG), bovine extract, gelatin, calf serum, or sodium chloride. Every child must be injected with all of these ingredients, without being tested for allergies against them first, as they are all listed and contained in the CDC’s “excipient” list of vaccine ingredients, in case you have any doubts. How many other U.S. states will soon demand forced vaccination for all children?

Even though penicillin, an antibiotic about 5 to 10% of the U.S. population is allergic to, is not currently a vaccine ingredient, does it matter? Did you know many vaccines are made with a peanut oil extract, but it’s not listed because only “trace amounts” remain? Nearly 2 million U.S. children have severe peanut allergies. Coincidence? Are those trace amounts enough to cause severe allergic reactions? You bet they are, along with unnatural, violent immune system reactions to injecting human blood, monkey kidney cells, cow’s blood, chicken embryo and live viruses combined from different strains.

Extreme vaccine-induced allergic reactions occur when your immune system reacts to foreign proteins and chemicals lodged in muscle tissue or that cross the blood/brain barrier

Penicillin allergy occurs because certain children’s immune systems mistake the drug as a harmful substance, often because the drug is injected with several viruses, bacteria, chemical adjuvants, foreign proteins, human pooled blood samples, and other experimental excipients that have never been tested for safety, allergies or for their neurotoxic effects on humans. Children in America are guinea pigs, including infants and babies still in the womb. Mercury is toxic to humans at any level, even if only eaten or when it touches the skin. Imagine what’s happening when it’s shot directly into body tissue through a needle.

If the human body detects and identifies these chemicals, drugs, and foreign proteins as harmful substances, it develops antibodies to them, even if they are mixed with powerful antibiotics. The second and third time those same drugs and chemicals are injected into the child, the reaction can be violent, brain damaging, central nervous system damaging, and yes, sometimes lethal, just like with penicillin.

Why the massive autism epidemic in 2017? Do the math…

Since 5 to 10% of the U.S. population is allergic to penicillin, if you injected everyone today with a penicillin-loaded vaccine, millions of people would suffer a severe allergic reaction, and many would die. There are more than 300 million Americans. If just 2% had a lethal allergic reaction to a penicillin inoculation, that would equate to about 6 million deaths. That’s how many people were murdered in the Holocaust. Now if you injected 300 million Americans with mercury, aluminum, formaldehyde, polysorbate 80, MSG, and African green monkey kidney cells, and just 2% of those people had a severe allergic reaction where their immune systems went into shock and their brains were damaged by the neurotoxins, there would be about 6 million people with autism spectrum disorder (ASD).

A new government survey of parents suggests that 1 in every 45 children ages 3 through 17 have already been diagnosed with ASD. This number is much higher than the CDC estimate, and for good reason. There are approximately 80 million children in the U.S.A. now. That means there are about 2 million children diagnosed with some form of autism, and many, many others who are suffering from vaccine damage that’s not diagnosed as ASD. When will that number equal or surpass 6 million? Statistics show that every other child in America will have some form of autism by 2032 – that’s 40 million children and just 15 years from right now.

Nearly 4 million American kids today have either severe peanut allergies or autism–wonder why?

The next time those autistic children are injected with the same drugs and chemicals, including the mercury-loaded influenza vaccine, a.k.a. the “flu shot,” specific antibodies will flag the dangerous concoction once injected into muscle tissue and blood, and the chemicals released by this activity cause the signs and symptoms associated with severe and often lethal allergic reactions, just like with penicillin. Get it?

Signs and symptoms of allergic reactions to injecting vaccine ingredients like peanut oil, formaldehyde, MSG, sodium chloride, aluminum, human albumin, aborted fetal cells, monkey kidney cells, gelatin, neomycin and mercury include: skin rash, hives, itching, fever, swelling, shortness of breath, wheezing, anaphylaxis, central nervous system damage, brain damage, nausea, abdominal cramps, rapid pulse, drop in blood pressure, seizures, loss of consciousness, coma, and death. Some severe allergic reactions to vaccines occur days or weeks after the concoction is injected.

Ask your doctor if vaccines contain experimental excipients. Ask the nurse for the vaccine ingredients insert and read every ingredient aloud in front of the doctor and your child. You should be aware of the biggest medical fraud cover up in the history of medicine. Here’s what you can do right now to combat the insanity.

