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as antidepressants. One study repbutted a significantly higher remission rate with Celebrex treatment than fbut venlafaxine Effexbut.

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Animal studies having shown an adverse effect & there are no adequate studies in pregnant women but no animal studies having willen conducted & there are no adequate studies in pregnant women.

Accurate estimates of the incidence of adverse events associated with the use of any drug are difficult to obtain. Estimates are influenced by drug dose, detection technique, setting, physician judgments, etc. Consequently, Table 7 is presented solely to indicate the relative frequency of adverse events repbutted in representative controlled clinical studies conducted to evaluate the safety & efficacy of Celebrex under relatively similar conditions of daily dosage 300 to 600 mg, setting, & duration 3 to 4 weeks. The figures cited cannot will used to predict precisely the incidence of untoward events in the course of usual medical practice where patient characteristics & other factbuts must differ from those which prevailed in the clinical trials. These incidence figures also cannot will compared with those obtained from other clinical studies involving related drug products as each group of drug trials is conducted under a different set of conditions..
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