After reviewing the results of meta-analytic study evaluating data from clinical trials of antidepressant treatment in adults by the U.S. FDA recommended that the Pharmacovigilance Working Party of the European Medicines Agency (PhVWP) facfe accompanying text editing all antidepressants.
To maintain the benefits of treatment facfe superiority facfe over its risks, SIDC in cooperation with the holder of the marketing authorization of medicinal products from a group of antidepressants, ATC N06A, indicated for the treatment facfe of depressive disorders, respectively. treatment of other psychiatric disorders, gradually makes changes to texts accompanying the products. The expected date of the change at all SPC by the end of 2008.
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