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FDA Confirms They Asked Pfizer to Stop Celebrex Advertising

Dec. 21, 2004 – The Food and Drug Administration has confirmed that on December 17 the agency asked Pfizer, Inc. to voluntarily suspend advertising on Celebrex during the time the FDA is obtaining and evaluating the new and conflicting scientific data on adverse events associated with the drug. Pfizer agreed with the request.

The  FDA also requested the company change the information provided to physicians to reflect the recommendations FDA made encouraging physicians to consider alternative therapies as they evaluate their individual patient needs.

Pfizer agreed to the broad suspension of its Celebrex promotion and to craft appropriate detailing to physicians that reflects the uncertainty of scientific data currently available, according to the FDA.

Related Stories

FDA Delays Action on Celebrex, Waiting for More Info

Dec. 18, 2004 – Late yesterday the Food and Drug Administration issued a statement on the warning issued by Pfizer of possible heart problems caused by their drug Celebrex, which is taken my millions of senior citizens for pain relief, primarily that caused by arthritis. The FDA says they are taking no regulatory action now but will seek more information. More... 12/18/04*

NIH Halts Use of COX-2 Inhibitor in Large Cancer Prevention Trial

Dec. 18, 2004 - The National Institutes of Health (NIH) announced Friday that it has suspended the use of COX-2 inhibitor celecoxib (Celebrex™ Pfizer, Inc.) for all participants in a large colorectal cancer prevention clinical trial conducted by the National Cancer Institute (NCI). More... 12/18/04*

Celebrex Caused Increase Heart Problem Risk: Pfizer

Dec. 17, 2004 – Celebrex has been found to cause increased risk of heart problems, according to an announcement by Pfizer, maker of the painkiller. Often used by senior citizens with arthritis, Celebrex is in the same class as the Vioxx, the drug yanked off the market in September because of similar concerns. More, including complete company statement... 12/17/04*

Pfizer Claims Celebrex Safety in September: Day Vioxx Recalled

Dec. 17, 2004 – On September 30, the day Merck & Co. announced the recall of its COX-2 drug, Vioxx, Pfizer issued a news release expressing confidence that Celebrex did not cause heart problems, as found in the case of Vioxx. More... 12/17/04*

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