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PMID:31536259

Abstract We conducted a disproportionality analysis of the FDA Adverse Event Reporting System (FAERS) database (2005 Q22024 Q3) to evaluate neurological adverse events (NAEs) associated with six glucagon-like peptide-1 receptor agonists (GLP-1 RAs): exenatide, liraglutide, lixisenatide, dulaglutide, semaglutide, and tirzepatide

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It may be used in controlled research settings for comparative evaluation of receptor activity, ligand-receptor interaction, and related analytical studies

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Diabetes Care 2019;42:S90-S102