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However, in early January, District Judge Mark Pittman ordered them to deliver 55,000 pages per month.

Since that time the Public Health and Medical Professionals for Transparency has posted all of the Pfizer documents on its website with the most recent drop happening last June 1.

Pfizer’s classified document is titled “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-Feb-2021.” The document, which Pfizer tried to hide, was delivered to the FDA as part of the company’s biologics license application for its mRNA COVID-19 vaccine.

The document listed VAED and Vaccine-Associated Enhanced Respiratory Disease (VAERD) in a section titled “Important Potential Risk.”

Pfizer claimed in their confidential document that up to Feb 28, 2021, they had received 138 cases reporting 317 likely relevant events suggestive of VAED. Of these, 71 were medically significant resulting in eight disabilities, 13 serious events, and 38 of the 138 people died.

Of the 317 relevant events reported by 138 people, 135 were marked as “drug ineffective,” 53 as dyspnoea (struggling to breathe), 23 as COVID-19 pneumonia, eight as respiratory failure and seven as seizure.

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