Archive for the ‘vaccines’ Category

Examining RFK Jr.’s Claim That The CDC “Owns Over 20 Vaccine Patents” (It’s Actually Over 50)

Although this was written in 2017, it’s an important reminder that the CDC has severe conflicts of interest regarding vaccines and that they are not to be trusted.  Please educate yourself.

https://www.greenmedinfo.com/blog/examining-rfk-jrs-claim-cdc-owns-over-20-vaccine-patents

Examining RFK Jr.’s claim that the CDC “Owns over 20 vaccine patents.”

Examining RFK Jr.'s claim that the CDC “Owns over 20 vaccine patents.”

Mr. Kennedy is in very safe territory by reporting that the CDC has over 20 patents that create vast, undisclosed conflicts of interests in vaccine safety.

This past week, President-Elect Trump invited Robert F. Kennedy Jr. to discuss Mr. Kennedy leading a vaccine safety commission.  The mainstream media coverage of the meeting was widespread and furious. 

The vaccine industry and its media lap dogs do not want their corruption exposed in any official forum, and they have pointed their fury at Mr. Trump and Mr. Kennedy. 

We have seen a great deal of media on Kennedy and his vaccine safety and corruption claims in the last week.  The nice thing about that is this – because he has been in the mercury fight for so long, and started investigating the claims of moms of vaccine injured children more than a decade ago, his coverage has returned the spotlight to the corruption that was uncovered in the early days of the realization that the vaccine program was hurting our kids.

One of these old pieces of information that has made its way back into the discussion because of Mr. Kennedy’s media attention is the claim that, “The CDC owns over 20 vaccines patents.”

My vaccine safety and corruption research began shortly after my son was vaccine injured in 2003, and I have heard this claim circulated since I began advocacy in this arena, but I have never seen any evidence for this claim.

In 2003, UPI reporter Mark Benjamin wrote an in depth piece on the conflicts of interest (COI) in vaccine safety entitled, “UPI Investigates: The vaccine conflict.”  We have Mr. Benjamin to thank for bringing the patents and COIs held by the members of the CDC Advisory Committee on Immunization Practices, including Dr. Paul Offit, to the public’s attention, and for documenting the early years of Offit’s increasingly absurd claims.  In this article, Offit asserts that holding vaccine patents, being funded by Merck and having Merck buy and distribute, to physicians, his book extolling the virtues of vaccines, does not compromise his objectivity as a member of the committee that determines what is and is not sound vaccine practice:

“When asked, members of the committee told UPI their potential conflicts do not affect their judgment.

“I am probably just the kind of person you are talking about,” said Paul Offit, chief of infectious diseases at the Children’s Hospital of Philadelphia, who was a committee member until last month. At the same time, he shared a patent for another rotavirus vaccine. Merck has funded Offit’s research for 13 years.

“I am a co-holder of a patent for a (rotavirus) vaccine. If this vaccine were to become a routinely recommended vaccine, I would make money off of that,” Offit said. “When I review safety data, am I biased? That answer is really easy: absolutely not.”
 

“Is there an unholy alliance between the people who make recommendations about vaccines and the vaccine manufacturers? The answer is no.’”
 

Merck bought and delivers copies of Offit’s book, “What Every Parent Should Know About Vaccines,” to American doctors. The book has a list price of $14.95.
 

“Merck Vaccine Division is pleased to present you with a copy of the recent publication, ‘What Every Parent Should Know about Vaccines,'” says a Dear Doctor letter from Merck. “The authors designed the book to answer questions parents have about vaccines and to dispel misinformation about vaccines that sometimes appears in the public media.”
 

Offit said he does not know how many copies of his book Merck purchased. “I don’t have any control over that,” he said.”
 

I encourage you to read the entire article.

However, the specifics and number of CDC vaccine patents are not reviewed there. 

Mr. Kennedy repeated the claim last month in an interview with EcoWatch saying, “The CDC is a subsidiary of the pharmaceutical industry. The agency owns more than 20 vaccine patents and purchases and sells $4.1 billion in vaccines annually.”  Again, no source.

I have been around long enough to know that vaccine claims have to be checked and rechecked.  And since this is a very old claim, one that I would like to be able to state (if it is true), I decided to review it.

