The US Government regulator for drugs, the Food and Drug Administration, has just announced that it has voted full approval for the mRNA genetic vaccine of Pfizer and BioNTech, or did they? This supposed new status is being used by the Biden Administration and many states and companies to impose mandatory vaccinations. The notoriously conflicted Biden covid adviser, Tony Fauci of the NIAID, using that ruling, is calling for national mandatory vaccination for the country. What is not being revealed is the cesspool of corruption and conflicts of interest between the FDA and the major drug companies, including Pfizer, that stand behind the rushed approval. And it’s not full approval for Pfizer’s jab, only for BioNTech’s legally different vaccine. .
“…final stamp of approval”?
On August 23 as the FDA announced full approval for the Pfizer mRNA gene-edited substance. Or not quite, when the full papers of FDA are studied. Fauci, whose NIAID has financial interest in the vaccine, referred to the FDA decision as the “final stamp of approval.” It is however anything but final or an impartial, scientific rigorous medical evaluation. Rather it is a politically-motivated decision by an FDA that is corrupt beyond the imagination of most people.
Backtracking on its statement in 2020 that it would hold normal FDA advisory committee hearings with independent experts to discuss the Pfizer application for full approval, now the FDA told the British Medical Journal that they did not believe a meeting was necessary ahead of granting full approval of what is the most controversial vaccine in modern history. The BMJ quotes Kim Witczak, a drug safety advocate who serves as a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee, “These [FDA] public meetings are imperative in building trust and confidence especially when the vaccines came to market at lightning speed under emergency use authorization.”
Witczak continued with the alarming note, “It is already concerning that full approval is being based on 6 months’ worth of data despite the clinical trials designed for two years. There is no control group after Pfizer offered the product to placebo participants before the trials were completed.” Read that again, slowly. Pfizer tests destroyed their own control group mid-stream! And its six month rollout of the mRNA jab worldwide has resulted in catastrophic side effects which have been totally officially ignored. Is this “science” Dr Fauci?
The refusal of the FDA and its Acting Director, Janet Woodcock, to convene its Drugs Advisory Committee for discussion of the Pfizer and BioNTech decisions is even more shocking as in June three members of that same panel resigned in protest for being disregarded in another drug approval. NPR network reported, “Three experts have now resigned from a Food and Drug Administration advisory committee after the agency approved an Alzheimer’s drug called Aduhelm against the wishes of nearly every member on the panel.” One of the three, Dr. Aaron Kesselheim, in his resignation letter from the FDA Advisory Committee (June 10, 2021), wrote: “For both eteplirsen and aducanumab, the decisions by FDA administrators to ignore the Advisory Committee’s clear recommendations led to their approval of two highly problematic drugs that offered little evidence that they would meaningfully benefit patients…With eteplirsen, the AdComm (Advisory Committee) and FDA’s own scientific staff reported that there was no convincing evidence that the drug worked; both groups were overruled by FDA leadership… “
Now the FDA refusal to convene their advisory committee for the Pfizer decision is all the more astonishing in light of the fact that the Government Centers for Disease Control (CDC) in its official VAERS data bank for recording vaccine negative effects has recorded 8,508 reports of fatalities following the Pfizer mRNA shot in the past seven months, a number more than for all vaccines combined in the past 30 years. By denying a public hearing the FDA avoided any discussion of these alarming fatality numbers, let alone the tens of thousands of serious side-effects including heart attacks, blood clots, miscarriages, permanent paralysis following the Pfizer-BioNTech jabs. The public declaration by Fauci before approval that he expected it, is also unethical influencing, but that is the least of the crimes.
It seems the FDA executed a clever ruse in which it issued separate rulings for a Pfizer Inc.-BioNTech vaccine which is widely used in the USA, and another ruling for the similar vaccine of Pfizer’s German-based partner and developer of the mRNA platform, BioNTech of Mainz. It is only BioNTech that got FDA approval, but conditioned on completion of a series of further tests on select groups including infants, pregnant women and youth, by 2027. The US vaccine, Pfizer-BioNTech Covid-19 vaccine, only got extension of its Emergency Use Authorization (EUA), not full approval!
In their separate letter to Pfizer, the FDA stated, “…On August 23, 2021, having concluded that revising this EUA is appropriate to protect the public health or safety under section 564(g)(2) of the Act, FDA is reissuing the August 12, 2021 letter of (Emergency Use) authorization in its entirety with revisions incorporated to clarify that the EUA will remain in place for the Pfizer-BioNTech COVID-19 vaccine for the previously-authorized indication and uses…”(emphasis added).
Buried in a footnote in the letter the FDA admits there are two legally separate entities and vaccines—Pfizer-BioNTech Covid-19 Vaccine and BioNTech GmbH of Mainz with its own vaccine trade-named Comrinaty. The FDA writes that “The products are legally distinct with certain differences…” Legally distinct means two separate vaccines. If you find this confusing it is meant to be. Only under an EUA ruling is Pfizer presently exempt from vaccine liability. Some lawyers are calling the FDA ruse a classic “bait and switch” tactic, a form of fraud based on deception.
US vaccinologist and a developer of the mRNA technique, Dr Robert Malone, has accused the FDA of playing a “bureaucratic shell game” with their supposed early approval of the Pfizer Covid-19 vaccine. He cites the two separate FDA letters, “There is a letter for Pfizer and a letter for BioNTech. The New York Times and the Washington Post got it wrong. The authorization is not for Pfizer. The authorization is for BioNTech, and it will only be initiated at the time BioNTech product becomes available…”
Adding to the bizarre irregularities, in their two separate letters, one to BioNTech and another to Pfizer, the FDA repeatedly deletes the location of the vaccine manufacturing they approve. Why that? Is it in China where BioNTech has a joint agreement with Fosun Pharma of Shanghai to jointly produce and market Comirnaty vaccine for COVID-19? Why do they need to hide that location data from the public? Would it expose the entire fraud?