Now, as a follow up to that report, DailyClout reveals that Jeyanthi Kunadhasan, MD, part of that same Research Team, found even more damning evidence showing that Pfizer delayed recording deaths in Case Report Forms (CRFs), which allowed the company to not report those deaths as part of its emergency use authorization (EUA) data filing with the Food and Drug Administration (FDA). Daniel Perrier from the Research Team and Dr. Kunadhasan found, analyzed, and verified the data supporting this discovery. It is very likely that had the deaths been recorded when Pfizer became aware of them and then accurately filed as part of the EUA dataset, the public would not have accepted an EUA had been granted by the FDA.

On December 10, 2020, one day before the FDA granted Pfizer’s EUA, Susan Wollersheim, M.D. of the FDA/Center for Biologics Evaluation and Research (CBER) Office of Vaccines Research and Review, Division of Vaccines and Related Products Applications, presented, “FDA Review of Efficacy and Safety of Pfizer-BioNTech COVID-19 Vaccine Emergency Use Authorization Request” at the CBER Vaccines and Related Biological Products Advisory Committee 162nd Meeting. On page 42 of the slide deck, Dr. Wollersheim presented:

Posted in

Iron Will

Leave a Comment

You must be logged in to post a comment.