Comirnaty Vaccine FDA Approval is Misleading

Comirnaty Vaccine Approval is Misleading

The mRNA vaccines use an entirely new scientific method.  It “is truly an experiment on the human race, because they did not do the kind of science that they should have done even to get Emergency Use Authorization.”

Dr. Peter McCullough, an epidemiologist and cardiologist points out that none of the injection trials have data safety monitoring boards; Standard safeguards were intentionally eliminated for the rapid rollout of these shots to eliminate any public outcry because the incriminating data is not being collected.  Doctor Robert Malone – inventor of the mRNA technology being used in the vaccines, shares his sentiments.

Had proper monitoring boards been in place, the vaccination campaign would have been stopped by late January 2021, because of the high number of suspicious deaths.  There’s also the possibility of these shots causing antibody dependent enhancement (ADE), which is a big concern for the future..

With aggressive efforts by government working with pharmaceutical corporations and other for-profit groups to mandate COVID-19 vaccines and partnering with Silicon Valley and corporate media to censor public conversations about risks.

FDA ‘Surprise’ Approval of the Pfizer COVID Shot

On August 23, 2021, the U.S. Food and Drug Administration granted full approval to the COVID-19 mRNA injection developed by Pfizer/BioNTech, sold under the brand name Comirnaty, for use in people aged 16 and older. It’s the fastest approval in history and is based on just six months worth of data from 44,060 people.

At the outset half of them were vaccinated and half received a placebo. But in the second week of December 2020, Pfizer unblinded the control group and 93% of controls switched to get the real injection instead of remaining in the control group for the remainder of the trial, which is slated to continue for another two years. IOW, there IS no control group left against which to compare side effects and effectiveness.

Kinda suspicious that Fauci’s wife works for the #NIH, the NIH gives the AOK to the #FDA

The FDA was supposed to hold a public meeting of the Vaccines and Related Biological Products Advisory Committee and allow for public and expert input before the first COVID-19 vaccine was formally licensed. The meeting should have taken place before approval because COVID-19 vaccines are the first to ever have been distributed to the US population under EUA. But this didn’t happen.

“In 2017, pharma paid 75% – or $905 million – of the FDA’s scientific review budgets for branded and generic drugs, compared to 27% in 1993.”  in other words: We’ve investigated ourselves and found we did nothing wrong.

quebec nursesOn August 31 Robert F. Kennedy Jr. joined the Children’s Health Defense (CHD) in suing the FDA and director Janet Woodcock for for these intentional missteps:

“CHD argues that the licensure was a classic ‘bait and switch,’ allowing Pfizer, the Biden administration, the U.S. military and employers to exhort people to take ‘licensed’ vaccines when in fact the vaccines available and being administered continued to be the Pfizer-BioNTech Emergency Use Authorization (EUA) vaccines”
… the FDA violated federal law when it simultaneously licensed Pfizer’s ‘Comirnaty’ vaccine and extended Pfizer’s EUA for its vaccine that has the ‘same formulation’ and that ‘can be used interchangeably”

Google: “largest criminal fine in US history” and the answer is Pfizer.

The law (21 U.S. Code § 360bbb-3-(3)) on ‘authorization for medical products for use in emergencies’ requires the EUA designation be used only when ‘there is no adequate, approved and available alternative to the product for diagnosing, preventing or treating such disease or condition.’

The lawsuit alleges once the FDA approved and licensed Pfizer’s Comirnaty vaccine, there was no further basis for the FDA to preserve the EUA status for the Pfizer-BioNTech vaccine that Pfizer acknowledges has the ‘same formulation’ and is ‘interchangeable.’”

ironic-vaccine-mandateTo receive Emergency Use Authorization from the FDA, vaccine makers had to show the vaccines were at minimum 50% effective at preventing serious symptoms of COVID-19 disease – by August the Pfizer vaccine was at 42% and plummeting.   They were not required to demonstrate that the shots prevent SARS-CoV-2 infection or that it prevents transmission of the virus. They’re always talking about prevention of hospitalization and death but that is not what people think happens when you get a vaccine. We have been carefully taught to believe that when we get vaccinated, we will not get infected and we won’t transmit that infection to other people.

On the CDC site it mentions quarantine camps that are able to detain citizens deemed to be a risk to the rest of society.

The US federal government could also invoke its authority over interstate commerce and prohibit unvaccinated people from flying from one state to another that way. There’s already legislation introduced in Congress proposing this.

Mismanagement or Intentional Obstruction ?
From the beginning, health authorities have beeincubation,period,viral,infectionn neglectful when it comes to the treatment of COVID-19. They’ve even actively prevented safe and effective treatments from being used. Doctor Barbara Loe Fisher describes her experience:

“I had covid in December (2019). I had severe symptoms lasting 10 weeks into the end of February of 2020. I was left with long-COVID that lasted 16 months until a functional medicine doctor who tested me found that the COVID had reactivated a Epstein-Barr infection which was in remission.”

She was prescribed a short course of ivermectin to which she had an immediate “significant reduction in my symptoms”, which included cardiac symptoms that had been diagnosed by a cardiologist. “My energy shot up after that ivermectin and I stopped sleeping most of the day. My cardiac symptoms were significantly reduced. It was like I got my life back.”  Yet the government has gone after doctors who have urged people to get vitamin D, vitamin C, zinc, ivermectin and other licensed drugs that have been used without issues for decades.

