Literature DB >> 8923125

Comparative studies with milnacipran and tricyclic antidepressants in the treatment of patients with major depression: a summary of clinical trial results.

S Kasper1, Y Pletan, A Solles, A Tournoux.   

Abstract

Milnacipran is a novel antidepressant agent which selectively inhibits the reuptake of serotonin and noradrenaline. Seven randomized, double-blind trials with a comparable design have compared the efficacy and tolerability of milnacipran with that of tricyclic antidepressants (TCAs) in patients with major depression. At a dose of 50 mg twice a day, milnacipran therapy is associated with a response rate (50% reduction in Hamilton Depression Rating Scale) of 64%. The rate of response to TCAs in these studies was 67%. In contrast to the TCAs, milnacipran was very well tolerated by the patients. The only adverse event that occurred more frequently in milnacipran-treated patients than in TCA-treated patients was dysuria (2.1% of patients treated with milnacipran). Milnacipran is as effective as TCAs in the treatment of patients with major depression and is better tolerated. Milnacipran's lack of effects on cardiovascular function offers improved safety in cases of overdose.

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Year:  1996        PMID: 8923125     DOI: 10.1097/00004850-199609004-00005

Source DB:  PubMed          Journal:  Int Clin Psychopharmacol        ISSN: 0268-1315            Impact factor:   1.659


  12 in total

1.  Stimulation of catecholamine synthesis via activation of p44/42 MAPK in cultured bovine adrenal medullary cells by milnacipran.

Authors:  Koji Shinkai; Yumiko Toyohira; Reiji Yoshimura; Masato Tsutsui; Susume Ueno; Jun Nakamura; Nobuyuki Yanagihara
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2007-01-09       Impact factor: 3.000

2.  Pharmacodynamics of milnacipran in young and elderly volunteers.

Authors:  I Hindmarch; U Rigney; N Stanley; M Briley
Journal:  Br J Clin Pharmacol       Date:  2000-02       Impact factor: 4.335

3.  Lack of interaction of milnacipran with the cytochrome p450 isoenzymes frequently involved in the metabolism of antidepressants.

Authors:  Christian Puozzo; Simone Lens; Christian Reh; Karl Michaelis; Dominique Rosillon; Xavier Deroubaix; Dominique Deprez
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 6.447

4.  Remission rates with milnacipran 100 mg/day and 150 mg/day in the long-term treatment of major depression.

Authors:  Kazuo Okumura; Toshiaki A Furukawa
Journal:  Clin Drug Investig       Date:  2006       Impact factor: 2.859

5.  Urinary Side Effects of Duloxetine in the Treatment of Depression and Stress Urinary Incontinence.

Authors:  Lars Viktrup; Beth A. Pangallo; Michael J. Detke; Norman R. Zinner
Journal:  Prim Care Companion J Clin Psychiatry       Date:  2004

Review 6.  Milnacipran. A review of its use in depression.

Authors:  C M Spencer; M I Wilde
Journal:  Drugs       Date:  1998-09       Impact factor: 9.546

7.  Double-blind, comparative study of milnacipran and paroxetine in Japanese patients with major depression.

Authors:  Kunitoshi Kamijima; Shinji Hashimoto; Eiichi Nagayoshi; Tsukasa Koyama
Journal:  Neuropsychiatr Dis Treat       Date:  2013-04-26       Impact factor: 2.570

8.  Milnacipran: a unique antidepressant?

Authors:  Siegfried Kasper; Gerald Pail
Journal:  Neuropsychiatr Dis Treat       Date:  2010-09-07       Impact factor: 2.570

9.  Milnacipran for the management of fibromyalgia syndrome.

Authors:  Michelle J Ormseth; Anne E Eyler; Cara L Hammonds; Chad S Boomershine
Journal:  J Pain Res       Date:  2010-03-01       Impact factor: 3.133

10.  Rapid improvement of depressive symptoms in suicide attempters following treatment with milnacipran and tricyclic antidepressants - a case series.

Authors:  Eiji Kirino; Masao Gitoh
Journal:  Neuropsychiatr Dis Treat       Date:  2011-12-14       Impact factor: 2.570

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