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Desvenlafaxine, a serotonin-norepinephrine uptake inhibitor for major depressive disorder, neuropathic pain and the vasomotor symptoms associated with menopause. Current opinion in investigational drugs (London, England : 2000) [Curr Opin Investig Drugs] Journal article

 
TitleDesvenlafaxine, a serotonin-norepinephrine uptake inhibitor for major depressive disorder, neuropathic pain and the vasomotor symptoms associated with menopause.
Author(s)Pae CU, Park MH, Marks DM, Han C, Patkar AA, Masand PS 
InstitutionDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, 2218 Elder Street, DUMC Box 3419, Durham, NC 27705, USA. pae@catholic.ac.kr.
SourceCurr Opin Investig Drugs 2009 Jan; 10(1):75-90.
AbstractDesvenlafaxine, a serotonin-norepinephrine reuptake inhibitor (SNRI) developed by Wyeth, is a novel salt form of the isolated major active metabolite of the antidepressant venlafaxine. Desvenlafaxine was developed as a slow-release tablet formulation and rapidly penetrates the brain upon administration supporting its direct effects on neuronal systems of the brain. Unlike various other antidepressants including venlafaxine, desvenlafaxine is not metabolized by cytochrome p450 (CYP) enzyme pathways and is associated with minimal inhibition of CYP enzymes. This feature results in a comparatively low risk of drug-drug interaction and consistent intra-individual and inter-individual pharmacokinetic profiles. Desvenlafaxine has been recently approved by the US FDA for the treatment of major depressive disorder (MDD) based on a series of randomized, double-blind, placebo-controlled clinical trials indicating efficacy and safety for patients with MDD. Studies have also supported the potential utility of desvenlafaxine in the treatment of vasomotor symptoms of menopause, anxiety symptoms and painful physical symptoms. However, concerns including mixed efficacy and adverse events need to be further explored in future studies.
Languageeng
Pub Type(s)Journal Article
PubMed ID19127490
  
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