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TEVA's Prolia Biosimilar Gets FDA Nod, Xolair Filing Accepted
Teva wins FDA approval for Prolia biosimilar Ponlimsi and secures Xolair biosimilar filing review by the FDA and EMA, strengthening its biosimilars push.
FDA Says Amgen’s Tavneos Linked to Liver Injuries, Deaths
The FDA said it has identified 76 cases of drug-induced liver injuries with reasonable evidence of being causally linked to Tavneos.
FDA Warns Of Fatal Liver Risks Linked To Amgen Tavneos Use
FDA flags liver injury risk tied to Amgen Tavneos, citing drug-induced liver injury and rare vanishing bile duct syndrome complications.
April Dogs Of The Dow: One To Buy
April 2026 Dogs of the Dow update: Verizon is the only âdividend dogcatcherâ stock. Read the full list here.
https://www.fda.gov/drugs/fda-adverse-event-monitoring-system-aems/october-december-2025-new-safety-information-or-potential-signals-serious-risks-identified-fda
Sentiment scored by an AI model on article tone. Not investment advice.
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