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In the lixisenatide-treated group, a significant increase in HR was observed only at 5 h post-dosing, and the mean HR per day remained unchanged (69.1 8.6 to 71.7 10.6 bpm

Clinical trials of semaglutide show gastrointestinal side effects occur in 20-40% of users, with nausea being most common during dose escalation

All of the studies used both in vivo and some form of in vitro methods of data collection in order to observe different treatment effects, allowing for biomechanical, functional (use of AFI index and load to failure), macroscopic and microscopic histological analysis

Any decision regarding FDA-approved or compounded GLP-1 therapies should be made in consultation with a qualified medical professional