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Psychiatric Adverse Events and Administration Challenges Associated with GLP-1 Receptor Agonists for Weight Loss: A
Ali Hindi1, Mohamed Mekkawy2, Hala Shokr1
1Division of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester M13 9PL, UK.
Glucagon-like peptide-1 receptor agonists like semaglutide are linked to psychiatric risks, while tirzepatide shows higher injection site reactions and misuse. Liraglutide appears to have a lower risk profile for weight management.
Area of Science:
- Pharmacovigilance
- Clinical Pharmacology
- Public Health
Background:
- Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are widely used for weight loss.
- Concerns exist regarding adverse events beyond common gastrointestinal, renal, and pancreatic effects.
- Understanding these risks is crucial for safe clinical practice and policy.
Purpose of the Study:
- To investigate psychiatric risks, administration-related adverse events, and misuse of semaglutide, liraglutide, and tirzepatide for weight management.
- To analyze real-world adverse event data to identify safety signals.
Main Methods:
- Disproportionality analysis using proportional reporting ratios (PRR) and reporting odds ratios (ROR).
- Utilized the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database.
- Excluded gastrointestinal, renal, and pancreatic adverse events to focus on other risks.
Main Results:
- Semaglutide showed significant disproportionality for psychiatric events: anxiety, depression, and suicidal ideation.
- Tirzepatide had higher signals for injection-site reactions and inappropriate use (incorrect dosing, off-label administration).
- Liraglutide exhibited a comparatively lower risk profile.
Conclusions:
- Semaglutide is disproportionately linked to psychiatric adverse events in real-world weight management.
- Tirzepatide is associated with increased injection-site complications and misuse.
- Liraglutide presents a lower risk profile, highlighting the need for monitoring, education, and regulatory oversight for GLP-1 RAs.
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