Pharmaceutical giant Pfizer tested its Covid “boosters” on fewer than two dozen people before Democrat President Joe Biden’s Food and Drug Administration (FDA) approved the mRNA shots for full public use, explosive unsealed documents have revealed.
Political watchdog group Judicial Watch forced the unsealing of the documents through legal efforts.
The organization has now published a batch of those documents to expose Pfizer’s far-from-rigorous testing practices.
According to the documents, Pfizer only tested the safety and efficacy of its Covid vaccine booster on 23 people in 2021 before putting in a request with the FDA to approve the shots for nationwide public use.
Biden’s FDA immediately approved the Covid booster shot and pushed it out to the public at the end of September 2021.
“The participants included 11 people aged 18 to 55 and 12 people aged 65 to 85,” Judicial Watch reported.
“Of the younger group, there were nine females and two males; eight of whom were white, one was black and two were Asian.
“Of the older group, six were female, six were males, and all were white.”
8.9 million people across America were injected with Covid boosters within just three weeks of the FDA’s approval of the shots.
Judicial Watch released 58 pages of records from the FDA showing that a Pfizer study surveyed just 23 people in 2021 to gauge reactions to its “booster.”
The FDA indicated that this production of records “represents our complete response to your request; no additional productions are anticipated.”
The records were obtained in response to a March 2022 lawsuit filed after the Department of Health and Human Services (HHS) failed to respond to an August 2021 Freedom of Information Act (FOIA) request.
The request was for records “submitted by Pfizer and BioNTech to the FDA, including BARDA, relating to ‘booster’ vaccinations for the SARS-CoV-2 virus.”
Biomedical Advanced Research and Development Authority, BARDA, has been heavily involved with the development of the Covid shots.
According to its website:
The Biomedical Advanced Research and Development Authority (BARDA) provides an integrated, systematic approach to the development of the necessary vaccines, drugs, therapies, and diagnostic tools for public health medical emergencies such as chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks; pandemic influenza (PI), and emerging infectious diseases (EID).
Judicial Watch President Tom Fitton issued a statement warning the American people to carefully examine the documents before being pressured by the Biden admin to take the booster.
“With the planned push for new boosters by the Biden administration, the public would do well to examine these troubling documents about the shotgun approval of prior COVID boosters,” said Fitton.