by Leo Hohmann, Leo Hohmann:
Pharmaceutical giant Pfizer tested its Covid “boosters” on fewer than two dozen people before Joe Biden’s Food and Drug Administration approved the mRNA shots for full public use, explosive new documents reveal.
The watchdog group Judicial Watch obtained documents through a Freedom of Information Act lawsuit which forced the government to turn over the information.
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The organization has published the first batch of those documents and they expose Pfizer’s lax 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.
The FDA said it based its decision to approve the shots on the documents presented by Pfizer, as well as input from the CDC, the Israeli Ministry of Health and the University of Bristol in the UK.
Based on those paltry numbers of just 23 human guinea pigs and then checking in with the Israelis and a single British university, the FDA gave its rubber stamp and a total of 8.9 million people across America were injected with Covid boosters within three weeks.
Judicial Watch released 58 pages of records from the FDA showing that a Pfizer “study” administered the shots to 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 refused to respond to an August 2021 Freedom of Information Act (FOIA) request. (Judicial Watch Inc. v. U.S. Department of Health and Human Services (No. 1:22-cv-00730).
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-19 vaccine. 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).
These documents are just the latest confirmation of Robert F. Kennedy Jr.’s statement about the safety of “vaccines.” None of them are put through the sort of rigorous, double-blind placebo-controlled testing protocols that other medicines are required to go through. And we know that, even with these rigorous testing protocols, there are many examples of medicines that slip through and end up injuring and killing people, forcing companies to pull them from the market.
