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Regulatory agencies including the FDA continue to monitor safety data from clinical trials and post-marketing surveillance

I am aware that a recent investigation a disproportionality analysis of World Health Organization records has gathered media attention by reporting once again a possible safety issue with suicide in GLP-1 RA users

This centralized litigation represents patients claiming a range of injuries related to GLP-1 drugs, like Trulicity

Eng personally secured a patent and partnered with Amylin, leading to the FDA-approved diabetes drug exenatide in 2005, the first GLP-1 analog

[DOI] [PMC free article] [PubMed] [Google Scholar] 60.Malinin T., Ouellette E.A