Dapagliflozin
is adumbrated for the administration of diabetes mellitus type 2, and functions
to advance glycemic ascendancy in adults if accumulated with diet and exercise.
Dapagliflozin is a sodium-glucose cotransporter 2 inhibitor, which prevents
glucose reabsorption in the kidney. Using dapagliflozin leads to abundant
glycosuria (glucose elimination in the urine), which can advance to weight
accident and tiredness. Dapagliflozin was accustomed by the FDA on Jan 08,
2014. Dapagliflozin is not recommended for patients with type 1 diabetes
mellitus or for the analysis of diabetic ketoacidosis.
In
July 2011 a U.S. Food and Biologic Administration (FDA) endocrinologic and
metabolic drugs advising board recommended adjoin approval until added extracts
were available.
The
FDA accustomed dapagliflozin on January 8, 2014 for glycemic control, forth
with diet and exercise, in adults with type 2 diabetes.
In
2012, the Board for Medicinal Products for Human Use (CHMP) of the European
Medicines Agency issued a absolute assessment on the drug. It is now marketed
in a amount of European countries.
The
FDA accustomed the aggregate artefact dapagliflozin and metformin hydrochloride
extended-release, called Xigduo XR, in October 2014.
In
Feb 2017 the FDA accustomed a once-daily aggregate of dapagliflozin 10 mg and
saxagliptin 5 mg, as Qtern.
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