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doi: 10.1016/j.colsurfb.2017.11.068

Aroda VR, Ahmann A, Cariou B, Chow F, Davies MJ, Jdar E, et al

this choice may have helped avoid patients unable to access the drug due to insurance issues after initial order, but did nothing to address the question of people getting access through alternate sources external to our system

On the same date, Julian Gill also requested case numbers for all adverse events in the FAERS system related to tirzepatide and semaglutide products produced by Empower Pharmacy in Houston, Texas (both the 503A and 503B products). Noa Metta submitted on September 24 a request for FDA Form 483 inspection reports, warning letters, Establishment Inspection Reports, and adverse event reports relating to pharmacies conducting unauthorized compounding practices, involving semaglutide, tirzepatide, or similar drugs, between January 1, 2022, and the present. Several additional requests addressed non-compounding issues related to GLP-1 drugs, two mentioning Eli Lilly and one mentioning Ozempic and Wegovy