Venlafaxine: A 2003 update

被引:87
作者
Gutierrez, MA
Stimmel, GL
Aiso, JY
机构
[1] Univ So Calif, Sch Pharm, Los Angeles, CA 90089 USA
[2] Univ So Calif, Sch Med, Los Angeles, CA USA
[3] JANEN Clin Pharm Consultants, S Pasadena, CA USA
关键词
venlafaxine; venlafaxine XR; antidepressant; treatment remission; treatment-resistant depression; generalized anxiety disorder;
D O I
10.1016/S0149-2918(03)80210-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Venlafaxine has been available for use as an antidepressant in the United States for a decade. Objective: Comprehensive reviews of venlafaxine have been published elsewhere; thus, this update focuses on newer issues of treatment remission in depression, treatment-resistant depression, and extended-release venlafaxine for generalized anxiety disorder (GAD). Methods: Relevant clinical literature from 1993 through 2003 was identified from database searches of MEDLINE and International Pharmaceutical Abstracts, and from manual searches of reference lists of the identified papers. Search terms included venlafaxine extended-release, venlafaxine XR, treatment-resistant depression, depressive disorders, anxiety disorders, generalized anxiety disorder, and antidepressive agents second generation. Results: With its dual action of serotonin and noradrenergic reuptake inhibition, venlafaxine has been shown to be superior in efficacy to selective serotonin reuptake inhibitors for severe major depressive disorder, treatment-resistant depression, and depressive symptom remission. Its demonstrated efficacy for both short- and long-term treatment of GAD has led to its use for obsessive-compulsive disorder and chronic pain syndromes, although inadequate clinical literature currently exists to support these latter 2 uses. In the past decade, no new or unexpected adverse events have been identified with venlafaxine therapy, except a possibly greater risk of fatal overdose compared with other serotonergic drugs, suggesting the need for caution in patients with suicidal ideation. Because venlafaxine is a potent serotonin agonist, caution must also be exercised to prevent the possibility of serotonin syndrome when used with other serotonin agonists, and its dose should be tapered very gradually to minimize the risk of a serotonin withdrawal reaction. Conclusion: Venlafaxine has emerged as a successful post-SSRI-era antidepressant with an expanded range of uses since it was first marketed.
引用
收藏
页码:2138 / 2154
页数:17
相关论文
共 74 条
[1]   Venlafaxine versus clomipramine in the treatment of obsessive-compulsive disorder: A preliminary single-blind, 12-week, controlled study [J].
Albert, U ;
Aguglia, E ;
Maina, G ;
Bogetto, F .
JOURNAL OF CLINICAL PSYCHIATRY, 2002, 63 (11) :1004-1009
[2]   Venlafaxine extended release (ER) in the treatment of generalised anxiety disorder - Twenty-four-week placebo-controlled dose-ranging study [J].
Allgulander, C ;
Hackett, D ;
Salinas, E .
BRITISH JOURNAL OF PSYCHIATRY, 2001, 179 :15-22
[3]  
[Anonymous], 2000, Am J Psychiatry, V157, P1
[4]  
Augustin BG, 1997, PHARMACOTHERAPY, V17, P511
[5]  
Ballenger JC, 2001, J CLIN PSYCHIAT, V62, P11
[6]  
Bandelow Borwin, 2002, World J Biol Psychiatry, V3, P171, DOI 10.3109/15622970209150621
[7]   Serotonin syndrome induced by venlafaxine and fluoxetine: A case study in polypharmacy and potential pharmacodynamic and pharmacokinetic mechanisms [J].
Bhatara, VS ;
Magnus, RD ;
Paul, KL ;
Preskorn, SH .
ANNALS OF PHARMACOTHERAPY, 1998, 32 (04) :432-436
[8]  
Blier P, 2001, J CLIN PSYCHIAT, V62, P7
[9]   Fatal toxicity of serotoninergic and other antidepressant drugs: analysis of United Kingdom mortality data [J].
Buckley, NA ;
McManus, PR .
BRITISH MEDICAL JOURNAL, 2002, 325 (7376) :1332-1333
[10]  
Davidson JRT, 2001, J CLIN PSYCHIAT, V62, P46