I am fortunate to have, as one of my partners in advocacy, fellow autism parent Mark Blaxill, an Intellectual Property expert who has been employed by billion dollar corporations to manage their patents.  Blaxill was the man who found out that HHS, through NIH, owns patents on all HPV vaccines, and receives a percentage of the profits for each dose of Gardasil and Cervarix administered anywhere in the world.  He published the stunning revelation in a detailed three part expose entitled, “A License to Kill? Part 1: How A Public-Private Partnership Made the Government Merck’s Gardasil Partner.”

When I contacted Blaxill to ask how to run a patent search, he was kind enough to do it for me.  He found 57 granted US patents with the CDC listed as an assignee. You can see the search results here.

Upon cursory review of the patents, I found that one did not seem applicable to vaccination, but merely referenced an article on vaccination.  That leaves us with 56 CDC patents to scrutinize.

Here is what I found.

Does this seem like a public health agency making “independent” vaccine recommendations, or a private company with an impressive portfolio to which one might look for investment opportunities?

The CDC is reputed to be an independent government agency making vaccine recommendations to the public, only for the public good.  They are the agency charged with vaccine safety oversight, via their Immunization Safety Office.

Here is how the office describes its charge:

“CDC’s Immunization Safety Office plays a vital role in ensuring our nation’s vaccine safety.

Sound immunization policies affecting children and adults in the U.S. depend on continuous monitoring of the safety and effectiveness of vaccines.  CDC uses many strategies to assess vaccine safety, to identify health problems possibly related to vaccines, and to conduct studies that help determine whether a health problem is caused by a specific vaccine. CDC also works with other federal government agencies and other stakeholders to determine the appropriate public health response to vaccine safety concerns and to communicate the benefits and risks of vaccines.

The Immunization Safety Office regularly reports on vaccine safety monitoring findings and any concerns to CDC’s Advisory Committee on Immunization Practices (ACIP). This advisory group develops the recommended vaccine schedule for children and adults in the U.S.  ACIP considers the safety and effectiveness of vaccines before making recommendations to the vaccine schedule or changing recommendations for vaccine use.”


Note that they proudly state that they report to the ACIP – the same committee on which Paul Offit infamously served, as if this reporting somehow adds legitimacy to their vaccine safety work.  The same committee that Congress has excoriated for their long history of conflicts of interests.
Nowhere on the CDC’s web site can I find the disclosure that the agency is a profit partner with the vaccine makers for whom it is supposed to be providing safety oversight.

Mr. Kennedy is in very safe territory by reporting that the CDC has over 20 patents that create vast, undisclosed conflicts of interests in vaccine safety.  He is understating the problem by more than half.

This brief look at current patents held by the CDC deserves an in-depth review to determine exactly what current financial relationships with vaccine makers now exist and  what the current impact those revenue streams are likely having on vaccine safety positions.  Furthermore, one must closely look at the financial relationships between the CDC and vaccine makers it is currently courting, to include the potential exploitation of new patents for financial gain. These are merely a few  lines of inquiry, among hundreds, needing to be examined and why the potential RFK commission on vaccine safety must be impaneled.

No wonder the vaccine industry (and let’s not kid ourselves, CDC IS the vaccine industry) and their media outlets are fighting with such a fury to prevent the #RFKcommission from being formed.

Fortunately, Mr. Kennedy has already said he will fight this corruption against our children until his last breath, and we seem to have a new president who doesn’t care what Pharma and the mainstream media throw at him.  There is more than 20 years’ worth of documented abuse and corruption in the vaccine program that, if properly examined, would at the very least force reforms that would drastically reduce the profits of the industry.

The vaccine business is currently a $30 billion per year industry in which organizations like the World Health Organization have urged increased investment, projecting that it will become a $100 billion per year industry by 2025.  Thus, it is evident that the CDC and their business partners need the public to not only be okay with the 69 doses of recommended childhood vaccines, but to begin to adhere to the additional 100 plus doses of vaccines recommended by the new adult schedule, and to be ready to inject their families with the additional 271 vaccines in the development pipeline.

That profit boom can’t happen if the corruption in the industry, and the vast, unassessed damage that it has done to the health of children (and now adults) is laid open for all to finally see.  The $30 billion per year industry will become a sub $10 billion per year industry, with a cap on how much it can make.  Because there is a cap on how much the human body can process.

We must continue to press the Trump administration for comprehensive vaccine safety review and reform, including the universal right to forgo any and all vaccines without coercion.

