Forxiga (dapagliflozin)
- Region
- 🇪🇺 EU
- Active substance
- dapagliflozin
- Company
- AstraZeneca AB
- Status
- Authorised
- Therapeutic area
- Diabetes Mellitus, Type 2; Heart Failure, Systolic; Heart Failure; Renal Insufficiency, Chronic
- EU approval
- Sun 11 Nov 2012
- Application
- EMEA/H/C/002322
- ATC
- A10BK01
- Official record
- www.ema.europa.eu
Indication
Type 2 diabetes mellitus Forxiga 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 as monotherapy when metformin is considered inappropriate due to intolerance. in addition to other medicinal products for the treatment of type 2 diabetes. For study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4.4, 4.5 and 5.1. Heart failure Forxiga is indicated in adults for the treatment of symptomatic chronic heart failure. Chronic kidney disease Forxiga is indicated in adults for the treatment of chronic kidney disease.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Qtern Authorised · Astra Zeneca AB
- 🇪🇺 Edistride Authorised · AstraZeneca AB
- 🇪🇺 Ebymect Authorised · AstraZeneca AB
- 🇪🇺 Xigduo Authorised · AstraZeneca AB
- 🇪🇺 Dapagliflozin Viatris Authorised · Viatris Limited
- 🇪🇺 Qtrilmet Withdrawn · AstraZeneca AB
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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.