PHMPT send FOI request to FDA for all registration files

A Freedom of Information (FOI) request was sent to FDA by the lawyers of the non-profit group called Public Health and Medical Professionals for Transparency (PHMPT), to obtain all data and information use by FDA to grant registration of Pfizer’s Comernity on August 23, 2021. [1]

PHMPT exists for the sole purpose of disseminating to the public the data and information in the biological product files for each of the COVID-19 vaccines, to allow independent experts to conduct their own review and analyses, starting with Pfizer.

Initial document released of post-marketing data collected by Pfizer from volunteer reports, in the first 90 days after the EUA reveals they were well aware in Feb. 2021 that 1,223 deaths and more than 42,000 reports totaling 139,888 adverse reactions post jab, and yet despite this warning data the FDA “has consistently maintained that the mRNA vaccine(s) are “safe and effective.”” [2]

The FDA has requested up to 75 years to fully release the data (see Dec 31, 2021 below).

Yet post-vaccine adverse reactions, for all COVID-19 vaccines keep piling up, including from clinical trial participants. [3, 4, 5, 6, 7, 8]

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