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Egito is a fixed-dose combination (FDC) therapy developed by the Brazilian pharmaceutical company EMS for the treatment of patients with type 2 diabetes mellitus and hypertension. It combines two well-established pharmacological agents: empagliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, and telmisartan, an angiotensin II receptor blocker (ARB). Empagliflozin works by reducing renal glucose reabsorption in the proximal tubules, leading to increased urinary glucose excretion and lower blood glucose levels. Telmisartan acts by selectively blocking the binding of angiotensin II to the AT1 receptor, which results in vasodilation and a reduction in blood pressure. This combination is intended to simplify treatment regimens and improve clinical outcomes in patients who require management of both metabolic and cardiovascular risk factors.
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