Cutting Corners: Liberals Mindlessly Rejoice as FDA Fully Approves Pfizer Vaccine Despite Poor Results; Skipped Key Clinical Trials and Advisory Committee Review … PLUS … [VIDEO]

GATEWAY PUNDIT | By Julian Conradson | August 23, 2021

On Monday, the FDA announced that it had approved the Pfizer-BioNTech COVID-19 vaccine for the prevention of the disease in individuals 16 years of age and older, but the rushed nature of their announcement raises questions.

Liberal media hacks rejoiced and gleefully spread the news they had been waiting forever since Trump left office and the vaccine magically transformed into their only hope for mankind.

“Time for mandates!” They exclaimed, in some form or another, as they feverishly began plotting how they could now call for conservatives to be held down while a needle gets jammed in their arm.

And how convenient, just in time for booster shots!

The tyrants in Biden’s regime also jumped at the news and immediately said they would force all active-duty military members to get the jab. They are expected to implement even more draconian restrictions now that the FDA has given the experimental and highly controversial mRNA vaccine their ‘blessing.’

FDA Approval of Pfizer Vaccine Sparks Wave of Mandates: Pentagon, New York City Public Schools Announce Requirements

Biden’s Surgeon General Vivek Murthy on Sunday said the FDA’s approval of the Pfizer vaccine will likely lead to more vaccine mandates. And that’s exactly what happened. Within minutes of the FDA’s approval of the Pfizer vaccine, the Pentagon and New York schools announced new requirements. The FDA on Monday granted a full approval to … Continue readingFDA Approval of Pfizer Vaccine Sparks Wave of Mandates: Pentagon, New York City Public Schools Announce Requirements

But wait just one second.

Just a few months ago when Trump was in charge, these same bootlickers were singing a completely different tune. They sounded the alarm about the vaccine being rushed and corners being cut so it could be distributed more quickly.

Now Biden fraudulently holds office and they follow along mindlessly like sheep as the FDA skips out on conducting crucial clinical trials and ignores mounting data that suggests the vaccine is less effective than natural immunity.

Perhaps they should have stuck to their guns, but mindless compliance is the liberal default.

Over the past few years the FDA has drastically changed the process to approve new drugs and biologics and have only accelerated since the China-virus was unleashed upon the world. New submissions for experimental treatments are being approved in record time, taking just months when they used to average over 3 years.

Even the inventor of the mRNA technology is speaking out against their rash decision.

According to a study by JAMA, the Journal of American Medical Association, treatments that get submitted for review are now subject to far less scrutiny and clinical trials than they have been in the past, with most now passing after being tested on just one control group.

This has enabled the agency to fast-track the passage of the Pfizer shot, despite awful results that have seen the vaccinated spread the virus as much – if not more – than those who have recovered naturally.

Even the CDC had to flip-flop again and admit as much.

CDC Finally Admits “Limited Evidence” Vaccine Provides Improved Protection for Those Previously Infected with COVID

Rep. Thomas Massie (R-KY) tweeted Saturday on a CDC study released on Friday. The study that found there is “limited evidence” to believe the COVID vaccine offers improved protection for those people who already had the disease. This is not a surprise. This is what doctors always believed before the days of the China Virus … Continue reading

Unbelievably, the FDA also turned over the responsibility to conduct necessary vaccine trials on some of the most important subgroups, like pregnant women, to the manufacturer. Several mandatory studies that should have taken place before full approval still need to be conducted and it will be up to Pfizer to ensure their completion and report the results.

Therefore, based on appropriate scientific data, we have determined that you are required to conduct the following studies:…

…4. Study C4591009, entitled “A Non-Interventional Post-Approval Safety Study of the Pfizer-BioNTech COVID-19 mRNA Vaccine in the United States,” to evaluate the occurrence of myocarditis and pericarditis following administration of COMIRNATY.

…10. Study C4591022, entitled “Pfizer-BioNTech COVID-19 Vaccine Exposure during Pregnancy: A Non-Interventional Post-Approval Safety Study of Pregnancy and Infant Outcomes in the Organization of Teratology Information Specialists (OTIS)/MotherToBaby Pregnancy Registry.” Final Protocol Submission: July 1, 2021

In other words, Big Pharma now controls the outcome of key clinical research that will determine the effectiveness of their own product and has the ability to obscure results that could hold them liable or discourage people from taking their jab.

The FDA’s dereliction of duty didn’t end with that. In addition to all the other steps that were skipped, they never completed an advisory committee review because they claim there were no “concerns or controversial issues,” despite an overwhelming number of cases with adverse side effects like myocarditis.

Kim Witczak, a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee, questioned the decision to grant full authorization so quickly, and said that the meetings are important for public transparency and to scrutinize any data, in comments she made to The BMJ.

“These public meetings are imperative in building trust and confidence especially when the vaccines came to market at lightening speed under emergency use authorization.

The public deserves a transparent process, especially as the call for boosters and mandates are rapidly increasing. These meetings offer a platform where questions can be raised, problems attacked, and data scrutinized in advance of an approval.

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.”

Kim Witczak, a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee, questioned the decision to grant full authorization so quickly, and said that the meetings are important for public transparency and to scrutinize any data, in comments she made to The BMJ.

“These public meetings are imperative in building trust and confidence especially when the vaccines came to market at lightening speed under emergency use authorization.

The public deserves a transparent process, especially as the call for boosters and mandates are rapidly increasing. These meetings offer a platform where questions can be raised, problems attacked, and data scrutinized in advance of an approval.

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.”

tRuSt ThE sCiEnCe.  Think for yourself.

The full approval letter can be found here:

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