Dapagliflozin
Brand names: Forxiga
Dapagliflozin is an SGLT2 inhibitor used in type 2 diabetes and, independently of diabetes, in heart failure and chronic kidney disease, where it has cardiovascular and renal benefits.
Adult dose
Dose adjustments
eGFR 45 or greater: for glycaemic control start 5 mg once daily, may increase to 10 mg; for all other indications 10 mg once daily. eGFR 25 to less than 45: 10 mg once daily. eGFR less than 25: initiation not recommended; patients may continue 10 mg once daily to reduce risk of eGFR decline, ESKD, CV death and hospitalisation for heart failure.
Dose auto-extracted from US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
US labelling (FDA)
Reference — US labelling, may differ from UK• Assess volume status and correct volume depletion before initiating. (2.1) eGFR (mL/min/1.73 m 2 ) Recommended Dose eGFR 45 or greater To improve glycemic control, the recommended starting dose is 5 mg orally once daily. Dose can be increased to 10 mg orally once daily for additional glycemic control. For all other indications, the recommended starting dose is 10 mg orally once daily. eGFR 25 to less than 45 10 mg orally once daily eGFR less than 25 Initiation is not recommended; however, patients may continue 10 mg orally once daily to reduce the risk of eGFR decline, ESKD, CV death and hHF. • Withhold FARXIGA for at least 3 days, if possible, prior to major surgery or procedures …
Source: US FDA prescribing information (openFDA / DailyMed), label dated 2023-12-12. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.
Contraindications
- History of a serious hypersensitivity reaction to dapagliflozin, such as anaphylactic reactions or angioedema
Side effects
- Female genital mycotic infections
- Nasopharyngitis
- Urinary tract infections
- Volume depletion / hypotension
- Diabetic ketoacidosis (including in type 1 diabetes and others at risk)
Interactions
- Insulin or insulin secretagogues (e.g. sulfonylurea): increased risk of hypoglycaemia; may require lower doses of insulin or the secretagogue
- Lithium: concomitant use with an SGLT2 inhibitor may decrease serum lithium concentrations; monitor lithium more frequently during initiation and dose changes
- Positive urine glucose test and 1,5-anhydroglucitol (1,5-AG) assay: unreliable in patients on SGLT2 inhibitors; use alternative methods to monitor glycaemic control
Clinical monograph
How it works
It blocks the sodium-glucose co-transporter 2 in the proximal renal tubule, increasing urinary glucose and sodium excretion; its heart-failure and kidney benefits are only partly explained by glucose lowering.
Prescribing in practice
- There is a risk of diabetic ketoacidosis, which can occur with near-normal glucose — withhold during acute illness, fasting or surgery (sick-day rules) and counsel on warning symptoms.
- Genital and urinary infections and volume depletion can occur, especially with diuretics; a small early dip in eGFR is expected and not a reason to stop.
- It is not relied upon for glucose lowering at low eGFR, though cardiorenal indications extend to lower eGFR thresholds.
Monitoring
Monitor renal function and volume status; remain alert to ketoacidosis symptoms regardless of blood glucose.
Counselling the patient
- Follow sick-day rules — stop temporarily if you are acutely unwell, vomiting, or not eating, and seek advice.
- Maintain genital hygiene and report symptoms of infection.
- Seek urgent help for nausea, vomiting, abdominal pain or breathlessness even if your sugar is normal.
Evidence & guidelines
SGLT2 inhibitors are recommended in HFrEF and in CKD (e.g. DAPA-HF, DAPA-CKD) and in type 2 diabetes with cardiovascular risk, per NICE guidance.
Reference: DAPA-HF (McMurray et al, NEJM 2019); DAPA-CKD (Heerspink et al, NEJM 2020); NICE TA679; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- SCORE2-Diabetes 10-Year CVD Risk in Type 2 Diabetes · Cardiovascular Risk
- PCP-HF Risk Score (Pooled Cohort Equations to Prevent Heart Failure) · Heart Failure Prevention
- SMART Risk Score for Recurrent CVD · Cardiovascular Risk
- PCSK9 Inhibitor Eligibility Assessment · Lipid Management
- Immune-Related Adverse Events (irAE) -- GI Toxicity Colitis Grading · Oncology-Related GI
- irAE Hepatitis Grading (CTCAE) · Immunotherapy
- Acute Heart Failure · ESC 2021 Heart Failure Guidelines; NICE NG106
- NSTEMI / Unstable Angina · ESC 2020 NSTEMI Guidelines; NICE NG185
- New-Onset Atrial Fibrillation · ESC 2020 AF Guidelines; NICE NG196
- Hypertensive Emergency · ESC/ESH 2018 Hypertension Guidelines; NICE NG136
- Bradycardia Management · Resuscitation Council UK ABCDE; ESC 2021 Pacing Guidelines
- Ventricular Tachycardia / Fibrillation · Resuscitation Council UK ACLS; ESC 2022 Ventricular Arrhythmia Guidelines