Comirnaty got FDA approval, not the current deadly Covid-19 injection that will continue to be used almost exclusively.
There appears to be a lot of confusion about the approval of the covid-19 “vaccine” by the U.S. Food and Drug Administration (FDA) on Aug. 23, 2021.
While many mainstream media outlets quickly ran with the story that Pfizer’s existing mRNA injection was given the official green light from the FDA, supposedly making it easier to mandate, others are saying that the FDA issued approval specifically to BioNTech, a German vaccine corporation, for an injection that does not exist yet. (Watch videos below!)
The so-called approval is riddled with deceptions meant to trick the American public into thinking they have no choice but to take the jab, while at the same time protecting a major pharmaceutical company from legal liability. With the full authorization and licensure of Pfizer’s experimental series of mRNA inoculations, the Food and Drug Administration (FDA) just subverted their own federal regulations and gold standards, while ignoring the vast amount of injuries reported after inoculation.
Previously, BioNTech partnered with Pfizer to produce the current shot that is being administered under an emergency use authorization (EUA). However, this shot is technically a different shot than the “Comirnaty” shot referenced in the FDA’s recent approval announcement. The FDA acknowledges that Pfizer has “insufficient stocks” of the newly licensed Comirnaty vaccine available but has “a significant amount” of the Pfizer-BioNTech COVID vaccine — produced under Emergency Use Authorization (EUA) — still available for use. In other words, only the Comirnaty shot of the future is approved, and only when they have met certain requirements (see letter) In addition, because the new Comirnaty does not enjoy any liability shield, people injured could potentially sue for damages. And because adults injured by the vaccine will be able to show that the manufacturer knew of the problems with the product, jury awards could be astronomical. Pfizer is therefore unlikely to allow any American to take a Comirnaty vaccine until it can somehow arrange immunity for this product.
The FDA’s acknowledgement in its approval letter that there are insufficient stocks of the licensed Comirnaty, but an abundant supply of the EUA Pfizer BioNTech jab, exposes the “approval” as a cynical scheme to encourage businesses and schools to impose illegal jab mandates.
The press reported that vaccine mandates are now legal for military, healthcare workers, college students and employees in many industries. New York City Mayor Bill de Blasio has now required the vaccine for all teachers and school staff. The Pentagon is proceeding with its mandate for all military service members.
What was actually given full approval was a separate Pfizer-BioNtech vaccine product which goes by the name Comirnaty, which is not even currently available.
The FDA is violating multiple principles of medical ethics and is complicit in crimes against humanity after approving Pfizer and BioNTech’s new drug, Comirnaty. For eight months, this so-called vaccine has ravaged the health of the nation, with 3,033 cases of myocarditis and pericarditis, of which 1,335 came directly from the Pfizer shot. A shocking 8,396 blood clotting disorders were reported, of which 3,586 reports were attributed to Pfizer.
This drug company is also responsible for 44 percent of the 126,905 reports of anaphylaxis and over 200 cases of Guillain-Barré Syndrome. Pfizer is also responsible for 1,300 cases of Bell’s palsy. Tens of thousands of people have been sent to the emergency room because of these injections, with over 17,000 permanently disabled and over 13,000 pronounced dead after taking the shots. This holocaust is happening in the young and old, as the spike proteins congregate in vital organs and cause inflammation in the cardiovascular system.
All this pain and suffering will continue, and human immunity to coronaviruses will be permanently damaged because Pfizer’s “vaccine” protocol wanes within six months. For the past eight months, the FDA allowed an illegal emergency use authorization (EUA) to facilitate this holocaust. This EUA is illegal if there is an alternative treatment that is considered safe, effective and readily available. Millions of people have recovered using early anti-viral, immune-modulating treatments like ivermectin, hydroxychloroquine, zinc, vitamin D, etc., but the science has been suppressed. For 18 months, the FDA has refused to evaluate treatments that worked in the US and abroad, paving the way for destructive and illegally-authorized injections that have only added to the pain and suffering in the medical system.
Dr. Robert Malone, inventer of the mRNA technology on which the Covid vaccines are based, explains the chicanery the FDA is using to fool the American people.
Dr. Jane Ruby – FDA approval illegal! Pfizer insert proves criminal regulation violations
Former Senior HHS Trump COVID Advisor Dr. Paul Alexander addresses the deception of President Trump, led by the Pence Coronavirus Task Force, and how the FDA tricked the people.
Karen Kingston, former Pfizer employee, reveals how the FDA “approval” is sure to be the “checkmate” move to end the shots.
Source articles:
https://www.naturalnews.com/2021-08-26-fda-full-authorization-pfizer-vaccine-broke-the-law.html
https://www.naturalnews.com/2021-08-24-fda-approval-future-covid-vaccine-biontech.html
https://bit.ly/3zoXXej
https://bit.ly/3BkA7kn
