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 | How do brand-name drugs and generics differ?
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|  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. 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 states let pharmacists substitute a generic when appropriate and when your doctor approves it. Our pharmacy is located in New Jersey, so we only substitute generic drugs approved under New Jersey law. When shouldn't generics be substituted for brand-name drugs?
Very few drugs have a "narrow therapeutic index," meaning that a small variation in dose can cause problems, such as too little effectiveness or too many side effects. With some drugs, including phenytoin (brand name Dilantin), carbamazepine (Tegretol), valproic acid (Depakene), divalproex sodium (Depakote), digoxin (Lanoxin), warfarin (Coumadin), lithium (Lithobid, Eskalith), levothyroxine (Synthroid, Levoxyl), and theophylline (Theo-Dur), you shouldn't switch from brand to generic—or vice versa—without your doctor's approval and close supervision. Always talk to your doctor, pharmacist, or both before asking for a substitute. 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).
CDER Consumer Information, "Generic Drugs: Questions and Answers." http://www.fda.gov/ Last accessed 12/20/2006.
This answer prepared 8/9/2000.
This information updated 12/20/2006.
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