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Carol Taccetta, MD, FCAP

A Drug Safety Physician’s Correspondence with the FDA: A Quest for Accuracy in Investigational Bivalent mRNA COVID-19 ‘Vaccine’ Adverse Event Reporting

Introduction   On November 4, 2022, the Centers for Disease Control and Prevention (CDC) and U.S. Food and Drug Administration (FDA) concluded that, based on Vaccine Adverse Events Reporting System (VAERS) and v-safe data received between August 31, 2022, and October 23, 2022, “Health care providers and patients can be […]