30% of health care workers and medical doctors are refusing the pfizer vaccine and that is startling considering they’re the ones who are treating covid patients.  In other countries emerging research suggests that health workers’ acceptance of COVID-19 vaccines has ranged from roughly 28% to 82%. Acceptance was lower among women, Black and Latinx, rural and politically conservative health workers.

vaccine ineffectiveness, leaky vaccines, as well as vaccine safety issues — these issues aren’t just relevant for COVID.

The ultimate “public health authority” is the World Health Organization, and the largest benefactor of it is Bill Gates,; he gives money to it via the Bill & Melinda Gates Foundation and GAVI.

This financial leverage gives Gates a disproportionate amount of power over public health globally and, which he used primarily to expand vaccine use. At the same time, Gates is also a major Big Tech player, the main enforcer of censorship.  Big Tech censorship of the discussion makes informed consent impossible.

2/3rds of Americans don’t want vaccine mandates. They do not want to be required to show a vaccine passport in order to participate in society, enter a restaurant or a store, hold a job or go to college.

In hearings in 1987, companies begged Congress to give them full liability protection and Congress wouldn’t do it. They only gave the doctors full liability protection.

Only months into the USA’s vaccine rollout, a quarter of American hospital workers were unvaccinated, (Department of Health and Human Services). In America’s largest hospitals 1 in 3 workers hadn’t received the shot.

In 1980 seven vaccines were given to children; Tetanus, the DPT shot, measles, mumps and rubella (MMR) and oral polio vaccine. That was it. That’s all the children got.”  In 2021 children receive 72 doses of 16 different vaccines by the age of 18. The catalyst for this change  vaccines in the early 1990s was the partial liability protection Congress gave vaccine manufacturers in 1986 under the National Childhood Vaccine Injury Act. 

After the National Childhood Vaccine Injury Act (NCVIA) was first passed doctors were still liable for medical malpractice. The companies were still liable for design defect but absolved of failure to warn. In December 1987, in the dead of the night, an amendment was added to an omnibus budget bill … that completely let all the doctors and vaccine providers off the hook in a civil court of law. In hearings in 1987, companies begged Congress to give them full liability protection and Congress wouldn’t do it. They only gave the doctors full liability protection. The only positive that resulted from those hearings is VAERS – a decentralized system of safety provisions reporting: informing, recording, reporting safety provisions, that parents, doctors, and the public can report to.

VAERS is the only national vaccine adverse event reporting system, and why we know today that more than half a million covid vaccine reactions have been reported by the public, by doctors.  Over 13,600 deaths following covid vaccination as of August 20, 2021, and more than 55,820 post-COVID shot hospitalizations have been reported to VAERS as of 3rd week of August 2021

 In 2011, the U.S. Supreme Court sided with Wyeth in a DTP vaccine injury case (Bruesewitz v Wyeth) the prosecutor argued the vaccine injury was the result of a design defect (failure to make a product safer). Wyeth could have made the DPT vaccine safer.  The Supreme Court majority claimed the legislative history was clear — that Congress intended that vaccine manufacturers should have no liability for FDA licensed and CDC recommended vaccines. This was in fact the complete opposite of what the legislative history shows. Two of the Supreme Court judges, Justices Ruth Bader Ginsberg and Sonia Sotomayor, wrote a lengthy dissent, stating that the legislative history does not show that Congress wanted to give the companies complete liability protection.

In 1980 there was a firewall between the pharmaceutical industry and government. They’re now one and the same, and Pharma calls the shots at the FDA, the NIH and the CDC. (pfizer lead board member in 2021 was the president and CEO of the FDA in 2019)

vaers,vaccine,data,adverse,reactions,complications,pfizer,moderna,vaccines,monthly,so,far,yearly,disabled,myocarditis,pericarditis,thrombosis,anaphylaxis,bells,palsy,miscarriages,heart,attack,Fauci himself, is responsible for having allocated probably over $1 trillion in federal funding to researchers, principal investigators that are intimately and ultimately tied to pharma, over the 37 years he’s presided as director of the NIAID. His budget for fiscal year 2021 alone is $6.5 billion. The patents they created generates royalties to them. It’s a nightmare dystopia of raping the public from the federal treasury.

Marc Pilcher, ‘Bridgerton’ Emmy winner, dies age 53 of Covid-19 – CNN Style Pilcher was “double vaccinated” and had no underlying health conditions. He took multiple Covid-19 tests and tested negative to make the trip to the US for the Emmy’s ceremony and back to the UK.

The entire mandatory vaccination system in this country has been built on the myth that if you get vaccinated, you cannot get infected and transmit the infection to other people; that you have vaccine-acquired immunity that is robust and contributes to herd immunity. The truth is that vaccine-acquired immunity is often very temporary and sometimes you don’t get it at all. And really, herd immunity is more based on natural immunity … So, the term ‘immunization’ really should never be used anymore.

So far, 21 U.S. states have passed legislation that restrict or prevent COVID vaccine mandates or COVID vaccine passports. Several state governors have also issued executive orders to the same effect.

<– She isn’t the first Pfizer whistleblower to accuse the company of deceptive practices.  Karen Kingston has also made startling revelations