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Abstract Background Glucagon-like peptide-1 receptor agonists (GLP-1RA) have shown promising effects on heart failure (HF) outcomes, particularly in phenotype-specific populations
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The FDA permits compounding when patients cannot access FDA-approved alternatives due to allergies to inactive ingredients, need for a different dosage form (such as liquid instead of pills), or medication shortages
Its a promising early signal, but larger trials are still needed before extended dosing becomes a recognized standard approach
