Pharmacopsychiatry 2015; 48(06): 187-199
DOI: 10.1055/s-0035-1555879
Review
© Georg Thieme Verlag KG Stuttgart · New York

Desvenlafaxine for the Acute Treatment of Depression: A Systematic Review and Meta-analysis

Authors

  • Z. G. Laoutidis

    1   Department of Psychiatry and Psychotherapy, Medical Faculty of the Heinrich Heine University, Düsseldorf, Germany
  • K. T. Kioulos

    2   Eginition Hospital, 1st Department of Psychiatry, Medical Faculty, University of Athens, Vasilissis Sofias Avenue, Athens, Greece
Further Information

Publication History

received 13 March 2015
revised 10 May 2015

accepted 10 June 2015

Publication Date:
23 July 2015 (online)

Abstract

Introduction: Desvenlafaxine, the active metabolite of venlafaxine, was approved in 2008 by the FDA for the treatment of depression. The aim of the present review is to provide an overview of the existing trials with desvenlafaxine and assess its overall efficacy and tolerability.

Methods: We searched in PubMed, EMBASE and the Cochrane Library for eligible studies (double-blind randomized control trials). A random effects model was used for the estimation of effect sizes.

Results: 17 trials were found in total. In the placebo-controlled trials the overall risk ratio for response was 1.24 (1.16–1.32, p<0.001), for remission 1.29 (1.16–1.43, p<0.001), for dropouts 1.16 (0.99–1.35, p=0.066) and for dropouts due to adverse events 1.98 (1.45–2.69, p<0.001). There were no differences between the various doses that were used (i. e., 50 mg, 100 mg, 200 mg, 400 mg). The mean risk ratio for response in the head-to-head trials was 0.90 (0.82–0.98, p=0.014) and for remission 0.82 (0.71–0.95, p=0.009).

Discussion: The risk ratios for response and remission were moderate. We further provide some evidence that desvenlafaxine might not be as efficacious as other antidepressants.