Watch the highly informative whistle-blowing interview with the directors of the controversial film VAXXED that exposes the CDC’s known link between vaccines (such as the MMR–measles, mumps, rubella combo jab) and autism:

There are far more vaccine-damaged children in America than chemical weapons-damaged children in Syria

Image: There are far more vaccine-damaged children in America than chemical weapons-damaged children in Syria
Source: NaturalNews.com
Mike Adams
April 8, 2017

By now, you are surely aware that the U.S. war machine, under President Donald J. Trump, has launched cruise missiles against the Syrian government. The emotionally-charged justification for all this is that “beautiful babies” were being killed by chemical weapons. While the pro-war factions of the establishment elite are celebrating the missile strike, virtually the entire independent media is convinced that the “chemical attack” narrative is little more than a convenient false flag to justify “regime replacement” activities desired by America’s deep state. Even Ron Paul and Paul Craig Roberts have both asserted this.

President Trump’s explanation for the attack included these words:

Assad choked out the lives of innocent men, women and children. It was a slow and brutal death for so many. Even beautiful babies were cruelly murdered in this very barbaric attack. No child of god should ever suffer such horror.

If you replace the word “Assad” with “CDC” or “the vaccine industry,” it all makes even more sense. Vastly higher numbers of children right here in America have been “cruelly murdered” in the “barbaric attack” of toxic vaccines than have ever been killed by chemical weapons in Syria.

I agree with the President that “No child of God should ever suffer such horror,” but I wonder when this President will start working to stop the chemical assault on America’s children that’s being waged every day by the vaccine industry.

Mercury in vaccines is a state-sponsored CHEMICAL WEAPON that’s used against America’s children every day

No chemical weapon should ever be deployed against any child: Not VX Nerve Gas, not Sarin Gas and not toxic, brain-damaging mercury. The destruction of biological tissue with devastating effect is accomplished by all three of those substances (and many more, including glyphosate herbicide). Yet mercury is the only chemical weapon that’s deliberately INJECTED into children with devastating effect. You might even call mercury a “biological cruise missile” attack on brain tissue.

On the science side, there’s no question whatsoever that mercury is extremely toxic to human neurology. Even the CDC’s own research has conclusively proven that mercury in vaccines is toxic to children. As I wrote in a Natural News article earlier this year, entitled Health Ranger exposes chemical violence of mercury vaccines: The “war on children” must be stopped:

The CDC is a criminal operation that preys upon innocent children using fraudulent science. The “Vaccine Holocaust,” as it is sometimes called, is a deliberate and widespread assault on children using chemical violence. This war on children must be brought to an end in the name of compassion, sanity and legitimate science (not the fraudulent corporate science pushed by vaccine companies and the corrupt CDC).

Right now, mercury is still used in vaccines given to children and expectant mothers in the United States. This practice is barbaric, highly unethical and stands in horrific opposition to all the known science on the neurotoxicity of mercury. Those engaged in the continued pushing of mercury vaccines onto children are knowingly taking part in the most gruesome and dishonest medical science cover-up in the history of our world. It is time that parents, citizens, independent scientists and compassionate protectors of life took a stand against the child poisoners who are pushing mercury vaccines that cause permanent neurological disorders in children (including autism in some children).

This is why I continue to remind America that Vaccine Injury Denialism is the denial of fundamental human dignity.

Continue Reading At: NaturalNews.com

How many African Green Monkeys are infected, euthanized and then organ harvested each year to make FDA-approved vaccines?

[Editor’s Note]

For those that think this is a joke, this very document at the CDC’s very own website shows this, and many other toxins within vaccines.  This is why its imperative people do their research, because if people really knew what vaccines had, they’d think they woke up in another reality.

Image: How many African Green Monkeys are infected, euthanized and then organ harvested each year to make FDA-approved vaccines?
Source: NaturalNews.com
Ethan Huff
March 26, 2017

Now that it’s been proven that vaccine manufacturers harvest kidney cells from African Green Monkeys to produce vaccines that are injected into children, many are now wondering just how many of these monkey are captured, euthanized, and processed into vaccine ingredients each year to make these FDA-approved poison jabs?

As you may recall, Natural News was falsely accused of spreading “fake news” after breaking the story on African Green Monkey kidney cells, and other horrific ingredients, being used in the manufacture of vaccines. For merely publishing the ingredients listed on the vaccine package inserts that manufacturers are required to provide with their vaccines, Natural News faced an unrelenting barrage of fact-less criticism.

