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Learn more about brand
vs. generic drugs
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How do brand-name
drugs and generics differ?
When scientists develop a new drug, they
give it a generic name reflecting its chemical makeup. Once
the Food and Drug Administration (FDA) approves the
drug, the manufacturer markets it with a brand or trade
name, which is usually shorter and easier to remember. A
drug company can hold exclusive patent rights to make a
drug for 20 years after its discovery. After that, other
companies can start making generic versions of the drug.
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Are
generic drugs safe?
In almost all cases, generics work as well
as their brand-name siblings, and often cost considerably
less. This is possible not because of lower quality, but because
research and advertising costs are much less for generics.
Many insurance plans encourage you to accept the generic version
of a drug whenever it's medically safe. Most doctors prescribe
or let pharmacists substitute a generic when appropriate.
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Sources:
- Law Notes. FDA Position on Product Selection for "Narrow
Therapeutic Index" Drugs, American Journal of Health-System
Pharmacy 54 (1997).
- Levy G. "What are Narrow Therapeutic Index Drugs?"
Clinical Pharmacology & Therapeutics May (1998).
- Mayo Clinic Family Health Book. William Morrow &
Co., 1996.
- Merck Manual of Medical Information: Home Edition. Merck
& Co., 1997.
- Yorke, J. "FDA Ensures Equivalence of Generic Drugs,"
FDA Consumer Special Report on New Drug Development in
the United States Special Ed. January (1995).
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