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Mansergh G, Shouse RL, Marks G, Guzman R, Rader M, Buchbinder S, Colfax GN.

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On April 7, 2005, the Food and Drug Administration (FDA) asked Pfizer to voluntarily remove Bextra (valdecoxib) from the market.

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In the pregnant rat, the AUC for calculated free drug at this dose was approximately 18 times the human AUC at a 20 mg dose.

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The drug treatment also delayed an injury-related decline in the heart's output of pumped blood, the Virginia cardiologists reported in the January Pediatric Research.

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