Without a White House to ignore CDC’s abuses and run interference with the American public, the corrupt vaccine industry may be turning into a paper tiger, and its media simply a powerless crowd of bullies with a megaphone, broadcasting “sound and fury signifying nothing.”
 

Vaccination Research Dashboard

For evidence-based research on vaccinations, visit the GreenMedInfo.com Research Dashboard.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of GreenMedInfo or its staff.

 

AstraZeneca COVID-19 Vaccine Trial Put on Hold Due to Spinal Inflammation in Participant

https://www.statnews.com/2020/09/09/astrazeneca-covid19-vaccine-trial-hold-patient-report/

The participant who triggered a global shutdown of AstraZeneca’s Phase 3 Covid-19 vaccine trials was a woman in the United Kingdom who experienced neurological symptoms consistent with a rare but serious spinal inflammatory disorder called transverse myelitis, the drug maker’s chief executive, Pascal Soriot, said during a private conference call with investors on Wednesday morning.

The woman’s diagnosis has not been confirmed yet, but she is improving and will likely be discharged from the hospital as early as Wednesday, Soriot said.  (See link for article)

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**Comment**

The clinical trail was also stopped in July as well due to a participant developing neurological symptoms.  They state she was diagnosed with MS and it was an unrelated event.  

BTW, TM is no small hiccup:

Transverse myelitis is a serious condition involving inflammation of the spinal cord that can cause muscle weakness, paralysis, pain and bladder problems. In rare instances, vaccines have triggered cases of transverse myelitis; although it can also be caused by viral infections.

They state the vaccine known as AZD1222 — uses an adenovirus that carries a gene for one of the proteins in SARS-CoV-2, the virus that causes Covid-19. The adenovirus is designed to induce the immune system to generate a protective response against SARS-2. The platform has not been used in an approved vaccine, but has been tested in experimental vaccines.

Please read:  https://madisonarealymesupportgroup.com/2020/09/02/covid19-pcr-a-test-that-tells-you-your-body-is-the-enemy-a-vaccine-would-be-death-by-1000-cuts/

Excerpt:  

However, this protocol exists in all human DNA and exactly corresponds to C8. Therefore, what the PCR test is doing is equating C8 (which is present in ALL human DNA) as a foreign hostile material and indeed the coronavirus – Covid19 – itself.

IT FOLLOWS THAT ANY EFFICIENT COVID19 VACCINE MUST SERVE TO EITHER DELETE C8 (AS THE CORONAVIRUS), OR SUBSTANTIALLY SUPPRESS IT. HOWEVER, DOING BOTH, OR EITHER, WILL CERTAINLY RESULT IN THE DEATH, OR SEVERE MENTAL AND PHYSICAL IMPAIRMENT OF THOSE WHO TAKE IT.

https://madisonarealymesupportgroup.com/2020/08/24/gsk-whistleblower-covid-vaccine-caused-sterility-in-97-of-women/   BTW: this has happened to thousands of women in India already:  https://madisonarealymesupportgroup.com/2020/08/27/scrubbed-from-internet-history-of-gates-foundation-sterilizing-hundreds-of-thousands-of-young-girls-in-india-with-hpv-vaccine-must-see-video/

https://madisonarealymesupportgroup.com/2020/08/12/what-is-life-like-for-the-vaccine-injured/

https://madisonarealymesupportgroup.com/2020/09/06/interview-science-vs-the-vaccine-religion/?

https://madisonarealymesupportgroup.com/2018/06/21/u-s-government-continues-to-pay-millions-in-vaccine-injuries-death-settlements/

 

Vaccine Trial Halted After Participant Became Ill

https://www.cbsnews.com/news/covid-19-vaccine-trial-astrazenca-oxford-dr-fauci/

AstraZeneca halting COVID-19 vaccine trial is “one of the safety valves,” Dr. Fauci says

The halting of AstraZeneca’s coronavirus vaccine trial is “not uncommon,” Dr. Anthony Fauci, the nation’s top infectious disease expert, said Wednesday. Being alert for potential adverse reactions is part of the process, he explained.

“It’s really one of the safety valves that you have on clinical trials such as this,” he said on “CBS This Morning.” “So it’s unfortunate that it happened. Hopefully they’ll work it out and be able to proceed along with the remainder of the trial.”

