POLITICS

Liberals Rejoice Irrationally as FDA Approves Pfizer Vaccine Despite Poor Results; FDA Skips Key Clinical Trials and Advisory Committee Review

The FDA announced on Monday that the Pfizer-BioNTech COVID-19 vaccine has been licensed for the prevention of the disease in those aged 16 and up, but the timing of the announcement raises concerns.

Liberal media hacks ecstatically shared the news they’d been waiting for since Trump left office, when the vaccination miraculously morphed into humanity’s only hope.

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“It’s mandate time!” They yelled in some form or another as they frantically plotted how they might now demand that conservatives be held down as a needle was shoved in their arm.

What’s more, it arrived precisely in time for booster shots!

But hold on for a second.

These same bootlickers were singing an entirely different tune when Trump was in charge just a few months ago. They raised concerns about the vaccine being hurried and shortcuts being cut in order to get it out faster.

Now that Biden is in office fraudulently, they are following along like sheep, while the FDA refuses to conduct critical clinical trials and dismisses accumulating evidence that the vaccine is less efficient than natural immunity.

Perhaps they should have adhered to their guns, but liberals prefer mindless obedience.

Even the mRNA technology’s creator is speaking out against their hasty decision.

 

According to a report published in JAMA, the Journal of the American Medical Association, therapies are now subjected to significantly less examination and clinical trials than in the past, with the majority passing after just being evaluated on one control group.

This has allowed the FDA to speed forward the approval of the Pfizer vaccine, despite the fact that it has had disastrous outcomes, with vaccinated people spreading the infection as much as – if not more than – those who have recovered spontaneously.

Even the CDC had to make a U-turn and confess it.

Surprisingly, the FDA also delegated to the producer the task of conducting essential vaccine trials on some of the most vulnerable demographics, such as pregnant women. Several mandatory studies that should have been completed before full approval are still pending, and it will be up to Pfizer to see that they are completed and the results are reported.

As a result, we have determined that you must conduct the following investigations based on appropriate scientific data:…


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

…10. Organization of Teratology Information Specialists (OTIS)/MotherToBaby Pregnancy Registry study C4591022, titled “Pfizer-BioNTech COVID-19 Vaccine Exposure During Pregnancy: A Non-Interventional Post-Approval Safety Study of Pregnancy and Infant Outcomes.” The deadline for submitting the final protocol is July 1, 2021.

To put it another way, Big Pharma now has complete control over the outcome of important clinical trials that will decide the efficacy of their own product, as well as the capacity to disguise results that could expose them to liability or discourage people from taking their vaccine.

The FDA’s failure to perform its duties did not end there. They never completed an advisory c in addition to all the other processes that were neglected.

In remarks to The BMJ, Kim Witczak, a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee, questioned the decision to award full permission so soon, and argued that the meetings are vital for public transparency and data scrutiny.

“These public meetings are critical in establishing trust and confidence, especially since the vaccines were released under emergency use authorisation at breakneck speed.

The public is entitled to a transparent process, especially as the demand for boosts and mandates grows.

It’s already alarming that full approval is based on only six months’ worth of data, despite two-year clinical studies. Pfizer supplied the product to placebo individuals before the studies were done, so there is no control group.”

Diana Zuckerman, president of the National Center for Health Research, also chastised the lack of transparency.

“It’s clear that the FDA isn’t interested in hearing from anyone else. However, making decisions behind closed doors can increase reluctance. It’s critical to have a public conversation about the types of data available and their limits. We need to know when weighing risk versus benefit.” Zukerm –

The decision to completely approve the Pfizer vaccine is simply the latest alarming move made by US health officials who have been misleading or blatantly wrong since the outbreak began. They’ve also been keeping critical information from the public the entire time it’s been coming out.

In other words, the fact that a corrupt agency in Biden’s administration has signed off on whatever these radicals are trying to do is useless Because these hacks have zero credibility.

tRuSt ThE sCiEnCe. Ever onsider your options?

You may read the entire permission letter here:

 

 

Source
www.thegatewaypundit.com www.fda.gov www.thegatewaypundit.com

Margaret Taylor

Experienced communications professional with 10 years of experience in international journalism.

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