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Report Adverse Events: Patients can submit adverse event reports to the FDA through the MedWatch program

FDA Approves Higher-exposure level parenteral-route administration Semaglutide [PMID: 41931277] Laboratory literature summary: FDA Approves Higher-exposure level parenteral-route administration Semaglutide

The most commonly reported side effects include: Nausea and vomiting Diarrhoea or constipation Stomach pain and bloating Dizziness Headache or fatigue Low blood sugar (more likely in people with type 2 diabetes, especially when Wegovy is taken with other diabetes medication) Acid reflux and heartburn Insulin resistance Symptoms tend to vary from person to person, and most should settle as your body gets used to the medication

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And the answers are no, no, and no, said Alice Yuk-Yan Cheng, MD, an associate professor of medicine at University of Toronto, during a presentation on the retatrutide trial results at an American Diabetes Association meeting on June 6