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These mechanisms may accelerate the pharmacokinetic changes in the affected drug and lead to clinically relevant DDIs, particularly in drugs with a narrow therapeutic window
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Since the first GLP-1 analogs received approval in 2005, these medications have demonstrated remarkable versatility
Its main side effects match those seen with Retatrutide: nausea, vomiting, and diarrhea are most common
Retatrutide is a triple agonist targeting GLP-1, GIP, and glucagon receptors simultaneously, compared to semaglutide (GLP-1 only) and tirzepatide (GLP-1 and GIP)
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