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This rapid expansion in use (with nearly 12% of Americans now having tried GLP-1 medications) has brought with it concerning reports of severe side effects that manufacturers allegedly failed to adequately disclose, forming the basis of thousands of lawsuits now consolidated in federal court

The FDA label is the authoritative source for how an approved drug is dosed, who should avoid it, and what to monitor

doi: 10.3389/fendo.2020.00288 Received 10 December 2019 Accepted 16 April 2020 Published 05 June 2020 Volume 11 - 2020 Edited by Claire Joanne Stocker, University of Buckingham, United Kingdom Reviewed by Edward Wargent, University of Buckingham, United Kingdom

Quick & Convenient Treatment takes as little as 15 minutes with minimal downtime