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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

Consolidated cases will now be a part of MDL 3094 In Re: Glucagon-Like Peptide-1 Receptor Agonists (GLP-1 RAS) Products Liability Litigation in the Eastern District of Pennsylvania before the Hon

If any occur, discontinue the medication and contact your veterinarian

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The PlexusDx Precision Peptide Genetic Test examines 14 pathways and 150+ genetic insights, including GLP1R and MC4R variants that influence digestive sensitivity

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