Ozempic tablets are now available; investigational ALS treatment gains FDA Fast Track status; positive results for aficamten ...

HealthDay News — As an investigation continues into a hantavirus outbreak that killed three passengers and sickened five on an ocean liner, the World Health Organization (WHO) says the odds of broader ...

A major amendment has prompted the FDA to extend its review of subcutaneous lecanemab as a starting dose for early Alzheimer disease.

Relative vaccine efficacy was 26.6 percent, which met the criteria for noninferiority, superiority, higher-level superiority.

Based on the current evidence, there is no consistent association between vaccines and serious or long-term health outcomes.

It’s also not clear that HHS has the regulatory authority to enforce its threat without going through a formal rulemaking process, lawyers and dietitians say.

Botulinum toxin may slightly reduce monthly migraine days but has higher discontinuation rates due to adverse events.

Bladder-intact disease-free survival was 60% 2 years posttreatment with pembrolizumab combined with gemcitabine-based chemoradiation.

Glucagon-like peptide-1 (GLP-1) receptor agonists may be a potential novel treatment for alcohol use disorder, according to a ...

This marks a shift from years of aggressive regulation against flavored vapes after the FDA rejected marketing approvals for more than 1 million flavored products.

Ensitrelvir is an investigational oral antiviral under FDA review for the prevention of COVID-19 following exposure to an infected individual. It is designed to suppress the replication of SARS-CoV-2 ...