Differential period of onset of action of fluvoxamine, paroxetine and milnacipran for depression
- PMID: 12923828
- DOI: 10.1002/hup.508
Differential period of onset of action of fluvoxamine, paroxetine and milnacipran for depression
Abstract
Introduction: Selective serotonin reuptake inhibitors (SSRIs) and dual serotonin and noradrenaline reuptake inhibitors (SNRIs) are the most commonly prescribed class of antidepressants, yet it is not known whether one is superior to another.
Aims: The purpose of this clinical practice was to compare the periods of onset of action of fluvoxamine, paroxetine and milnacipran.
Methods: A retrospective cohort analysis was carried out among out-patients with depression treated in the Department of Psychiatry, Kawasaki Medical School Hospital, Kurashiki, Japan, in 2000 and 2001. A total of 206 patients receiving fluvoxamine, paroxetine and milnacipran were identified.
Results: The cumulative percentage of responders receiving milnacipran reached over 80% after 4 weeks, but it did reach this level for fluvoxamine or paroxetine until after 6 weeks.
Conclusions: The differential period of onset of action should help guide clinicians in determining a suitable duration of antidepressants for depression.
Copyright 2003 John Wiley & Sons, Ltd.
Similar articles
-
Differential effects of fluvoxamine, paroxetine and milnacipran for depression, especially with regard to age.Hum Psychopharmacol. 2004 Aug;19(6):405-8. doi: 10.1002/hup.608. Hum Psychopharmacol. 2004. PMID: 15303244 Clinical Trial.
-
Gender differences in the clinical effects of fluvoxamine and milnacipran in Japanese major depressive patients.Psychiatry Clin Neurosci. 2007 Aug;61(4):421-7. doi: 10.1111/j.1440-1819.2007.01679.x. Psychiatry Clin Neurosci. 2007. PMID: 17610668
-
Differential effects of milnacipran, fluvoxamine and paroxetine for depression, especially in gender.Eur Psychiatry. 2003 Dec;18(8):418-20. doi: 10.1016/j.eurpsy.2003.05.002. Eur Psychiatry. 2003. PMID: 14680720 No abstract available.
-
[Prediction of antidepressant response to milnacipran and fluvoxamine using pharmacogenetical methods].Nihon Shinkei Seishin Yakurigaku Zasshi. 2010 Apr;30(2):71-6. Nihon Shinkei Seishin Yakurigaku Zasshi. 2010. PMID: 20491280 Review. Japanese.
-
Milnacipran and selective serotonin reuptake inhibitors in major depression.Int Clin Psychopharmacol. 1996 Sep;11 Suppl 4:41-6. doi: 10.1097/00004850-199609004-00006. Int Clin Psychopharmacol. 1996. PMID: 8923126 Review.
Cited by
-
Chronic treatment with milnacipran reverses the impairment of synaptic plasticity induced by conditioned fear stress.Psychopharmacology (Berl). 2005 May;179(3):606-12. doi: 10.1007/s00213-004-2094-1. Epub 2004 Dec 24. Psychopharmacology (Berl). 2005. PMID: 15619117
-
Japanese experience with milnacipran, the first serotonin and norepinephrine reuptake inhibitor in Japan.Neuropsychiatr Dis Treat. 2007 Feb;3(1):41-58. doi: 10.2147/nedt.2007.3.1.41. Neuropsychiatr Dis Treat. 2007. PMID: 19300537 Free PMC article.
-
Remission rates with milnacipran 100 mg/day and 150 mg/day in the long-term treatment of major depression.Clin Drug Investig. 2006;26(3):135-42. doi: 10.2165/00044011-200626030-00003. Clin Drug Investig. 2006. PMID: 17163244
-
Long-lasting behavioral effects and recognition memory deficit induced by chronic mild stress in mice: effect of antidepressant treatment.Psychopharmacology (Berl). 2008 Jul;199(1):1-14. doi: 10.1007/s00213-007-1035-1. Epub 2008 May 10. Psychopharmacology (Berl). 2008. PMID: 18470507
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical