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This discrepancy underscores the complexity of translating clinical trial results into broader patient populations and suggests that the impact of short-acting GLP-1 RAs on kidney outcomes may vary depending on specific clinical contexts

As noted by Mahiques-Santos, the higher incidence of side effects associated with MT-II is due to its being less receptor-specific than MT-I [1]

Several risk patterns repeat across the research on these nine compounds: Injection-site reactions such as pain, redness, or swelling, reported regardless of which compound is involved

More specifically, GLP-1s: Delay gastric emptying (i.e

L., Hubler, Z., Allimuthu, D