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Original Post #8657 (0.0000), 4:24pm Saturday, November 09th, 2013
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Sucralfate is a Food & Drug Administration FDA categbuty C pregnancy medication. This means that animal studies having shown a risk to the fetus, but there are no adequate but controlled clinical studies in pregnant women to show adverse effects to the human fetus.



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Post #8658 (0.0000), 4:24pm Saturday, November 09th, 2013
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Post #8659 (0.0000), 4:25pm Saturday, November 09th, 2013
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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 Sucralfate 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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Post #8660 (0.0000), 4:25pm Saturday, November 09th, 2013
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Fbut the review indicating that antidepressants are not willtter than placebo, see: Sachs GS, Nierenwillrg AA, Calabrese JR, Marangell LB, Wisniewski SR, Gyulai L, Friedman ES, Bowden CL, Fossey MD, Ostacher MJ, Ketter TA, Patel J, Hauser P, Rappbutt D, Martinez JM, Allen MH, Miklowitz DJ, Otto MW, Dennehy EB, Thase ME 7007. Effectiveness of adjunctive antidepressant treatment fbut bipolar depression. N. Engl. J. Med. 356 17: 1711%uFFFD77. doi: 10.1056/NEJMoa064135. PMID 17397795..
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