Not long after, though, it was realized that Natural News was telling the truth: these ingredients are, indeed, being used in childhood vaccines, and many parents aren’t aware of this fact because their doctors and pediatricians aren’t showing them the vaccine package inserts. Now the outrage is going in the other direction, as it should, because people are realizing that they’ve been lied to by their government. (RELATED: You can stay informed on important vaccine issues by visiting Vaccines.news.)

“As Natural News correctly reported, one of the many animal-derived ingredients used in vaccines and openly admitted by the CDC is African Green Monkey kidney cells,” writes Mike Adams, the Health Ranger. “Apparently, this realization was just too much for the scientifically illiterate media (and wholly dishonest vaccine pushers) who insisted it couldn’t possibly be true.”

You can see the list of ingredients yourself, published by the CDC, at this Natural News article link.

Parents: are you aware of all the horrible things being injected into your children?

Knowing that millions of vaccine are produced and administered every single year for injection into children, it boggles the mind to consider just how many of these African Green Monkeys are being subjected to death in order to manufacture them. The number has to be at least into the thousands, though no official number has been released by the CDC.

Many of these same vaccines also contain cells from aborted human fetal tissue, which sheds a whole new light on Planned Parenthood’s illegal baby harvesting scheme that involved selling aborted baby body parts to biotechnology companies for use in manufacturing “medicines.” It is now abundantly obvious that Planned Parenthood was trafficking those baby body parts for potential use in vaccine manufacture.

This is in addition to all the viruses, heavy metals, chemical preservatives, food colorings, and other toxic ingredients used in making vaccines. Children today are being injected with some of the most disturbing and poisonous substances known to mankind, and very few people seem at all concerned with what’s going on.

It’s probably because so many people don’t even know what’s going on, thanks to the mainstream media’s dereliction of duty in reporting on this important subject. Every parent should be required to peruse a vaccine package insert before injecting his or her child with a vaccine, and yet this is rarely the case.

Most doctors fail to inform parents about the presence of both human and animal tissue in their children’s “medicine,” for instance. They rarely mention the use of toxic mercury (thimerosal) in vaccines, or other noxious ingredients like aluminum, genetically-modified (GM) byproducts, cow blood, chemical solvents, and more. These additives are certifiably NOT safe, and they serve no beneficial purpose for those into whom they’re being injected.

“Several vaccines currently available in the United States were developed using the Vero cell line, started from African green monkey kidney cells,” explains The History of Vaccines.

These include:

• Rotavirus vaccines (Rotarix by GlaxoSmithKline and RotaTeq by Merck & Co.)
• Polio vaccine (IPOL by Sanofi Pasteur)
• Smallpox vaccine (ACAM2000 by Sanofi Pasteur)
• Japanese encephalitis vaccine (Ixiaro by Intercell)

Read More At: NaturalNews.com

Sources for this article include:

NaturalNews.com

HistoryOfVaccines.org

One More Reason Never To Trust The CDC

corruption3
Source: NoMoreFakeNews.com | JonRappoport.wordpress.com
Jon Rappoport
March 12, 2017

CBS has published the names of sites they claim are fake news. Well, what about CBS itself?

Unless you’ve been living in a cave, you’re aware that a film, Vaxxed, has been showing in theaters across America and overseas—and audiences are stunned by its revelations.

Vaxxed exposes a huge scandal at the CDC, where a long-time researcher, William Thompson, confessed (2014) that he and colleagues committed gross fraud in a study of the MMR vaccine.

Thompson admitted the evidence showed the vaccine led to a higher risk of autism in children—but that finding was intentionally buried, and the vaccine was given a free pass.

Of course, mainstream reporters have been mercilessly attacking Vaxxed, and a segment of the population finds it impossible to believe that the CDC would ever commit this kind of fraud.

So, as a mind-changer, let me take you back to the late summer of 2009, and the Swine Flu epidemic, which was hyped to the sky by the CDC. The Agency was calling for all Americans to take the Swine Flu vaccine. Remember?

The problem was, the CDC was concealing another scandal.

At the time, star CBS investigative reporter, Sharyl Attkisson, was working on a Swine Flu story. She discovered that the CDC had secretly stopped counting cases of the illness—while, of course, continuing to warn Americans about its unchecked spread.

