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Review Article
Drug Therapy
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Volume 345:810-816 September 13, 2001 Number 11
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Changing the Status of Drugs from Prescription to Over-the-Counter Availability
Eric P. Brass, M.D., Ph.D.

Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

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In the United States, consumers legally have access to drugs by two mechanisms: access with a prescription provided by a licensed health care professional or access without a prescription, by over-the-counter purchase. Many other countries have a similar classification of drugs. In addition, some countries have a third mechanism, by which certain sales without a prescription require consultation with a pharmacist or in which the marketing of certain drugs is limited to venues where such consultation is available. It was estimated that in 2000, consumers in the United States spent approximately $19.1 billion on over-the-counter drugs.1 In recent years, more . . . [Full Text of this Article]

Regulatory Background

Evaluation of Drugs for Over-the-Counter Marketing

Effect on Health Care of Switches from Prescription-Only to Over-the-Counter Availability

Potential Benefits

            Increased Access to Effective Drugs

            Decreased Frequency of Visits to Physicians and Lower Health Care Costs

            Increases in Patients' Autonomy and Education

Areas of Concern

            Inaccurate Self-Diagnosis

            Delayed or Suboptimal Treatment of Serious Conditions

            Risks Associated with Inappropriate Drug Use

Redistribution of Health Care Costs

Diminished Role of Physicians in Supervising Care

Summary


Source Information

From the Department of Medicine, Center for Clinical Pharmacology, Harbor–UCLA Medical Center, Torrance, Calif.

Address reprint requests to Dr. Brass at the Department of Medicine, Harbor–UCLA Medical Center, 1124 W. Carson St., Torrance, CA 90502, or at ebrass@ucla.edu.

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