INTRODUCTION “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162b2) Received Through 28-Feb-2021,” Pfizer’s post-marketing report, a required U.S. Food and Drug Administration (FDA) compliance document, is one of the ways in which the FDA assessed patients’ risks associated with Pfizer’s COVID-19 vaccine, BNT162b2. The data within the Pfizer’s 5.3.6 analysis are not […]
Drbeen Explains Pfizer Vaccine Side Effects of Special Interest document
Pfizer recently released the first set of court ordered documents to the public, this is part of the Freedom of Information Act Case with the FDA. One document in particular, which covers the Adverse Events of Special Interest (AESI), has garnered a lot of attention. In this video, Dr. Been reviews said document, explaining […]