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Quantity shortfalls in research tirzepatide vials are common and well-documented
The FDA generally allows compounding with these while they are under review
Both subgroup analyses demonstrated non-significant differences in WL between the GLP-1RAs and placebo groups with (SMD = 0.44, 95% CI -0.37 to 1.26) and (SMD = 0.74, 95% CI -0.32 to 1.79), respectively (Fig
The most common adverse events were nausea, vomiting, diarrhoea and constipation
Both peptides degrade rapidly in solution
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