Avacopan shows a favorable safety profile in ANCA-associated vasculitis in real-world settings, with hepatobiliary events as ...

The US Food and Drug Administration (FDA) has announced that starting on 1 October 2026, manufacturers must submit adverse ...

Add Yahoo as a preferred source to see more of our stories on Google. The FDA announced it will now update its Adverse Event Reporting System every day, instead of once per quarter. Photo courtesy FDA ...

Improving Access to Cancer Clinical Trials for Patients From Culturally and Linguistically Diverse Backgrounds in Australia: A Survey of Clinical and Research Professionals Using a retrospective, ...

Epidemiologic factors and survival outcomes of patients with metastatic malignant melanoma. This is an ASCO Meeting Abstract from the 2025 ASCO Annual Meeting I. This abstract does not include a full ...

Most common gastrointestinal issues seen were nausea/vomiting, abdominal pain, and diarrhea. HealthDay News — The rate of emergency department visits for adverse events among patients dispensed ...

Nearly 25% of hospital admissions included at least one adverse event, as indicated from data from 2809 admissions at 11 hospitals. The 1991 Harvard Medical Practice Study (HMPS), which focused on ...

More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) within the deadline set by federal regulations, finds an analysis of recent ...

Results presented here showed simultaneous amputation with osseointegration yielded similar improvements in mobility and ...

Australia's pharmaceuticals watchdog is investigating a spike in adverse event reports for Vyvanse, the country's most commonly prescribed ADHD medication. The increase coincides with a leap in ...