In the United States, consumers legally have access to drugsby two mechanisms: access with a prescription provided by alicensed health care professional or access without a prescription,by over-the-counter purchase. Many other countries have a similarclassification of drugs. In addition, some countries have athird mechanism, by which certain sales without a prescriptionrequire consultation with a pharmacist or in which the marketingof certain drugs is limited to venues where such consultationis available. It was estimated that in 2000, consumers in theUnited States spent approximately $19.1 billion on over-the-counterdrugs.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, HarborUCLA Medical Center, Torrance, Calif.
Address reprint requests to Dr. Brass at the Department of Medicine, HarborUCLA Medical Center, 1124 W. Carson St., Torrance, CA 90502, or at ebrass@ucla.edu.
References
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