In an amended reply to the FDA’s rejection of his concerns about Pfizer’s clinical trials, Dr. Sin Hang Lee says the FDA is glossing over potential risks of an mRNA vaccine while concealing its true efficacy.
By: Children’s Health Defense Team
Pfizer’s announcement in November 2020 that clinical trials showed its COVID-19 vaccine was “95% effective” prompted Dr. Sin Hang Lee, a Connecticut pathologist, to question Pfizer’s methodology and petition the U.S. Food and Drug Administration (FDA) to require accurate counts of COVID-19 cases in the Pfizer/BioNTech COVID-19 mRNA vaccine trial before granting the vaccine Emergency Use Authorization (EAU).
“Until an accurate count of COVID-19 cases in the vaccinated and placebo groups has been determined for vaccine efficacy evaluation, we are asking the FDA to stay its decision regarding the emergency use authorization for this vaccine.”
Here’s the sequence of events as they unfolded: