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and to reduce/stop if uncontrolled hyperkalemia or to control uremic symptoms when GFR 30 ml/min per 1.73 m2 and subsequently decline to an eGFR 30 ml/min/1.73m2

Post-marketing surveillance and FDA Adverse Event Reporting System (FAERS) data have documented isolated reports of patients experiencing dyspnea while taking GLP-1 medications, but establishing causality remains challenging

Injection site reactions Redness, swelling, or itching at the injection site

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Body changes: Track your body weight, changes in appetite or cravings, any episodes of nausea or vomiting, and your calorie intake