https://amgreatness.com/2022/04/08/doctor-crashes-fda-meeting-and-shares-the-whistleblower-story-they-ignored/
A doctor “crashed” a Food and Drug Administration’s meeting with outside vaccine experts earlier this week, to share a whistleblower’s story about the data integrity issues that plagued one of Pfizer’s clinical trials.
In September of 2020, a researcher from an organization testing Pfizer’s vaccine at several sites in Texas, emailed a complaint to the FDA, informing the agency of the company’s dangerously shoddy research practices. The FDA took no action on her email, and Pfizer continues to use the company.
Last week, the FDA authorized a second round of booster shots for people 50 and older and for those with certain immunocompromising conditions.
The Vaccines and Related Biological Products Advisory Committee (VRBPAC) met in an open session on April 6 to discuss “considerations for use of COVID-19 vaccine booster doses and the process for COVID-19 vaccine strain selection to address current and emerging variants.”
Dr. Peter Doshi, an assistant professor of pharmaceutical health services at the University of Maryland, and an associate editor at The British Medical Journal (BMJ), took the opportunity to tell the whistleblower, Brook Jackson’s, story.
In the fall of 2020, Jackson was the regional director for the Ventavia Research Group, the company that was conducting Pfizer’s pivotal phase III trial in Texas. She told the BMJ last November that she witnessed researchers falsifying data, unblinding trial participants, and employing inadequately trained vaccinators. She also said researchers were slow to follow up on adverse events.
Jackson has submitted her evidence to a federal court.
During an interview with the Blaze’s Daniel Horowitz in February, the whistleblower said Pfizer’s clinical trials were so riddled with fraud and abuse of the scientific process there was zero credibility left.