Research highlights the potential risks of antiepileptic drugs during pregnancy, including teratogenicity and ...

The FDA and CDC recommended a pause for Ixchiq, a chikungunya vaccine, following reports of adverse events in recipients 60 ...

Thoughts of suicide was confirmed as a side effect of finasteride (Propecia, Proscar), a 5-alpha reductase inhibitor approved ...

Revisions to classification criteria ‘will ensure homogeneous trial populations’ with data-driven scoring, a standardized MRI ...

Some U.S. biotech companies are considering moving early-stage trials of new medicines outside the United States as worry ...

Greeks remain 'spectators' to pharmaceutical innovation. New medicines are frequently approved, but never reach patients.

Greeks remain 'spectators' to pharmaceutical innovation. New medicines are frequently approved, but never reach patients.

Adds nine additional countries to the Company’s ongoing pivotal Phase 3 trial; Authorization granted in all EU countries ...

A recent study reveals that the average duration of ADHD medication for children and adolescents is more than three years. However, reliable, controlled data on the safety of marketed ADHD medicines ...

The U.S. Food and Drug Administration (FDA) on Wednesday approved Merck & Co. Inc.’s (NYSE:MRK) Welireg (belzutifan) for ...

Shares of the biotech fell around 15% on news the FDA is not only taking longer to review the drug, but will assemble an ...