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BMJ 2004;329:1411 (11 December), doi:10.1136/bmj.329.7479.1411
| The first 150 words of the full text of this article appear below. |
The recent withdrawal of rofecoxib (Vioxx) from the worldwide market has focused intense public scrutiny on drug safety. Although the US Food and Drug Administration monitors drug safety after product approval, some have raised concerns about whether this system, which relies primarily upon voluntary reporting of adverse drug effects, is adequate to protect the public from unsafe pharmaceuticals.
In his televised appearance before the US Senate finance committee on 18 November, Dr David Graham, associate director in the FDA's Office of Drug Safety, claimed his own agency was "incapable of protecting [the public]" from other dangerous pharmaceuticals (
BMJ
2004;329: 1253
Carl Schoenberger, pulmonologist
Bethesda, Maryland mcschoenberger@aol.com
What can you learn from this BMJ paper? Read Leanne Tite's Paper+