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Clinical studies on Semaglutide and breastfeeding are limited, necessitating further studies to understand its potential risks and long-term effects comprehensively

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The adverse reactions, excluding hypoglycemia, reported regardless of investigator assessment of causality in 5% of patients treated with JANUVIA 100 mg daily and more commonly than in patients treated with placebo, are shown in Table 1 for the clinical trials of at least 18 weeks duration

Baseline renal and hepatic assessment before starting, regular lipase monitoring because of pancreatitis risk associated with tirzepatide, and standardised follow-up appointments