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- FDA Identifies Cases of Serious Liver Injury in Patients Taking Tavneos (avacopan) for Severe Active Anti-Neutrophil Cytoplasmic Autoantibody Associated Vasculitis
- Aphreseller Issues Voluntary Recall of Kian Pee Wan Capsules Due the Presence of Undeclared Dexamethasone and Cyproheptadine
- Amneal Issues Recall of Magnesium Sulfate in Water for Injection, USP 4 g/100mL (NDC 70121-1720-3) Due to Product Mix-Up
- FDA Is Requiring Warning about Vitamin B6 Deficiency and Associated Seizures for Drug Products Containing Carbidopa/Levodopa
- Cardinal Health Issues Voluntary Nationwide Recall of Webcol™ Large Alcohol Prep Pad