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Discontinuation before conception, guided by each drugs pharmacokinetic profile, remains prudent to minimize potential fetal exposure: approximately 35 days for semaglutide (t 7 days), 2535 days for tirzepatide (t 5 days), and 3 days for liraglutide (t 13 h)

The clinical evidence base for semaglutide as an active pharmaceutical ingredient applies to the studied FDA-approved formulations, not directly to compounded versions

Selected entries are chosen based on the type of product and the potential safety impact of the recall or warning

"Increases in GLP-1RA dispensing were greatest for females, highlighting the importance of educating patients and prescribers on sex-specific safety risks [eg, concerns during pregnancy]," the team noted

Theyre typically mild and temporary, often resolving as doses are gradually increased

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