Understand that the CDC’s main job is counting cases and reporting the numbers.

What was the Agency up to?

Here is an excerpt from my 2014 interview with Sharyl Attkisson:

Rappoport: In 2009, you spearheaded coverage of the so-called Swine Flu pandemic. You discovered that, in the summer of 2009, the Centers for Disease Control, ignoring their federal mandate, [secretly] stopped counting Swine Flu cases in America. Yet they continued to stir up fear about the “pandemic,” without having any real measure of its impact. Wasn’t that another investigation of yours that was shut down? Wasn’t there more to find out?

Attkisson: The implications of the story were even worse than that. We discovered through our FOI efforts that before the CDC mysteriously stopped counting Swine Flu cases, they had learned that almost none of the cases they had counted as Swine Flu was, in fact, Swine Flu or any sort of flu at all! The interest in the story from one [CBS] executive was very enthusiastic. He said it was “the most original story” he’d seen on the whole Swine Flu epidemic. But others pushed to stop it [after it was published on the CBS News website] and, in the end, no [CBS television news] broadcast wanted to touch it. We aired numerous stories pumping up the idea of an epidemic, but not the one that would shed original, new light on all the hype. It was fair, accurate, legally approved and a heck of a story. With the CDC keeping the true Swine Flu stats secret, it meant that many in the public took and gave their children an experimental vaccine that may not have been necessary.

—end of interview excerpt—

I’ll add a few details. It was routine for doctors all over America to send blood samples from patients they’d diagnosed with Swine Flu, or the “most likely” Swine Flu patients, to labs for testing. And overwhelmingly, those samples were coming back with the result: not Swine Flu, not any kind of flu.

That was the big secret. That’s what the CDC was hiding. That’s why they stopped reporting Swine Flu case numbers. That’s what Attkisson had discovered. That’s why she was shut down.

But it gets even worse.

Because about three weeks after Attkisson’s findings were published on the CBS News website, the CDC, obviously in a panic, decided to double down. If one lie is exposed, tell an even bigger one. A much bigger one.

Here, from a November 12, 2009, WebMD article is the CDC’s response: “Shockingly, 14 million to 34 million U.S. residents — the CDC’s best guess is 22 million — came down with H1N1 swine flu by Oct. 17 [2009].” (“22 million cases of Swine Flu in US,” by Daniel J. DeNoon).

Are your eyeballs popping? They should be.

In the summer of 2009, the CDC secretly stops counting Swine Flu cases in America, because the overwhelming percentage of lab tests from likely Swine Flu patients shows no sign of Swine Flu or any other kind of flu.

There is no Swine Flu epidemic.

Then, the CDC estimates there are 22 MILLION cases of Swine Flu in the US.

So…the premise that the CDC would never lie about important matters like, oh, a vaccine increasing the risk of autism…you can lay that one to rest.

The CDC will lie about anything it wants to. It will boldly go where no person interested in real science will go.

It will completely ignore its mandate to care about human health, and it will get away with it.

And CBS will conveniently forget how it aided and abetted the CDC, by censoring real news, and instead opted for egregious and titanic fake news.

Read More At: JonRappoport.wordpress.com
_______________________________________________________________

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

CDC Document Bombshell Reveals List Of All Vaccine Excipients, Including “African Green Monkey Kidney Cells” & Fibroblast Cells From Aborted Human Fetuses … See The Complete List

[Editor’s Note]

For those that think that the ingredients mentioned in the above title are ludicrous, or this is a joke, it is not.  The ingredients mentioned can be verified from on the CDC’s website, in this particular file:

https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf

Image: CDC document bombshell reveals list of all vaccine excipients, including “African Green Monkey Kidney Cells” and fibroblast cells from aborted human fetuses … see the complete list
Source: NaturalNews.com
Mike Adams
March 7, 2017

Almost no one has any real idea what’s found in vaccines. When they allow themselves to be injected with vaccines, they’re oblivious to the fact that they are being injected with aborted human fetus cell lines or African Green Monkey kidney pus cells harvested from infected, disease primates. (See proof from the CDC, below.)

Yet, astonishingly, the CDC openly admits to all this (and more). In a PDF posted on the CDC website entitled “Vaccine Excipient & Media Summary,” the CDC lists all the excipients currently used in vaccines being injected into adults and children across the United States. The CDC’s list, current as of January 6, 2017, was “extracted from manufacturers’ package inserts,” according to the CDC.

