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Abstract
Nausea or vomiting are common adverse events associated with glucagon-like peptide-1 receptor agonists, which may decline over time with continued use.
- Tolerance to nausea or vomiting may develop in patients receiving efpeglenatide.
- Longitudinal dynamics of these adverse events have not been quantitatively characterized until now.
- The study focuses on non-diabetic patients with obesity.
- Repeated time-to-event modeling is utilized to analyze efpeglenatide-induced nausea and vomiting.
- Findings could inform future dose-escalation strategies.
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