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- FDA Requires Safety Labeling Changes for Glucagon-Like Peptide-1 Receptor Agonists (GLP-1 RAs) Due to Potential Increased Risk of Rare But Serious Eye Condition
- FDA Investigating Serious Risk of Malignancy Linked to Zolgensma Gene Therapy
- Eugia US LLC Issues Recall of Vancomycin Hydrochloride for Injection USP 1.25g/Vial-30mL (Single Dose Vial) Due to Presence of Particulate Matter
- Counterfeit Versions of Eye Drops Found in Several States
- Par Health Issues Voluntary Nationwide Recall of Argatroban Injection Due to the Presence of Particulate Matter