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Subsequent studies also examining data from the FDA Adverse Event Reporting System (FDA AERS) reported an increase in reporting rates of PDAC cases in GLP-1RA users over a broader study period 33,34

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Zhang Y, Wang S, Zhou L

Stuve serves on the editorial boards of Therapeutic Advances in Neurological Disorders, Expert Review of Clinical Immunology, and he is a section editor for Current Treatment Options in Neurology, has served on data monitoring committees for Genentech-Roche, and Novartis without monetary compensation, has advised Octave Bioscience, Ipsen, and Cellarity, receives grant support from EMD Serono, is a 2021 recipient of a Grant for Multiple Sclerosis Innovation (GMSI), Merck KGaA, is funded by a Merit Review grant (federal award document number (FAIN) BX005664-01 from the United States (U.S.) Department of Veterans Affairs, Biomedical Laboratory Research and Development, is funded by RFA-220339314 (PI) and RFA-220339305 (co-PI) grants from the National Multiple Sclerosis Society (NMSS)