Paul Offit: It ‘Felt Like the Fix Was In’ Before FDA Panel Voted to Reformulate COVID Booster Shots

Paul Offit: It ‘Felt Like the Fix Was In’ Before FDA Panel Voted to Reformulate COVID Booster Shots
Dr Paul Hoffit By Karl Withakay/ CC-BY-SA-4.0
Megan Redshaw
By Megan Redshaw, J.D.
Updated:
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One of the members of the U.S. Food and Drug Administration’s (FDA) vaccine advisory panel explained why he voted against adding an Omicron component to fall COVID-19 booster shots raising serious questions over a lack of critical data and the Biden administration’s role in politicizing the process.
In a July 6 interview with ZDoggMD, Dr. Paul Offit, director of the Vaccine Education Center and professor of pediatrics in the Division of Infectious Diseases at Children’s Hospital of Philadelphia, described the Vaccines and Related Biological Products Advisory Committee’s (VRBPAC) recent meeting as “unusual.”
Megan Redshaw
Megan Redshaw
J.D.
Megan Redshaw is an attorney and investigative journalist with a background in political science. She is also a traditional naturopath with additional certifications in nutrition and exercise science.
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