AstraZeneca paused its Phase 3 trial on Tuesday after one participant became ill. It was not clear what symptoms the participant had. AstraZeneca is one of three companies currently in the final phase of vaccine trials. (See link for article)

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$200 Million Paid Out in 2020 For Vaccine Injuries and Deaths

https://healthimpactnews.com/2020/september-doj-report-lists-200-vaccine-injuries-and-1-vaccine-death-compensated-during-6-month-period-and-thats-without-a-fast-tracked-covid-vaccine/

by Brian Shilhavy
Editor, Health Impact News

The federal government Advisory Commission on Childhood Vaccines (ACCV) under the U.S. Department of Health and Human Services met on September 4, 2020, and the Department of Justice reported that during a 6-month period from February 16th through August 15th this year, 200 vaccine injuries and one death were compensated through the National Vaccine Injury Compensation Program (NVICP).

You can read the full report here.

So far in 2020 the NVICP has paid out $200 MILLION in damages due to vaccine injuries and deaths. (Source.)

These damages were caused primarily by the annual flu vaccine, and other childhood vaccines that have gone through the FDA approval process.

What will these numbers look like after the COVID vaccines are fast-tracked?

(See link for article)

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UN Admits Gates-Funded Vaccine is Causing Polio Outbreak in Africa

Sept. 4, 2020

By News Wire

https://21stcenturywire.com/2020/09/04/un-forced-to-admit-gates-funded-vaccine-is-causing-polio-outbreak-in-africa/

The United Nations has been forced to admit that a major international vaccine initiative is actually causing a deadly outbreak of the very disease it was supposed to wipe-out.

While international organisations like the World Health Organization (WHO) will regularly boast about ‘eradicating polio’ with vaccines—the opposite seems to be the case, with vaccines causing the deaths of scores of young people living in Africa.

Health officials have now admitted that their plan to stop ‘wild’ polio is backfiring, as scores children are being paralyzed by a deadly strain of the pathogen derived from a live vaccine – causing a virulent wave of polio to spread.

Officials now fear this new dangerous strain could soon ‘jump continents,’ causing further deadly outbreaks around the world.

Currently, the first experimental COVID-19 vaccine is being tested on the African population through GAVI Vaccine Alliance, another organization funded by the Gates Foundation. A large round of human trials is taking place in South Africa, run by the University of the Witwatersr and in Johannesburg—another Gates-funded institution.

This latest revelation from Africa should prompt journalists and health advocates to ask harder questions about the efficacy and safety of the much-hype COVID ‘miracle’ vaccine.

(See link for article)

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**Comment**

Vaccines are not without risks, and the experimental COVID-19 vaccine is bypassing standard safety protocols in an effort to speed up the process.  Another way to speed this process up is for the FDA to give it “emergency use authorization” (EUA).  If you are concerned about this potential, please contact your representatives and alert them to the inherent dangers in this.  Also, alert them to the fact that those who are immunocompromised with other conditions, such as Lyme/MSIDS are at even greater risk of vaccine injury.  Getting a vaccine should be a personal choice – not mandated.

For more:  https://madisonarealymesupportgroup.com/2020/05/30/say-no-to-forced-covid-19-vaccination-sign-petition/

ICAN has also started an Emergency Petition to halt numerous clinical trials unless ALL adverse reactions are tracked:  https://madisonarealymesupportgroup.com/2020/08/28/emergency-petitions-to-halt-numerous-clinical-trials-of-covid-19-vaccine-unless-all-adverse-reactions-are-tracked/

https://madisonarealymesupportgroup.com/2020/07/09/81-of-clinical-trial-volunteers-suffer-reactions-to-cansino-biologics-covid-19-vaccine-that-uses-hek293-human-fetal-cell-lines/

And once again, there are conflicts of interest all over the place:  https://madisonarealymesupportgroup.com/2020/07/08/new-docs-nih-owns-half-of-moderna-vaccine/

Interview: Science vs. The Vaccine Religion

https://www.jeremyrhammond.com/2020/09/01/interview-science-vs-the-vaccine-religion  (Interview in link)

by Sep 1, 2020

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On August 20, I was interviewed by Nate the Voluntaryist for his podcast about the topic of vaccines. I discussed how the science differs from dogmatic proclamations we are constantly inundated with by adherents to what I call the “vaccine religion”. Here are notes on topics we covered:

