All drug referencesSGLT2 inhibitor

Dapagliflozin (Farxiga, Forxiga)

Dapagliflozin is an SGLT2 inhibitor with indications spanning T2DM glycemic control, heart failure across the ejection-fraction spectrum, and CKD regardless of diabetes status. Its evidence base (DAPA-HF, DELIVER, DAPA-CKD) established SGLT2 inhibitors as a cardio-renal-metabolic class.

Mechanism of action
Selective inhibition of sodium-glucose cotransporter 2 in the proximal tubule, producing glycosuria, natriuresis, modest blood pressure reduction, and neurohormonal modulation.
Administration route
Oral, once daily

FDA-approved indications (2026)

  • Type 2 diabetes

    Glycemic control in adults and pediatrics ≥10 years.

  • Heart failure

    Reduction of CV death and HF hospitalization across the EF spectrum (HFrEF — DAPA-HF; HFpEF/HFmrEF — DELIVER).

  • Chronic kidney disease

    Reduction of kidney function decline, kidney failure, CV death, and HF hospitalization in CKD with or without T2DM (DAPA-CKD).

Dosing: adult, renal, and hepatic

PopulationDose
T2DM / HF / CKD10 mg PO once daily. For glycemic control only, may start at 5 mg.
Renal impairmentInitiate if eGFR ≥25 mL/min/1.73 m² for CKD/HF indications. Do not initiate for glycemic benefit at eGFR <45. Continue until dialysis.
Hepatic impairmentNo dose adjustment in mild/moderate. Use caution in severe hepatic impairment; benefit/risk evaluation.

Contraindications and boxed warnings

Contraindications

  • Serious hypersensitivity to dapagliflozin.
  • Dialysis.

2026 guideline and pivotal trial position

2026 ACC/AHA/HFSA heart failure guidance positions SGLT2 inhibitors as one of the four pillars of GDMT across the EF spectrum. KDIGO 2024 lists dapagliflozin as a first-line agent in CKD with proteinuria regardless of diabetic status. ADA 2026 co-recommends SGLT2 inhibitors with GLP-1 RAs for T2DM with CV/renal disease.

DAPA-HF

26% RRR in CV death or worsening HF in HFrEF.

DELIVER

18% RRR in CV death or worsening HF in HFmrEF/HFpEF (EF >40%).

DAPA-CKD

39% RRR in composite kidney outcome in CKD with or without diabetes.

Cross-system reasoning

Dapagliflozin's benefit extends from cardiology (HF hospitalization reduction) to nephrology (kidney function preservation) to endocrinology (glycemic control and modest weight loss). In a patient with HFpEF and CKD stage 3b without diabetes, dapagliflozin is still indicated — a decision that crosses cardiology-nephrology lines. Recognize euglycemic DKA risk (hold perioperatively or during prolonged fasting), genitourinary infection screening, and modest volume-depletion effect that may warrant diuretic dose reduction at initiation.

Key references

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This reference is for US-licensed physicians and is not a substitute for the full FDA prescribing information. Dosing in special populations, drug interactions, and emerging safety information should be verified against the current manufacturer label and society guidelines before prescribing.