http://bmj.com/cgi/content/full/325/7364/0/g
| Home | Help | Search/Archive | Feedback | Table of Contents |
Alosetron (Lotronex)
a
drug for irritable bowel syndrome
was
withdrawn from sale in the United States in late 2000 after reports
of serious adverse events, but six weeks later the special joint
advisory committee to the United States Food and Drug Administration
(FDA) recommended its remarketing. A senior advisor from the committee
has warned of more deaths if the drug is relaunched, and a former
insider of the FDA says that the agency has become a servant of
the pharmaceutical industry. On p
592 Moynihan charts the path of the drug and examines the truth
or otherwise of inappropriate corporate influence in drug licensing.
|
| (Credit: MARTY KATZ) |
| Home | Help | Search/Archive | Feedback | Table of Contents |
ALL INFORMATION, DATA, AND
MATERIAL CONTAINED, PRESENTED, OR PROVIDED HERE IS FOR GENERAL INFORMATION
PURPOSES ONLY AND IS NOT TO BE CONSTRUED AS REFLECTING THE KNOWLEDGE OR OPINIONS
OF THE PUBLISHER, AND IS NOT TO BE CONSTRUED OR INTENDED AS PROVIDING MEDICAL OR
LEGAL ADVICE. THE DECISION WHETHER OR NOT TO VACCINATE IS AN IMPORTANT AND
COMPLEX ISSUE AND SHOULD BE MADE BY YOU, AND YOU ALONE, IN CONSULTATION WITH
YOUR HEALTH CARE PROVIDER.