  • Origin of vaccine skepticism
  • False claim vaccine-autism hypothesis started with 1998 Lancet study
  • What the government and media say science says vs. what the science says
  • Clarifying a misunderstanding about Bill Gates’ depopulation agenda
  • Vaccines not studied for long-term effects including mortality prelicensure
  • DTP vaccine associated with increased rate of childhood mortality, a “non-specific effect” (NSE)
  • Prelicensure studies criminally inadequate
  • Synergistic effects and absence of studies into long-term effects of vaccinating according to the CDC’s schedule
  • Non-live vaccines generally associated with increased childhood mortality
  • Toxicity of ingredients, i.e., aluminum and mercury
  • Opportunity costs of vaccination
  • Measles vaccine associated with beneficial NSEs, but measles infection is also associated with lower mortality and a decreased risk of much more serious diseases later in life including cancer and cardiovascular disease
  • Getting flu shot can increase risk of illness
  • Population level effects, e.g., how measles vaccine has shifted the risk burden in the event of exposure onto those at higher risk
  • The claim that “vaccines safe and effective” is meaningless; an individual risk-benefit analysis is required
  • Mandates are gross violation of the right to informed consent
  • We’re all indoctrinated into a propaganda version of history, a reflection of the “vaccine religion”; but 90% of decline in infectious disease mortality occurred before there were vaccines that could possibly help explain it
  • How the Leicester method helped eradicate smallpox
  • What is needed are randomized controlled trials comparing health outcomes between vaccinated and unvaccinated children; observational studies are prone to selection bias
  • The problem of “healthy user bias”, e.g., in studies on flu shots and elderly mortality and a 2015 MMR-autism study
  • Vaccine-conferred vs natural herd immunity
  • The idea that science is “settled” and of a “consensus” on vaccines is delusional
  • There’s no serious discussion about vaccines in the mainstream discourse; every article always follows the same script
  • John Walker-Smith, coauthor with Wakefield on the 1998 Lancet study, appealed and was reinstated
  • Media and government do policy advocacy not education and journalism; they never address legitimate concerns but instead falsely caricature dissenters and critics as not having any
  • Elimination of exemptions and even medical exemptions in California; Richard Pan views doctors as not practicing medicine but performing an administrative function for the state
  • US children are chronically ill, and the idea that a product specifically designed to alter the functioning of the immune system and that children receive upwards of 72 doses of by the age of 18 has nothing to do with this is ludicrous
  • To determine causality, you have to do the science, which they refuse to do
  • Overturning of scientific “consensus” is called scientific advancement!
  • Bill Maher clip on chronic illness; the need for a paradigm shift away from drugs as solution to health problems; the influence of pharma on the practice of medicine
  • The Vaccine Injury Compensation Program and legal immunity for vaccine manufacturers; the elimination of the key incentive to develop safer and more effective means of disease prevention
  • The need for a paradigm shift
  • Where are all the studies into why a small proportion of children died from measles to develop targeted interventions rather than implementing a one-size-fits all, indiscriminate mass vaccination policy?
  • Why doesn’t the CDC recommend maintaining vitamin D sufficiency during winter to prevent severe flu?
  • Why do some people get infected with SARS-CoV-2 and not get COVID-19? Why is the focus entirely on developing a vaccine, which is the endgame of lockdown measures?
  • Lockdown measures violate fundamental rights; individuals need to be able to assess their own risks
  • Lockdown advocates are narrowly focused on preventing COVID-19 deaths, refusing to consider harms from the measures; the need to assess harms in terms of quality adjusted years of life lost
  • Lockdown measures prevent low-risk people from getting on with their lives and developing herd immunity
  • Sweden’s success and failure; lockdown measures, too, failed to protect those at highest risk in nursing homes
  • Irrational use of masks, e.g., running alone outdoors in a mask; universal masking not evidence-based; shortcomings of mask studies
  • Prolonged close contact required for transmission to occur; irrational fear of passing someone in a supermarket aisle, hiking outdoors, etc.
  • For those under 65 and healthy, the risk of severe COVID-19 is negligible
  • School closures don’t make sense; policies based on fear not data; lack of consideration for harms and weighing risks rather than futilely trying to eliminate risk
  • New York ordered nursing homes to accept COVID-19 discharged from hospitals
  • Liberty is the answer; e.g., government deciding what businesses are “non-essential” is Orwellian
  • We can prevent as many deaths as possible without destroying the economy and doing more harm than good
  • Jim Jordan vs Fauci clip on racial justice protests and Fauci’s inconsistency and hypocrisy in saying people “can draw your own conclusion” when it comes to joining crowds of protests and insisting he won’t express opinion on limiting people’s freedoms while having advocated lockdown measures including business closures due to risk of transmission
  • How Fauci was instrumental in persuading policymakers to implement lockdowns with his deceptive claim that SARS-CoV-2 is ten times deadlier than influenza
  • William Thompson, CDC whistleblower, on how they manipulated data to conceal an increased risk of autism; how that whole episode is dismissed as a “conspiracy theory” despite him being on tape admitting to having done so
  • How even advocating informed consent is now being equated as “anti-vaccine”, which is in turn falsely equated with “misinformation”
  • Censors direct social media users to the CDC, but the CDC lies, which can be shown by looking at its own sources, e.g., “Vaccines Do Not Cause Autism” page
  • CDC vaccine advisory committee corruption, e.g., Paul Offit
  • CDC and FDA serve the industry not public health
  • The medical establishment has utterly and abysmally failed with disease prevention and is itself a leading cause of death
  • Doctors are limited in their practice by the system; my personal experience with leaky gut and how the one good doctor I had retired because “I can’t practice medicine”
  • Our experience getting kicked out of a dental clinic for declining fluoride treatment and my confrontation with the dentist
  • The need to do one’s own research
  • How we learned to stop listening to doctors and trust our own judgment
  • Bill Maher vs. Bill Frist clip on 2009 swine flu vaccine; Maher correctly notes it wasn’t a very serious flu; Frist expresses faith in vaccines and falsely claims flu shots are 98% effective; Frist says we should look at the science while telling pregnant women to get the pandemic flu vaccine, which studies later associated with an increased risk of miscarriage; studies associated flu shots with increased risk of that pandemic strain
  • The CDC’s fear marketing strategy
  • Media’s false characterizations of the 1998 Lancet study; Wakefield never credited for pioneering research in to relationship between gut disorders and autism
  • How media lie about why parents don’t vaccinate and how to immunize yourself against vaccine propaganda

