What Does MEDWATCH Stand For?

MEDWATCH stands for FDA Safety Information And Adverse Event Reporting Program

MEDWATCH, or the FDA Safety Information and Adverse Event Reporting Program, is a resource established by the U.S. Food and Drug Administration (FDA) to facilitate the reporting and monitoring of adverse events, product defects, and other safety concerns related to pharmaceutical drugs, biologics, medical devices, and dietary supplements. The program empowers healthcare professionals and the public to report safety information, which assists in the identification of potential risks and enhances the overall safety and efficacy of medical products. Through MEDWATCH, the FDA aims to promote patient safety, improve healthcare outcomes, and ensure timely communication of vital safety information.