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Prescribing Information Forxiga® (dapagliflozin)
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FORXIGA (dapagliflozin) | AstraZeneca UK

 

Discover the cardiorenal protective benefits of Forxiga (dapagliflozin)

 

 

About dapagliflozin

Dapagliflozin is the first sodium-glucose co-transporter-2 inhibitor (SGLT-2i) approved for the treatment of insufficiently controlled type 2 diabetes (T2D), chronic kidney disease (CKD), and symptomatic chronic heart failure (HF)

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Simple once-daily dosing. Start on 10 mg daily, stay on 10 mg daily, no need for up-titration


A starting dose of 5 mg daily is recommended for cases of severe hepatic impairment which may be increased to 10 mg if well tolerated1

Dapagliflozin is indicated for:

Type 2 Diabetes

Dapagliflozin is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled Type 2 diabetes mellitus as an adjunct to diet and exercise:1 

- as monotherapy when metformin is considered inappropriate due to intolerance. 

- in addition to other medicinal products for the treatment of type 2 diabetes.

 

Find out more

 

Access T2D Patient Resources

Chronic Kidney Disease

Dapagliflozin is indicated for the treatment of CKD in adult patients. 
 

Dapagliflozin is not recommended to be initiated in patients with eGFR < 15 mL/min/1.73m2.


With eGFR <45 mL/min/1.73 m2, additional glucose lowering treatment should be considered in patients with type 2 diabetes.

 

Find out more

 

Access CKD Patient Resources

Heart Failure

Dapagliflozin is indicated for the treatment of symptomatic chronic heart failure in adult patients.1

 

 

 

 

 

 

 

Find out more

 

Access HF Patient Resources

Safety profile

Addresses key safety considerations regarding the use of dapagliflozin in patients

Find out more

CKD: Chronic Kidney Disease; eGFR: Estimated Glomerular Filtration Rate; HF: Heart Failure; MHRA: Medicines and Healthcare products Regulatory Agency; SmPC: Summary of Product Characteristics; SGLT2i: Sodium-Glucose Co-Transporter-2 Inhibitor; T2D: Type 2 Diabetes.

  1. FORXIGA 10 mg film-coated tablets - Summary of Product Characteristics (SmPC). 

GB-70100 | September 2025

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to AstraZeneca by visiting https://contactazmedical.astrazeneca.com/ or by calling ‌‌‌0‌‌‌8‌‌‌‌‌0‌‌‌‌0‌‌‌ ‌‌7‌‌‌‌‌‌8‌‌‌3‌‌‌ ‌‌0‌‌‌‌‌0‌‌‌‌3‌‌‌‌3‌‌‌.

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