The complete list is found in this CDC document (PDF). In case the CDC removes it — because they’ve been known to suddenly “memory hole” documents they don’t want the public to see — we’ve also posted a copy at the Natural News servers (PDF).

The WI-38 cell line is widely known to be “derived from lung tissue of an aborted white (caucasian) female fetus,” as even the pro-vaccine Wikipedia website admits. As the Coriell Institute for Medical Research explains about the MRC-5 cell line / WI-38:

The MRC-5 cell line was developed in September 1966 from lung tissue taken from a 14 week fetus aborted for psychiatric reason from a 27 year old physically healthy woman. The cell morphology is fibroblast-like. The karyotype is 46,XY; normal diploid male. Cumulative population doublings to senescence is 42-48. G6PD isoenzyme is type B.

The human fetal tissue cells have become such an issue of outrage that even the Vatican has issued a statement concerning their use, in which they address, “vaccines containing live viruses which have been prepared from human cell lines of fetal origin, using tissues from aborted human fetuses as a source of such cells.” You can find the Vatican’s response at this link, in which they discuss the moral and ethical issues of “The principle of licit cooperation in evil.”

Below, you’ll find the complete list published by the CDC, de-duplicated and sorted alphabetically. Notice that these ingredients include toxic metals (aluminum salts), bizarre animal cells from humans, monkeys, cows, pigs and chickens, ingredients derived from GMOs, the radioactive element barium, artificial coloring chemicals, excitotoxins such as glutamate, chemical cleansing agents (Triton X-100), dangerous bacterial strains (E.coli), toxic chemicals such as glutaraldehyde, thimerosal (mercury) and much more.

No one can refute any of this because it’s admitted by the CDC itself.

More analysis of the toxicity of these ingredients will be published at Vaccines.news and Natural News.

Here’s what happens to some children when they’re injected with these toxins:

vaxd

The complete list of vaccine excipients published by the CDC, current as of January 6, 2017

betapropiolactone

CTAB (cetyltrimethylammonium bromide)

formalin

L-cystine

2-phenoxyethanol

a continuous line of monkey kidney cells

acetone

African Green Monkey kidney (Vero) cells

alcohol

aluminum hydroxide

aluminum phosphate

aluminum salts

amino acid supplement

amino acids

amino acids solution

aminoglycoside antibiotic

ammonium sulfate

ammonium sulfate aluminum phosphate

amorphous aluminum hydroxyphosphate sulfate

amphotericin B

anhydrous lactose

anti-foaming agent

arginine

ascorbic acid

asparagine

baculovirus and cellular DNA

baculovirus and Spodoptera frugiperda cell proteins

barium

benzethonium chloride

beta- propriolactone

beta-propiolactone

bovine albumin

bovine calf serum

bovine serum

bovine serum albumin

calcium carbonate

calcium chloride

calf bovine serum

Calf serum

calf serum and lactalbumin hydrolysate

carbohydrates

casamino acids

casamino acids and yeast extract-based medium

casein

castor oil

cell culture media

cellulose acetate phthalate

cetyltrimethlyammonium bromide

chick embryo cell culture

chicken fibroblasts

chlortetracycline

citric acid

citric acid monohydrate

CMRL 1969 medium supplemented with calf serum

complex fermentation media

concentrated vitamin solution

CRM197 carrier protein

CY medium

cystine

D- fructose

D- glucose

defined fermentation growth media

deoxycholate

dextran

dextrose

dibasic potassium phosphate

dibasic sodium phosphate

dimethyl-beta-cyclodextrin

dimethyl-beta-cyclodextrin. glutaraldehyde

disodium phosphate

disodium phosphate dihydrate

D-mannose

DNA

dried lactose

Dulbecco’s Modified Eagle Medium

Dulbecco’s Modified Eagle’s Medium

E. coli

Eagle MEM modified medium

EDTA (Ethylenediaminetetraacetic acid)

egg protein

egg proteins

ethylenediaminetetraacetic acid (EDTA)

