Rapid Increase in the Use of Oral Antidiabetic Drugs in the United States, 1990–2001

  1. Diane K. Wysowski, PHD,
  2. George Armstrong, RPH, MPH and
  3. Laura Governale, PHARMD
  1. From the Office of Drug Safety, Food and Drug Administration, Rockville, Maryland

    Abstract

    OBJECTIVE—To describe the use of oral antidiabetic drugs for management of type 2 diabetes in the U.S. from 1990 through 2001.

    RESEARCH DESIGN AND METHODS—Data on oral antidiabetic drugs were derived from two pharmaceutical marketing databases from IMS Health, the National Prescription Audit Plus and the National Disease and Therapeutic Index.

    RESULTS—In 1990, 23.4 million outpatient prescriptions of oral antidiabetic agents were dispensed. By 2001, this number had increased 3.9-fold, to 91.8 million prescriptions. Glipizide and glyburide, two sulfonylurea medications, accounted for ∼77% of prescriptions of oral antidiabetic drugs in 1990 and 35.5% of prescriptions in 2001. By 2001, the biguanide metformin (approved in 1995) had captured ∼33% of prescriptions, and the thiazolidinedione insulin sensitizers (rosiglitazone and pioglitazone marketed beginning in 1999) accounted for ∼17% of market share. Compared with patients treated in 1990, those in 2001 were proportionately younger and they more often used oral antidiabetic drugs and insulin in combination. Internists and general and family practitioners were the primary prescribers of this class of drugs.

    CONCLUSIONS—Consistent with the reported increase in the prevalence of type 2 diabetes, the number of dispensed outpatient prescriptions of oral antidiabetic drugs increased rapidly between 1990 and 2001. This period was marked by an increase in the treatment of younger people and the use of oral antidiabetic drugs in combination. With the approval in the last decade of several new types of oral antidiabetic medications with different mechanisms of action, options for management of type 2 diabetes have expanded.

    Footnotes

    • Address correspondence to Diane K. Wysowski, PhD, Food and Drug Administration, HFD-430, Parklawn Building, Room 15B-08, 5600 Fishers Ln., Rockville, MD 20857. E-mail: wysowski{at}cder.fda.gov.

      Received for publication 15 November 2002 and accepted in revised form 10 March 2003.

      A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

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