A new analysis of global pharmacovigilance data indicates that while reports of psychiatric distress are common among users ...

The U.S. Food and Drug Administration has delayed reviews of two drugs chosen for the Trump administration's new fast-track ...

Americans cannot rely on the Food & Drug Administration (FDA) to guarantee that medical devices are safe, and a recent Government Accountability ...

The FDA Adverse Event Reporting System (FAERS) contains reports from health care professionals, consumers, and manufacturers on adverse events, serious medication errors, and product quality ...

Fred Hutchinson Cancer Center-led investigators found that higher patient-reported fatigue before cancer treatment aligned ...

Please provide your email address to receive an email when new articles are posted on . The FDA said some people using compounded semaglutide have experienced adverse events tied to overdosing. Lack ...

Officials say government found 604 'adverse events' from dietary supplements. Sept. 23, 2008— -- Serious side effects from the use of food supplements resulted in 604 "adverse-event" reports — a ...

Harm and the potential for harm from medical care is pervasive and well-documented. Much of the safety literature has historically focused on physical harm, but the Agency for Healthcare Research and ...

To increase transparency, the agency is publishing data from the FDA Adverse Event Reporting System daily rather than quarterly. (HealthDay News) — The U.S. Food and Drug Administration is now ...