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Curr Hypertens Rep 27 , 2 (2025)

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Post-marketing surveillance and FDA Adverse Event Reporting System (FAERS) data have documented isolated reports of patients experiencing dyspnea while taking GLP-1 medications, but establishing causality remains challenging

The review discusses the importance of reducing mealtime insulin doses by 50% when initiating pramlintide to prevent hypoglycemia during the dose-titration period