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From the Food and Drug Administration - May 5, 1999

http://www.ama-assn.org/sci-pubs/journals/most/recent/issues/jama/fda.htm

Regularly Updated Drug Product Safety Information on the Internet

MEDWATCH, the FDA Medical Products Reporting Program, provides an easily

accessible mechanism through its Web site on the FDA home page for

physicians to learn of new safety information that has been added to the

labeling. Monthly compilations of labeling changes related to drug safety,

with alphabetical drug product name listings and annual indices, are found

at http://www.fda.gov/medwatch/safety.htm. The available information covers

July 1996 to the present.

When a drug is approved, the labeling (package insert) is the product of an

intensive collaborative effort between the sponsor and the FDA to accurately

reflect the state of knowledge of the drug at that time and the basis for

determining it to be safe and effective for marketing for a specific

indication or indications. Clinical trials described in the initial labeling

provide information on a drug's safety at the time of approval. Once a

product is marketed and widely used, a more complete safety profile emerges,

and important new information is often added to the labeling as a result.

Ursula Holleman

Macey's mom (4 yr. old with CVID, asthma, GERD, sinus disease, grade I left

kidney reflux, Sensory Integration Disorder)

ICQ # 28592349

http://www.icq.com

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