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

Only 13% of oncology trial press releases from major pharma companies include precise data — raising concerns about ...

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

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

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

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 ...

While both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have released guidance on the ...

On the heels of similar moves in France and the European Union, U.S. health authorities are calling for a pause in the use of ...

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