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In some individuals, these excipients can provoke mild hypersensitivity reactions, manifesting as localised pruritus or erythema

Keep tirzepatide in its original packaging with pharmacy labels clearly visible, which helps identify the medication during security screening and provides dosing information if needed

henceforth referred to as an active supply. All patients were required to have at least two consecutive-months of GLP-1 RA active supply during the study period

Approximately 7% of participants in the Phase 2 clinical trial experienced skin sensitivity, compared to 1% in the placebo group

Research Status: Tirzepatide is widely studied with extensive Phase 3 data (SURMOUNT trials)