The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it ...

The U.S. Food and Drug Administration has started "real-time reporting of adverse event data," according to an annoucement ...

Adverse medical events are a major source of global morbidity and mortality, occurring in 10 percent of hospitalizations, according to a meta-study published in the British Medical Journal of ...

The U.S. Food and Drug Administration (USFDA) has suspended the biologics license of Ixchiq (Chikungunya Vaccine, Live), ...

Hospitals in New Jersey saved $641 million by reducing the number of adverse medical events in the state by 77,342 from 2012 through 2016, according to a report released by the New Jersey Hospital ...

The agency shared information from reports by users of compounded semaglutide and tirzepatide who have experienced health ...

From August 19, 2025, the FDA announced that B. Braun Medical Inc. (B. Braun) is voluntarily recalling 2 lots of its Lactated ...

Dr. Chris Longhurst, chief medical and digital officer at UC San Diego Health, told Ruth he sees a lot of potential in Emmie, ...

These events led to more trial withdrawals due to adverse events (RR 3.07, 95% CI 1.73-5.43), and serious adverse events were more common with medical cannabinoids than among controls (RR 1.81, 95 ...

AIIMS Bhopal functions as a Medical Devices Adverse Event Reporting Monitoring Centre (MDMCs) and also as a Regional Training ...