Changing the status of drugs from prescription to over-the-counter availability

N Engl J Med. 2001 Sep 13;345(11):810-6. doi: 10.1056/NEJMra011080.

Abstract

The availability of drugs on an over-the-counter basis, including those previously available only by prescription, provides patients with improved access to effective therapies. Removal of the requirement for prescriptions saves both the health care professional and the patient time. However, the overall effect on health care costs is complex. One such effect may be that costs shift from third-party payers to patients. In addition, short-term cost savings may be offset over the long term by problems due to inappropriate use or suboptimal therapy. Optimal therapy with an over-the-counter drug requires that the consumer diagnose the underlying condition correctly and use the drug in a manner that minimizes risk. Assessment of the ability of patients to use drugs in this manner is a critical component of the regulatory review of over-the-counter drugs. The available data arouse the concern that without the supervision of a health care professional, some patients may not be able to use over-the-counter drugs appropriately for certain diagnoses or chronic conditions or in high-risk situations. On the other hand, the widespread use of over-the-counter aspirin on a long-term basis for cardiovascular-risk reduction illustrates the potential value of increased drug availability for long-term therapy. Advances in technology may facilitate the growth of over-the-counter drug therapy. For example, the wide availability and acceptance of reliable methods for measuring serum cholesterol in nonmedical settings may eventually contribute to the safety and effectiveness of over-the-counter treatments for hyperlipidemia. Thus, the future promises increases in the number of drugs available over the counter and in the variety of indications for their use.

Publication types

  • Historical Article
  • Review

MeSH terms

  • Drug Approval* / history
  • Drug Evaluation / legislation & jurisprudence
  • Drug Prescriptions* / history
  • Health Care Costs
  • History, 20th Century
  • Humans
  • Legislation, Drug / history
  • Marketing of Health Services / legislation & jurisprudence
  • Nonprescription Drugs* / adverse effects
  • Nonprescription Drugs* / economics
  • Nonprescription Drugs* / standards
  • Nonprescription Drugs* / therapeutic use
  • Risk
  • Self Medication
  • United States
  • United States Food and Drug Administration / history

Substances

  • Nonprescription Drugs