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In 2014, the FDA issued a safety alert for this drug after the New England Journal of Medicine linked it to a 27 percent increased risk of heart failure

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Active Ingredient Semaglutide (Introductory GLP-1 Agonist) Total Strength per Vial Calibrated for 0.25mg and 0.5mg initial delivery Dose Classification Starter Phase & Early Titration Step 1 Primary Manufacturer Glenmark Pharmaceuticals Ltd Therapeutic Class Incretin Mimetic / Antidiabetic / Anti-Obesity Administration Route Subcutaneous Injection (Weekly calibrated dose) Supply Format 1 Multi-dose Vial / Pen System

Initially registered on April 19, 2022, it has never been inspected by the FDA