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Abstract
Gastrointestinal (GI) adverse events are the most common limitation of glucagon-like peptide-1 receptor agonists and dual glucose-dependent insulinotropic polypeptide/glucagon-like peptide-1 receptor agonists.
- GLP-1 receptor agonists and dual GIP/GLP-1 receptor agonists are significant advancements in treating type 2 diabetes and obesity.
- GI adverse events frequently lead to discontinuation of these therapies.
- The prevalence of GI issues suggests a need for better management strategies for patients using these treatments.
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