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The FDAs Adverse Event Reporting System (FAERS) database includes 442 cases of adverse events associated with compounded semaglutide, including seven deaths

Results of a 2022 study using the IQVIA LRx database for the United Kingdom (UK) and Germany were similar to those of this study, with 66% to 72% and 71% to 81% of incident and prevalent users, respectively, receiving dulaglutide 1.5 mg post-index [13]