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FDA Has Blood On It’s Hands After Pfizer Document Release Reveals A Plethora Of Trial Data Injuries, Deaths

Documents list 158,893 vaccine adverse events and yet FDA still authorized its use

Credit: Contx


The Food and Drug Administration (FDA) has released a 38 page record of Pfizer COVID-19 adverse vaccine events, which Pfizer tried to keep secret until the year 2097. The release came after a successful Freedom of Information Request against the FDA became court ordered.

The 38 page document labelled “Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-FEB-2021” written by Worldwide Safety and Pfizer, focuses specifically on adverse reactions from the Pfizer – BioNTech COVID-19 mRNA vaccine.

“The FDA shall produce the remaining documents at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete,” the court said in their ruling.

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