The Food and Drug Administration is charged with making sure products, including medicines, delivered to American consumers have been tested for safety.
And a Pfizer booster shot that delivered in 2021 purportedly to help consumers fight off the COVID-19 pandemic was.
On 23 people.
That stunner comes from Judicial Watch, which reported on its access to 58 pages of records from the FDA.
They revealed “a Pfizer study surveyed 23 people in 2021 to gauge reactions to its COVID vaccine booster before asking the FDA to approve it.”
The FDA document showed the company confirmed that “represents our complete response to your request; no additional productions are anticipated.”
Judicial Watch said it accessed records after a lawsuit filed last year when the Department of Health and Human Services, now run by the radically pro-abortion Xavier Becerra, declined to respond to a 2021 Freedom of Information Act request.
The request was for documentation concerning the approval of that booster.
Involved in the process were Pfizer, BioNTech, a German drug company, and BARDA, the Biomedical Advanced Research and Development Authority.
Those newly obtained records “include a July study titled ‘Phase 1 Booster Safety and Immunogenicity Data up to 1 Month Post-Dose 3 of BNT162b2 30 µg [micrograms] in Study C4591001’ [that] provided ‘preliminary safety and immunogenicity data’ for a group that had received two vaccine shots and, seven to nine months later, a third (booster) shot.”
Continued…
Approved ~ MJM
