Did You Know? Thousands of Adverse Events Since Pfizer mRNA Vaccine Rollout

November 3, 2022 • by Dr. Chris Flowers, MD, MBBS, FRCR, FSBI
Video by Dr. Chris Flowers

The data in this video is from Pfizer’s “post marketing” document, which is titled, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021.”

The analysis in Pfizer’s post marketing document was completed on February 28, 2021. Its appendix shows 1290 Adverse Events of Special Interest (AESIs). An “adverse event” is also known as a “side effect.” Additionally, within just two and a half months after its COVID-19 vaccine received Emergency Use Authorization (EUA) approval, Pfizer documented:

Therefore, Pfizer was aware of tens of thousands of adverse events, many severe, from its mRNA COVID vaccine by the end of February 2021.

Pfizer submitted its post marketing analysis to the U.S. Food and Drug Administration (FDA) on April 30, 2021. So, four and a half months after granting Pfizer’s vaccine EUA, the FDA knew about the tens of thousands of adverse events.

Yet, rather than informing the public and pausing the use of this drug to do further studies, both Pfizer and the FDA remained silent about the incredible harms resulting from it. Moreover, they – along with the Centers for Disease Control and Prevention (CDC), public health agencies, governments, media, and the majority of medical professionals – continued to aggressively push, and even mandate, for people to receive this harmful shot.

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Associate Professor of Radiology (retired), University of South Florida. Previously Associate Professor of Radiology and Biomedical Imaging, University of California, San Francisco. Retired academic cancer radiologist, author and scientific paper reviewer for multiple radiology journals.

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This content was originally published here.