Risk of Suicide, Hair Loss, and Aspiration with GLP1-Receptor Agonists and Other Diabetic Agents: A Real-World Pharmacovigilance Study.

Aspiration FAERS GLP-1 receptor agonist Hair loss Pharmacovigilance Suicidality

Journal

Cardiovascular drugs and therapy
ISSN: 1573-7241
Titre abrégé: Cardiovasc Drugs Ther
Pays: United States
ID NLM: 8712220

Informations de publication

Date de publication:
12 Sep 2024
Historique:
accepted: 28 07 2024
medline: 12 9 2024
pubmed: 12 9 2024
entrez: 12 9 2024
Statut: aheadofprint

Résumé

With the increasing popularity of glucagon-like peptide 1 receptor agonists (GLP1-RAs), numerous safety concerns arose pertaining to suicide, hair loss, and aspiration risks. We attempted to validate these concerns. We queried four pharmacovigilance databases to compare GLP1-RAs to sodium-glucose transporter 2 inhibitors (SGLT2is) with respect to these adverse events (AE): the FDA Adverse Event Reporting System (FAERS), the Australian Database of Adverse Event Notifications (DAEN), the European Medicines Agency's (EudraVigilance), and the World Health Organization-Vigibase. OpenVigil 2.1 was utilized to perform a disproportionality analysis for GLP1-RAs, SGLT2is, dipeptidyl peptidase 4 inhibitors (DPP4is), sulfonylureas, metformin, and insulin. The following indices were extracted from the FAERS database from Q4/2003 until Q3/2023: relative reporting ratio (RRR), proportional reporting ratio (PRR), reporting odds ratio (ROR), and chi-squared (χ No positive signals were observed between GLP1-RAs and either suicide, hair loss, or aspiration risks. Semaglutide [ROR = 0.60 (0.51-0.71)] and liraglutide [ROR = 0.28 (0.23-0.35)] had higher suicidal events than DPP4is and SGLT2is. GLP1-RAs were the most reported class with hair loss [ROR = 0.61 (0.60-0.64)], and semaglutide, liraglutide, and dulaglutide were the three leading medications. GLP1-RAs ranked lower with aspiration events, which were led by sitagliptin and DPP4is as a group. GLP1-RAs exhibit higher reporting of suicide, hair loss, and aspiration events when compared to several other antidiabetic medications despite not meeting the criteria for positive signals yet. This warrants intensive monitoring and reporting.

Identifiants

pubmed: 39264502
doi: 10.1007/s10557-024-07613-w
pii: 10.1007/s10557-024-07613-w
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Michael Nakhla (M)

Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA, USA. Michael.Nakhla@StVincentHospital.com.

Ambica Nair (A)

Department of Internal Medicine, Ocean University Medical Center, Brick, NJ, USA.

Prachi Balani (P)

Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA, USA.

Aditi Ujjawal (A)

Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA, USA.

Pramukh Arun Kumar (P)

Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA, USA.

Mahati Dasari (M)

Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA, USA.

Zeynep Yukselen (Z)

Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA, USA.

Kannu Bansal (K)

Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA, USA.

Sarju Ganatra (S)

Division of Cardiovascular Medicine, Department of Medicine, Lahey Hospital and Medical Center, Burlington, MA, USA.

Sourbha S Dani (SS)

Division of Cardiovascular Medicine, Department of Medicine, Lahey Hospital and Medical Center, Burlington, MA, USA.

Classifications MeSH