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Ther Adv Drug Saf. 2014 Dec;5(6):242-54. doi: 10.1177/2042098614551938.

Dapagliflozin efficacy and safety: a perspective review.

Therapeutic advances in drug safety

Sarah L Anderson

Affiliations

  1. University of Colorado Anschutz Medical Campus, Skaggs School of Pharmacy and Pharmaceutical Sciences, 12850 East Montview Blvd, Room V20-2129, Aurora, CO 80045, USA.

PMID: 25436106 PMCID: PMC4232499 DOI: 10.1177/2042098614551938

Abstract

Type 2 diabetes mellitus is a prevalent, progressive disease with a need for innovative therapeutic agents to continue to advance disease management. Dapagliflozin is the second agent in a new class of oral antihyperglycemic drugs: sodium-glucose cotransporter 2 (SGLT2) inhibitors. SGLT2 is responsible for the majority of renal glucose reuptake; inhibition of the cotransporter allows for increased renal glucose excretion that consequently leads to reduced plasma glucose levels. Because this mechanism does not require the action of insulin, dapagliflozin rarely causes hypoglycemia and is effective in patients both early and late in the course of their disease. Studies of dapagliflozin have demonstrated efficacy both as monotherapy and in combination with oral antihyperglycemic agents and insulin. Dapagliflozin has been shown to decrease hemoglobin A1c (HbA1c) values 6 mmol/mol (0.5%) to 8 mmol/mol (0.7%). The most common adverse reactions observed with dapagliflozin in clinical trials were female genital mycotic infections, urinary tract infections, and nasopharyngitis. Dapagliflozin is a new oral agent for type 2 diabetes with short-term efficacy similar to dipeptidyl peptidase 4 inhibitors; its long-term safety and efficacy are unknown.

Keywords: dapagliflozin; hypoglycemic agents; sodium-glucose transporter 2; type 2 diabetes mellitus

References

  1. Clin Pharmacol Ther. 2009 May;85(5):520-6 - PubMed
  2. Diabetes Obes Metab. 2013 May;15(5):432-40 - PubMed
  3. Diabetes. 1995 Nov;44(11):1249-58 - PubMed
  4. J Diabetes Complications. 2013 Sep-Oct;27(5):479-84 - PubMed
  5. Diabetes Obes Metab. 2014 Feb;16(2):124-36 - PubMed
  6. Diabetes Care. 2014 Jan;37 Suppl 1:S14-80 - PubMed
  7. BMJ. 1995 Jan 14;310(6972):83-8 - PubMed
  8. Lancet. 2011 Jul 2;378(9785):31-40 - PubMed
  9. Diabetologia. 2012 Jun;55(6):1577-96 - PubMed
  10. Diabetes Care. 2013 Aug;36(8):2271-9 - PubMed
  11. Diabetes Obes Metab. 2012 Oct;14(10):951-9 - PubMed
  12. Diabetes Care. 2010 Oct;33(10):2217-24 - PubMed
  13. Diabetes Care. 2011 Sep;34(9):2015-22 - PubMed
  14. Diabetes Obes Metab. 2011 Jan;13(1):47-54 - PubMed
  15. Diabetes Care. 2014;37(3):740-50 - PubMed
  16. Diabetes Obes Metab. 2011 Apr;13(4):357-65 - PubMed
  17. Diabetes Obes Metab. 2010 Jun;12(6):510-6 - PubMed
  18. Diabetes Obes Metab. 2011 Oct;13(10):928-38 - PubMed
  19. Pflugers Arch. 2004 Feb;447(5):510-8 - PubMed
  20. Diabetes Care. 2012 Jul;35(7):1473-8 - PubMed
  21. PLoS Med. 2006 Nov;3(11):e442 - PubMed
  22. Kidney Int. 2014 Apr;85(4):962-71 - PubMed
  23. Br J Clin Pharmacol. 2013 Sep;76(3):432-44 - PubMed
  24. Hum Genet. 2002 Dec;111(6):544-7 - PubMed
  25. Diabetes Care. 2009 Sep;32(9):1656-62 - PubMed
  26. Int J Antimicrob Agents. 2008 Feb;31 Suppl 1:S54-7 - PubMed
  27. Am J Physiol Renal Physiol. 2001 Jan;280(1):F10-8 - PubMed
  28. Lancet. 2010 Jun 26;375(9733):2223-33 - PubMed
  29. J Diabetes Complications. 2013 Sep-Oct;27(5):473-8 - PubMed
  30. Diabetes Care. 2013 Oct;36(10):3169-76 - PubMed
  31. Int J Clin Pract. 2012 May;66(5):446-56 - PubMed
  32. Diabetes Care. 2009 Apr;32(4):650-7 - PubMed

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