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Timeline of Events

November 2001 - Bextra is approved by the United States Food and Drug Administration for treatment of osteoarthritis, menstrual pain, and acute pain in adults.

November 2004 – A key Cox-2 researcher is asked to leave an FDA panel after he finds that Bextra doubles the risk of heart attacks and strokes.

December 2004  - The New England Journal of Medicine states that Bextra increased the risk of serious cardiovascular outcomes (heart attacks and strokes) by a factor of approximately three.

January 2005 -- Public Citizen consumer group issues petitions to remove Bextra.

February 2005 - New England Journal of Medicine article states the use of Bextra after bypass surgery was associated with an increased incident of cardiovascular events (heart attack and stroke).

February 2005 - CBSnews.com cites a new study indicating Bextra increases the risk of heart attack and stroke by 50% .

April 2005 - Bextra is withdrawn from the market by the FDA