The U.S. Food and Drug Administration on Tuesday released a 10,000-page cache of documents pertaining to the Emergency Use Authorization (EUA) of the Pfizer-BioNTech COVID vaccine.

The documents provide more insights into the FDA’s process for approving the vaccine, and may also shed more light on the safety and efficacy of the vaccines and the number and nature of adverse effects that were observed during the clinical trials and the first months after the EUA was issued.

The documents were made public as part of a court-ordered release schedule stemming from an expedited Freedom of Information Act (FOIA) request by Public Health and Medical Professionals for Transparency (PHMPT).

PHMPT, a group of medical and public health professionals and scientists from Harvard, Yale, UCLA and other institutions, submitted the request in August 2021.

The FOIA request asked for the approximately 400,000 pages of documents pertaining to the approval of the Pfizer COVID vaccine to be made public, including safety and effectiveness data, adverse reaction reports and a list of the vaccine’s active and inactive ingredients.

When the FDA ignored the request, PHMPT sued the agency in September 2021, taking the case to the U.S. District Court for the Northern District of Texas. On Feb. 2, federal judge Mark Pittman issued an order requiring the FDA to release redacted versions of the documents in question according to the following disclosure schedule:

However, the FDA released smaller sets of documents in November and December 2021 and January 2022, while the legal case was ongoing.

The first batch of documents, produced in November 2021 and totaling a mere 500 pages, revealed safety concerns and the fact that more than 1,200 vaccine-related deaths occurred within the first 90 days following the release of the Pfizer-BioNTech COVID vaccine.

The documents also revealed a nine-page list of adverse events observed during that same period. The list recently was circulated widely on social media and wrongly attributed to the set of documents released March 1.

https://childrenshealthdefense.org/d...ine-documents/

Other documentation pertains to “the standard, nearly $2.9 million user fee payment to FDA from Pfizer” and to “the confidential nonclinical overview for the vaccine,” Brennan said.

Brennan noted some documents included in the cache, such as the fast track designation letter and Pfizer’s request for a waiver from adding a suffix to the vaccine’s name, are “not typically released” to the public.

I thought we were going to need to wait 40+ years for things to be declassified or just released in general to know the real numbers. This could get interesting.

I haven't heard the word Covid on the news all week. Its over

If anything substantial is found in these documents, that’ll be the left’s new talking point…‘it’s over guys…what difference does it make?’

What else do you do besides post about COVID on a forum? Srs

If only there was stuff out there from legit medical experts & journalists to inform us that drug companies are pos who cover up & manipulate trial data, tell lies etc to make vast sums of money & that the chance to jab the entire world was too good to resist & maybe you shouldn't get their jabs & boosters rushed to market in just months injected in you & be a mass clinical test subject.

3 million bucks to approve one fake vax (not counting all the others - including one's being pulled). nice business model for the FDA. pzifer and all the other drug companies keeping the FDA open with those dollars

Sacklers just had to pay up another 6Billion