Lizzy Lawrence leads STAT’s coverage of the Food and Drug Administration. She was previously a medical devices reporter. You can reach Lizzy on Signal at lizzylaw.53. WASHINGTON — The Food and Drug ...
The U.S. Food and Drug Administration is now providing real-time, daily publication updates on adverse event data from its reporting system. In an effort to modernize and provide transparency on ...
Adverse Drug Event Reporting: The Roles of Consumers and Health-Care Professionals: Workshop Summary
Adverse reactions to prescription drugs (adverse drug events, or ADEs) are quite common and usually do little harm to patients. But in a small percentage of cases, they can have serious consequences ...
FDA launches new AI-powered system to track drug and vaccine side effects in real time, replacing outdated databases and ...
As Department of Health and Human Services (HHS) and FDA leadership continue to look for ways to boost transparency and reshape the U.S' healthcare infrastructure, the U.S. drug regulator has unveiled ...
CHICAGO -- Adverse event risks varied across biologics used by asthma patients, an analysis of data submitted to the FDA Adverse Event Reporting System (FAERS) showed. In comparing relative number of ...
WASHINGTON, March 18, 2026 /PRNewswire/ -- Adverse drug events (ADEs)--injuries caused by medications-- are estimated to rank among the leading causes of death in the United States and represent a ...
The FDA recently sent a warning letter to Novo Nordisk, raising concerns about the drug company failing to report adverse drug events. The letter, dated March 5, outlines the FDA’s observations at the ...
Pevnick, M.D., M.S.H.S., discusses medications and the risk of an adverse drug event among older people after they get discharged from the hospital. Adverse drug events are common in the days and ...
Indian Pharmacopoeia Commission regularly monitoring adverse events of weight-loss drugs ...
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