FDA is Now Saying It Will Take 75 Years to Produce Clinical Data on Pfizer’s COVID-19 Vaccine

The Food and Drug Administration (FDA) is now saying that it will take 75 years, rather than their initial estimate of 55 years, to produce clinical data to the public on Pfizer’s COVID-19 vaccine.

The FDA is telling a court of law that they discovered 59,000 more pages of the clinical data that it will have to produce to the public. They now claim they can analyze more than 500 pages per month, but the additional pages will add two decades to the initial estimate of time it will take to produce the documents.

“If you find what you are reading difficult to believe—that is because it is dystopian for the government to give Pfizer billions, mandate Americans to take its product, prohibit Americans from suing for harms, but yet refuse to let Americans see the data underlying its licensure,” said Aaron Siri, an attorney who is working on the case.

The Public Health and Medical Professionals for Transparency brought on the case, demanding that the FDA provide the information to the public in a timely manner. This group includes Peter Doshi, an associate professor at the University of Maryland School of Pharmacy; Dr. Carole Browner, a research professor at the University of California–Los Angeles’s David Geffen School of Medicine; and Dr. Harvey Risch, a professor of epidemiology at the Yale School of Public Health.

“The entire purpose of FOIA is government transparency. In multiple recent cases, in upholding the FOIA’s requirement to ‘make the records promptly available,’ courts have required agencies, including the FDA, to produce 10,000 or more pages per month, and those cases did not involve a request nearly this important–i.e., the data underlying licensure of a liability-free product that the federal government requires nearly all Americans to receive,” Siri said.

“As the present pandemic rages on, independent review of these documents by outside scientists is urgently needed to assist with addressing the shortcomings and issues with the response to the pandemic to date,” he added.

Big League Politics has reported on the whistleblowers who have emerged to expose Pfizer for shuttering discussion of the chopped up fetal parts used to produce the COVID-19 vaccine:

In the latest shocking revelation from Project Veritas, a Pfizer whistleblower has come forward to explain how the company attempted to stop the public from realizing their COVID-19 vaccines may have been synthesized from the mutilated tissue of aborted fetuses.

Pfizer manufacturing quality auditor Melissa Strickler came forward to Veritas to explain how the company tried to suppress this information to bolster their profits during the COVID-19 pandemic. She shared their corporate public relations strategy to keep dissent to a minimum.

Her testimony can be seen here:

“They’re being so deceptive in their emails, it’s almost like it is in the final vaccine. It just made me not trust it,” Strickler said.

“I have no one else to turn to when my own company won’t be honest with me. What I was told to do was to trust Project Veritas and to go with you guys by lawmakers, by lawyers,” she added.

She shared emails to Veritas from Pfizer Senior Director of Worldwide Research Vanessa Gelman and Pfizer Chief Scientific Officer Philip Dormitzer explaining how fetal tissue could have been used to synthesize vaccines and how that this information should be suppressed by the Big Pharma giant.”

Big Pharma and the government officials in their pocket have much to hide about these experimental COVID-19 vaccines synthesized at warp speed. This is why they are refusing to produce the documents.

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