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Adverse Reactions

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FDA Panel Rejects Deramiocel Cardiac Claim After Lancet Publishes HOPE‑3 Results

A 9–3 advisory vote and critical FDA reviews increase doubt about final approval ahead of the August 22 PDUFA date.

Manufacturer Recalls Generic Zyrtec Over Possible Ranitidine Contamination

FDA Approves Decnupaz for Rare Blood Cancer

FDA Launches First Real-Time Clinical Trial Pilot With AstraZeneca and Amgen

Viatris Recalls One Lot of Xanax XR Nationwide After Tablets Fail FDA Dissolution Test

FDA Approves Filspari to Reduce Proteinuria in FSGS Patients Without Nephrotic Syndrome

Soleno Faces Securities Class Action Over DCCR Safety as Investors Weigh May 5 Lead‑Plaintiff Deadline

Lilly Urges Recall After Finding New Impurity in Compounded Tirzepatide With B12

TG Therapeutics Lifts 2026 Outlook After Strong Briumvi Year, Shares Jump

FDA Approves Aqvesme for Thalassemia Anemia, First U.S. Therapy for Both Patient Groups

MediNatura Recalls ReBoost Nasal Spray Lot Over Mold and Bacterial Contamination

FDA Approves Moderna’s mNEXSPIKE for Seniors and High-Risk Adults as CDC Drops Recommendations for Healthy Children and Pregnant Women