FDA Requests to Defer Pfizer-BioNTech Data until 2076
On November 15th, 2021 the U.S. Food and Drug Administration (FDA) requested that the federal court defer the release of Pfizer-BioNTech’s coronavirus concoction documents until 2076. That is fifty-fives years from today. Why does the FDA want to suppress medical data?
The FDA, vouching for the major pharmaceutical company, requested1 that a federal judge defer the total release of over 329,000 Pfizer-BioNTech documents, to allowing stalling the distribution, to an agreement of just 500 pages per month, until the year 2076. That rate would equal 54.83, (fifty-five) years before Americans know the entire truth behind the concoction being mandated into the arms of all Americans.
Could there be an alternate reason behind the FDA requesting the delay of these documents? While the experimental coronavirus vaccines are considered “safe”, how much long term data do we have on the efficacy of these injections? How much research has been done into the mass injection of synthetic nanoparticles in the population? While Pfizer says to “trust the science”, does current world data show that the coronavirus boosters are necessary for everyone, and if so, should these boosters be mandated?
Freedom of Information Act
New York attorney, Aaron Siri, wrote on his substack2,
“[I]n August and immediately following approval of the vaccine, more than 30 academics, professors, and scientists from this country’s most prestigious universities requested the data and information submitted to the FDA by Pfizer to license its COVID-19 vaccine.”
Adding, “The FDA’s response? It produced nothing. So, in September, my firm filed a lawsuit against the FDA on behalf of this group to demand this information.” Aaron Siri continued, “To date, almost three months after it licensed Pfizer’s vaccine, the FDA still has not released a single page. Not one.”
The lawsuit reads:
“The entire purpose of the Freedom of Information Act (FOIA) is to assure government transparency.” read a filing a complaint regarding the request to attain information from the major pharmaceutical company via the FOIA. It continued, “It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated in over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.”
“It took the FDA precisely 108 days from when Pfizer started producing the records for licensure on May 7, 2021, to when the product was licensed on August 23, 2021. We assume, as the FDA has stated, that it conducted an intense, robust, thorough and complete review and analysis of those documents in order to assure that the Pfizer Vaccine was safe and effective for licensure. The FDA now has an equally important task of making those documents available to the Plaintiff in this case and the public at large in at least the same timeframe.”
This isn’t the first time the FDA has evaded public transparency.
Conclusion
What information or data is the FDA trying to suppress, and why did they suggest 55 years? By that time many of the initial patients will have died from old age, and by that time, those who survived will be forced to overlook whatever data is unveiled as Big Pharma attempts to bypass the Freedom of Information Act by trickling information piece by piece, as they continue to rack up big profits, extending the demand by inventing “new and improved” concoctions, deemed “boosters.” If these boosters are mandated, so should the distribution of the information to those who participate in their mass mRNA coronavirus ‘vaccine’ experiment.
https://www.sirillp.com/wp-content/uploads/2021/11/020-Second-Joint-Status-Report-8989f1fed17e2d919391d8df1978006e.pdf
https://aaronsiri.substack.com