Emergency Petitions to Halt Numerous Clinical Trials of COVID-19 Vaccine Unless ALL Adverse Reactions Are Tracked

The NIH and Moderna have rigged the clinical trial of their COVID-19 vaccine, mRNA-1273, to avoid capturing adverse reactions that occur more than 28 days after injecting this experimental vaccine. ICAN’s legal team has filed an emergency petition to stop this unethical conduct.
ICAN previously filed a petition to the FDA demanding that this clinical trial include a placebo. The clinical trial for this vaccine was then delayed and when its design was finally issued, it included a placebo. But it appears that NIH and Moderna have decided to play a different game to avoid capturing safety issues that could prevent licensure of their mRNA-1273 vaccine. 
Their trick is to only capture adverse reactions that occur more than 28 days after injection if the participant withdraws from the clinical trial. This is nonsensical, since there is little for a participant to withdraw from after getting two doses during the first 28 days of the clinical trial. Once a participant has received both doses, if anything, a participant would have an incentive to remain part of the follow-up check-ups to address any adverse effects.
There could be many autoimmune, neurological and chronic health disorders which have a major impact on the quality of life that this experimental vaccine could cause. All of which may only arise more than 28 days after the injection. But yet, as long as the participant does not withdraw from the clinical trial, these will nonsensically be ignored as if they did not occur. This is unethical and renders vacuous any claim of safety for this product based on this trial.
Given that efficiency in this trial will be tracked for two years, the only reason to not track safety for this same duration is to avoid detecting safety issues that would prevent licensure.
ICAN’s legal team, headed by Aaron Siri, has therefore filed a citizen petition and an emergency stay petition demanding that the clinical trial design for this vaccine be updated to require that all adverse reactions for the entire period of the clinical trial be tracked. These petitions also demand that the number of participants in this trial be increased and that they be tested before and after injection for any T-cells to SARS-CoV-2. ICAN intends to take further legal action if its rational and sensible requests are not met.
Pfizer and BioNTech have also rigged the clinical trial of their COVID-19 vaccine, BNT162b, to avoid capturing many potential life-altering adverse reactions that may occur from this experimental vaccine. ICAN’s legal team again filed an emergency petition to stop this unethical conduct.
While Pfizer and BioNTech have now included a placebo control group in their clinical trial, these companies have decided to play a different game to avoid capturing safety issues that could prevent licensure of their COVID-19 vaccine, BNT162b.
The study design for the clinical trial for BNT162b provides that — despite reviewing efficacy for at least 2 years — it will only capture “adverse events” for 1 month and “serious adverse events” for only 6 months after each dose.
The adverse events captured beyond a month after injection should not be limited to “serious adverse events,” since there are many autoimmune, neurological, and chronic health disorders which have a major impact on the quality of life, yet are categorized by the FDA as “adverse reactions” and not categorized as “serious adverse reactions.” To wit, there are a myriad of post-licensure adverse reactions reported by consumers and physicians and are also listed in the package inserts for one or more vaccines that any individual living with would categorize as “serious”; yet the FDA, under its current guidelines, may not. These include, but are not limited to: alopecia, autoimmune disease, lupus erythematosus, vasculitis, Bell’s Palsy, hypotonia, migraine, myelitis, neuropathy, seizures, mental disorders, rhinitis, and vertigo. 
The study design for BNT162b nonetheless provides that these adverse events should be captured for only 1 month after vaccination while “serious adverse events” are captured for 6 months. These artificial limitations are unethical and make any claim of safety for this product based on this trial specious at best.