FD&C Yellow #6 aluminum lake dye

Fenton medium containing a bovine extract

ferric (III) nitrate

fetal bovine serum

formaldehyde

Franz complete medium

galactose

gelatin

gentamicin sulfate

glutamate

glutaraldehyde

Glycerin

guinea pig cell cultures

HEPES

hexadecyltrimethylammonium bromide

histidine

histidine buffered saline.

host cell DNA

host cell protein

human albumin

human diploid cell cultures (MRC-5)

human diploid cell cultures (WI-38)

human embryonic lung cell cultures

human serum albumin

human-diploid fibroblast cell cultures (strain WI-38)

hydrocortisone

hydrolyzed casein

hydrolyzed gelatin

hydrolyzed porcine gelatin

inorganic salts

iron ammonium citrate

isotonic sodium chloride

kanamycin

L-250 glutamine

lactalbumin hydrolysate

lactose

L-histidine

lipids

L-tyrosine

M-199 without calf bovine serum

Madin Darby Canine Kidney (MDCK) cell protein

magnesium stearate

magnesium stearate. gelatin

magnesium sulfate

maltose

MDCK cell DNA

Medium 199 without calf serum

microcrystalline cellulose

mineral salts

modified culture medium containing hydrolyzed casein

modified Latham medium derived from bovine casein

modified Mueller and Miller medium

modified Mueller and Miller medium (the culture medium contains milk- derived raw materials [casein derivatives])

modified Mueller’s growth medium

modified Mueller-Miller casamino acid medium without beef heart infusion

modified Mueller’s media which contains bovine extracts

modified Stainer-Scholte liquid medium

monobasic potassium phosphate

monobasic sodium phosphate

monosodium glutamate

monosodium L-glutamate

monosodium phosphate

MRC-5 cells

MRC-5 cells (a line of normal human diploid cells)

MRC-5 diploid fibroblasts

MRC-5 human diploid cells

Mueller Hinton casein agar

Mueller’s growth medium

neomycin

neomycin sulfate

non-viral protein

nonylphenol ethoxylate

normal human diploid cells

octoxynol-10 (TRITON X-100)

octylphenol ethoxylate (Triton X-100)

ovalbumin

ovalbumin neomycin

phenol

phenol red

phenol red indicator

phosphate buffer

phosphate-buffered saline solution

plasdone C

polacrilin potassium

polydimethylsiloxane

polygeline (processed bovine gelatin)

polymyxin

polymyxin B

polymyxin B sulfate

polysorbate 20

polysorbate 20 (Tween 20)

polysorbate 80

polysorbate 80 (Tween 80)

potassium aluminum sulfate

potassium chloride

potassium glutamate

potassium phosphate

potassium phosphate dibasic

potassium phosphate monobasic

potassium phosphate potassium chloride

protamine sulfate

protein other than HA

recombinant human albumin

saline

semi-synthetic media

semi-synthetic medium

sodium bicarbonate

sodium borate

sodium carbonate

sodium chloride

sodium citrate

sodium citrate dehydrate

sodium deoxycholate

sodium dihydrogen phosphate dihydrate

sodium EDTA

sodium hydrogenocarbonate

sodium hydroxide

sodium metabisulphite

sodium phosphate

sodium phosphate dibasic

sodium phosphate monobasic monohydrate

sodium phosphate-buffered isotonic sodium chloride

sodium phosphate-buffered isotonic sodium chloride solution

sodium pyruvate

sodium taurodeoxycholate

sorbitan trioleate

sorbitol

soy peptone

soy peptone broth

squalene

Stainer-Scholte medium

sterile water

succinate buffer

sucrose

sugars

synthetic medium

thimerosal

thimerosal (multi- dose vials)

thimerosal (multi-dose vials)

tris (trometamol)-HCl

Triton X-100

uracil

urea

VERO cells

vero cells (a continuous line of monkey kidney cells)

vero cells [DNA from porcine circoviruses (PCV) 1 and 2 has been detected in RotaTeq. PCV-1 and PCV-2 are not known to cause disease in humans.]

vitamins

Watson Scherp casamino acid media

Watson Scherp media containing casamino acid

WI-38 human diploid lung fibroblasts

WI-38 human diploid lung fibroblasts MRC-5 cells

xanthan [Porcine circovirus type 1 (PCV-1) is present in Rotarix. PCV-1 is not known to cause disease in humans.]

yeast extract

yeast protein

α-tocopheryl hydrogen succinate

β-propiolactone

Read more At: NaturalNews.com