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Waiting for FDA approval The most conservative approach is simply waiting

The most frequent adverse events are gastrointestinal side effects that are mild to moderate, dose-dependent, and transient during the first weeks of treatment

Comparative safety data shows acute kidney injury was listed in 0.47% of tirzepatide adverse event reports versus 1.07% of semaglutide reports in the FDA Adverse Event Reporting System (FAERS), with the reporting odds ratio favoring tirzepatide

High-protein foods help maintain muscle mass and support recovery, especially if patients are consuming fewer calories