Incredibly, the efficiency of Pfizer and BioNTech’s vaccine in this trial will be tracked for two years. As such, the only reason to not track safety for this same duration is to avoid detecting any safety issues that would prevent licensure. If BNT162b causes a systemic autoimmune issue to arise two months after vaccination, it would be irresponsible and unethical not to capture that reaction just because an autoimmune issue falls into the artificially defined zone of being an “adverse event” or “non-serious adverse event,” rather than what the FDA has decided to label a “serious adverse event.”
ICAN’s legal team filed a citizen petition and an emergency stay petition demanding that the clinical trial design for this vaccine be updated to require that all adverse reactions for the entire period of the clinical trial be tracked. These petitions also demand that the number of participants in this trial be increased and that they be tested before and after injection for any T-cells to SARS-CoV-2. ICAN intends to take further legal action if its rational and sensible requests are not met.
AstraZeneca and the University of Oxford have also rigged the clinical trial of their COVID-19 vaccine, ChAdox1 nCoV-19, to avoid capturing many potential life-altering adverse reactions that may occur from this experimental vaccine. ICAN’s legal team once again filed an emergency petition to stop this unethical conduct.
Unlike the clinical trials for Moderna and Pfizer’s vaccines for COVID-19, which are occurring in the United States, the current clinical trial for AstraZeneca’s COVID-19 vaccine is not under the direct authority of the FDA, since this clinical trial is not occurring in the United States.  
News reports have indicated that AstraZeneca will be starting a new clinical trial in the United States for its COVID-19 vaccine that presumably will include a placebo control group. In the meantime, its current clinical trial occurring outside the United States persists in using a MenACWY vaccine as a control. As if that were not enough to rig this trial’s safety results, the study design for their vaccine, ChAdox1 nCoV-19, like the design of Pfizer’s vaccine, provides that, despite reviewing efficacy for at least 2 years, it will only capture “adverse events” for 1 month and “serious adverse events” for only 6 months after each dose. 
Therefore, ICAN’s legal team has also filed a citizen petition and an emergency stay petition demanding that the clinical trial design for this vaccine be updated to require that all adverse reactions for the entire period of the clinical trial be tracked against a placebo control group. These petitions also demand that the number of participants in this trial be increased and that they be tested before and after injection for any T-cells to SARS-CoV-2. ICAN intends to take further legal action if its rational and sensible requests are not met.
Just as the pharmaceutical companies will never rest when it comes to promoting and selling their vaccine products, we will never rest in exposing the truth regarding these products.  
Stand for vaccine truth and help us keep winning! Help us start 2020 strong. Donate $50, $100, $500, or $1000 today!

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**Comment**

Ponder this:

All of a sudden, after decades of over the counter use in travelers, being on the WHO’s List of Essential Medicines (the safest and most effective drugs needed in a health system), and being used by billions of people for autoimmune issues like Lupus, HCQ is supposedly dangerous. Yet, an experimental – never used before COVID-19 vaccine that’s bypassing the normal 5-19 year observation period, that manufacturers insist upon and have been granted indemnification by public officials, doesn’t use a true placebo and will only track adverse reactions that occur more than 28 days after injection if the participant withdraws from the clinical trial, is acceptable.

Anyone else see a problem here?

This is scientific hypocrisy at work reminiscent of the Lyme debacle:  https://madisonarealymesupportgroup.com/2020/04/26/cdc-playbook-learning-from-lyme/