Dapagliflozin/saxagliptin/metformin, sold under the brand name Qternmet XR among others, is a fixed-dose combination anti-diabetic medication used as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes.[1][2] It is a combination of dapagliflozin, saxagliptin, and metformin.[1][2] It is taken by mouth.[1][2] The drug is marketed by AstraZeneca.[3]
The most common side effects include infections of the nose and throat, hypoglycaemia (low blood sugar) when used with a sulphonylurea and effects on the gut such as nausea (feeling sick), vomiting, diarrhoea, abdominal (tummy) pain and loss of appetite.[2]
Dapagliflozin/saxagliptin/metformin was approved for medical use in the United States in May 2019, and in the European Union in November 2019.[4][2][5] Its marketing authorisation was withdrawn in the European Union in August 2020, and its approval was withdrawn in the US in April 2021, in both cases at the request of AstraZeneca.[6][7]
Medical uses
In the United States, dapagliflozin/saxagliptin/metformin is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes.[1]
In the European Union it is indicated in adults aged 18 years and older with type 2 diabetes:
References
- Qternmet XR- dapagliflozin saxagliptin and metformin hydrochloride tablet, film coated DailyMed, 24 January 2020, retrieved 14 July 2020^
- Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged. Qtrilmet EPAR European Medicines Agency (EMA), 16 September 2019, retrieved 14 July 2020^
- AstraZeneca Medications AstraZeneca US, Apr 2020, retrieved 30 March 2020^
- Drug Approval Package: Qternmet XR U.S. Food and Drug Administration (FDA), 27 January 2020, retrieved 14 July 2020^
- Qternmet XR approved in the US for the treatment of type-2 diabetes AstraZeneca, 3 May 2019, retrieved 14 July 2020^
- Qtrilment European Medicines Agency, 9 October 2020, retrieved 30 March 2021^
- Bristol-Meyers Squibb Company, et al.; Withdrawal of Approval of 19 New Drug Applications Federal Register, 16 March 2021, retrieved 30 March 2021^