Indication

Heart failure associated with type 2 diabetes mellitus

Heart failure associated with type 2 diabetes mellitus is a high-risk cardiovascular complication characterized by the inability of the heart to maintain adequate systemic perfusion or to do so only under elevated filling pressures in individuals with type 2 diabetes mellitus. Read more about Heart failure associated with type 2 diabetes mellitus

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Drugs that treat it

Common Heart failure associated with type 2 diabetes mellitus therapies.

Showing 19–25 of 25 drugs

DAPAGLIFLOZIN

ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT-2 (SGLT2) INHIBITORS·TYPE 2 DIABETES MELLITUS·+4
NOVADOZ PHARMAC

DAPAGLIFLOZIN

ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT-2 (SGLT2) INHIBITORS·TYPE 2 DIABETES MELLITUS·+4
SANDOZ

DAPAGLIFLOZIN

ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT-2 (SGLT2) INHIBITORS·TYPE 2 DIABETES MELLITUS·+4
TEVA PHARM

DAPAGLIFLOZIN

ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT-2 (SGLT2) INHIBITORS·TYPE 2 DIABETES MELLITUS·+4
BIOCON PHARMA I

DAPAGLIFLOZIN

ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT-2 (SGLT2) INHIBITORS·TYPE 2 DIABETES MELLITUS·+4
ANI PHARMACEUTI

DAPAGLIFLOZIN

ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT-2 (SGLT2) INHIBITORS·TYPE 2 DIABETES MELLITUS·+4
AVKARE

DAPAGLIFLOZIN

ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT-2 (SGLT2) INHIBITORS·TYPE 2 DIABETES MELLITUS·+4
MICRO LABS USA,
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About Heart failure associated with type 2 diabetes mellitus.

Heart failure associated with type 2 diabetes mellitus is a high-risk cardiovascular complication characterized by the inability of the heart to maintain adequate systemic perfusion or to do so only under elevated filling pressures in individuals with type 2 diabetes mellitus.

Affecting the cardiovascular and metabolic systems, this clinical state can manifest across preserved, mildly reduced, or reduced left ventricular ejection fraction phenotypes.

Pathophysiologically, persistent hyperglycemia, hyperinsulinemia, and insulin resistance induce myocardial lipotoxicity, advanced glycation end-product accumulation, systemic microvascular inflammation, and neurohormonal overactivation.

These interrelated mechanisms drive myocardial fibrosis, adverse ventricular remodeling, and impaired diastolic and systolic function, substantially increasing the risk of cardiovascular mortality and hospitalizations.

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