A new study reveals a novel approach to mitigating tissue damage caused by Streptococcus pyogenes, the flesh-eating bacterium responsible for severe infections such as necrotizing fasciitis. The ...

Under federal law, device makers must submit adverse event reports they receive from patients to the FDA’s Manufacturer And User Facility Device Experience (MAUDE) database within 30 days, researchers ...

The unraveling of Marc and Alain Cohens' relationship with Dana-Farber — where Marc was also a trustee — has created possible legal problems for the hospital.

A new study published in Nature Communications reveals a novel approach to mitigating tissue damage caused by Streptococcus ...

Although most manufacturer reports of medical device adverse events are reported on time, a considerable proportion are submitted late.

Adults taking the novel once-daily oral pill for plaque psoriasis have significantly higher rates of clear or almost clear ...

The intervention involved removing both isolated cannabis use and limited prenatal care as indications for urine drug ...

But a California student group alleges that the state’s University of California system has systematically violated that ...

"A lot of people in medicine feel very threatened right now, and very apprehensive about what the future holds." -- Celeste ...

Providing long-acting (LA) antiretroviral therapy (ART) to breastfeeding women with HIV who face adherence challenges may be ...

Reports on medical device adverse events widely exceed FDA deadlines, according to a recent study published in the BMJ. Read ...