4.3 Review

A review of the efficacy and safety of oral antidiabetic drugs

Journal

EXPERT OPINION ON DRUG SAFETY
Volume 12, Issue 2, Pages 153-175

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/14740338.2013.752813

Keywords

alpha-glucosidase inhibitor; bile-acid sequestrant; bromocriptine; DPP-4 inhibitor; meglitinide; metformin; sulfonylurea; thiazolidinedione; type 2 diabetes

Funding

  1. NCRR NIH HHS [M01 RR000095] Funding Source: Medline
  2. NHLBI NIH HHS [P01 HL056693] Funding Source: Medline
  3. NIDDK NIH HHS [R01 DK069803, P30 DK079637] Funding Source: Medline

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Introduction: Additional oral antidiabetic agents to metformin, sulfonylureas (SU) and thiazolidinediones (TZD) are approved for the treatment of type 2 diabetes. Areas covered: The efficacy and safety of metformin, SUs, TZDs, dipeptidyl peptidase-IV (DPP-4) inhibitors, meglitinide analogs, alpha-glucosidase inhibitors (AGIs), bile-acid sequestrants (BAS) and bromocriptine will be reviewed. Expert opinion: Several new oral agents have been approved for type 2 diabetes management in recent years. It is important to understand the efficacy and safety of these medications in addition to the older agents to best maximize oral drug therapy for diabetes. Of the recently introduced oral hypoglycemic/antihyperglycemic agents, the DPP-4 inhibitors are moderately efficacious compared with mainstay treatment with metformin with a low side-effect profile and have good efficacy in combination with other oral agents and insulin. They are a recommended alternative when metformin use is limited by gastrointestinal (GI) side effects or when SU treatment results in significant hypoglycemia or weight gain. Meglitinide analogs are limited by their frequent dosing, expense and hypoglycemia (repaglinide > nateglinide), while AGIs are also limited by their dosing schedule and GI side-effect profile. BAS and bromocriptine have the lowest efficacy with regard to HbA(1c) reduction, also are plagued by GI adverse reactions, but have a low risk of hypoglycemia.

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