Literature DB >> 9463792

Paroxetine. An update of its pharmacology and therapeutic use in depression and a review of its use in other disorders.

N S Gunasekara1, S Noble, P Benfield.   

Abstract

Paroxetine is a potent and selective inhibitor of the neuronal reuptake of serotonin (5-hydroxytryptamine; 5-HT), which was previously reviewed as an antidepressant in Drugs in 1991. Since then, more comparative trials with other antidepressants have become available, and its use in the elderly and as long term maintenance therapy has been investigated. Paroxetine has also been studied in several other disorders with a presumed serotonergic component, primarily obsessive compulsive disorder (OCD) and panic disorder. In short term clinical trials in patients with depression, paroxetine produced clinical improvements that were significantly greater than those with placebo and similar to those achieved with other agents including tricyclic antidepressants (TCAs), maprotiline, nefazodone and the selective serotonin reuptake inhibitors (SSRIs) fluoxetine, fluvoxamine and sertraline. Long term data suggest that paroxetine is effective in preventing relapse or recurrence of depression in patients treated for up to 1 year. In the elderly, the overall efficacy of paroxetine was at least as good as that of comparator agents. In short term clinical trials involving patients with OCD or panic disorder, paroxetine was significantly more effective than placebo and of similar efficacy to clomipramine. Limited long term data show that paroxetine is effective in maintaining a therapeutic response over periods of 1 year (OCD) and up to 6 months (panic disorder). Preliminary data suggest that paroxetine has potential in the treatment of social phobia, premenstrual dysphoric disorder and chronic headache. Like the other SSRIs, paroxetine is better tolerated than the TCAs, causing few anticholinergic adverse effects. The most commonly reported adverse event associated with paroxetine treatment is nausea, although this is generally mild and subsides with continued use. Fewer withdrawals from treatment due to adverse effects occurred with paroxetine treatment than with TCAs. The adverse events profile of paroxetine appears to be broadly similar to that of other SSRIs, although data from comparative trials are limited. Serious adverse effects associated with paroxetine are very rare. In conclusion, paroxetine is effective and well tolerated, and suitable as first-line therapy for depression. It also appears to be a useful alternative to other available agents for the treatment of patients with OCD or panic disorder.

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Year:  1998        PMID: 9463792     DOI: 10.2165/00003495-199855010-00007

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  123 in total

1.  Evaluation of the potential for interactions of paroxetine with diazepam, cimetidine, warfarin, and digoxin.

Authors:  S J Bannister; V P Houser; J D Hulse; J C Kisicki; J G Rasmussen
Journal:  Acta Psychiatr Scand Suppl       Date:  1989

2.  The pharmacokinetics of paroxetine in the elderly.

Authors:  A J Bayer; N A Roberts; E A Allen; M Horan; P A Routledge; C G Swift; M M Byrne; A Clarkson; B D Zussman
Journal:  Acta Psychiatr Scand Suppl       Date:  1989

3.  A double-blind, multicentre study of paroxetine and maprotiline in major depression.

Authors:  U Schnyder; A Koller-Leiser
Journal:  Can J Psychiatry       Date:  1996-05       Impact factor: 4.356

4.  Dose-dependent inhibition of CYP1A2, CYP2C19 and CYP2D6 by citalopram, fluoxetine, fluvoxamine and paroxetine.

Authors:  U Jeppesen; L F Gram; K Vistisen; S Loft; H E Poulsen; K Brøsen
Journal:  Eur J Clin Pharmacol       Date:  1996       Impact factor: 2.953

5.  Medication withdrawal symptoms in obsessive-compulsive disorder patients treated with paroxetine.

Authors:  N J Keuthen; P Cyr; J A Ricciardi; W E Minichiello; M L Buttolph; M A Jenike
Journal:  J Clin Psychopharmacol       Date:  1994-06       Impact factor: 3.153

6.  A comparison of paroxetine, clomipramine and placebo in the treatment of panic disorder. Collaborative Paroxetine Panic Study Investigators.

Authors:  Y Lecrubier; A Bakker; G Dunbar; R Judge
Journal:  Acta Psychiatr Scand       Date:  1997-02       Impact factor: 6.392

Review 7.  Nefazodone. A review of its pharmacology and clinical efficacy in the management of major depression.

Authors:  R Davis; R Whittington; H M Bryson
Journal:  Drugs       Date:  1997-04       Impact factor: 9.546

8.  Paroxetine versus placebo: a double-blind comparison in depressed patients.

Authors:  J L Claghorn; A Kiev; K Rickels; W T Smith; G C Dunbar
Journal:  J Clin Psychiatry       Date:  1992-12       Impact factor: 4.384

9.  Further evidence for the importance of 5-HT1A autoreceptors in the action of selective serotonin reuptake inhibitors.

Authors:  S Hjorth; S B Auerbach
Journal:  Eur J Pharmacol       Date:  1994-08-01       Impact factor: 4.432

10.  The safety of concomitant use of sumatriptan and antidepressant treatments.

Authors:  P Blier; R Bergeron
Journal:  J Clin Psychopharmacol       Date:  1995-04       Impact factor: 3.153

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  20 in total

Review 1.  The anti-inflammatory role of SSRI and SNRI in the treatment of depression: a review of human and rodent research studies.

Authors:  Vlad Dionisie; Gabriela Adriana Filip; Mihnea Costin Manea; Mirela Manea; Sorin Riga
Journal:  Inflammopharmacology       Date:  2020-11-08       Impact factor: 4.473

2.  Paroxetine suppresses reactive microglia-mediated but not lipopolysaccharide-induced inflammatory responses in primary astrocytes.

Authors:  Xiong Zhang; Lan-Bing Zhu; Jia-Hui He; Hong-Qiu Zhang; Shu-Ya Ji; Chao-Nan Zhang; Na-Na Hou; Chen-Ping Huang; Jian-Hong Zhu
Journal:  J Neuroinflammation       Date:  2020-02-05       Impact factor: 8.322

Review 3.  Effects of liver disease on pharmacokinetics. An update.

Authors:  V Rodighiero
Journal:  Clin Pharmacokinet       Date:  1999-11       Impact factor: 6.447

4.  Efficacy of prophylactic treatment with selective serotonin reuptake inhibitors for depression after open-heart surgery.

Authors:  Mitsumasa Hata; Yuko Yagi; Akira Sezai; Isamu Yoshitake; Shinji Wakui; Ayako Takasaka; Hideomi Kawachi; Tomohiko Murakami; Kazutomo Minami; Motomi Shiono
Journal:  Surg Today       Date:  2011-05-28       Impact factor: 2.549

Review 5.  Paroxetine: a review.

Authors:  M Bourin; P Chue; Y Guillon
Journal:  CNS Drug Rev       Date:  2001

Review 6.  Paroxetine controlled release.

Authors:  Lynne M Bang; Gillian M Keating
Journal:  CNS Drugs       Date:  2004       Impact factor: 5.749

7.  Rapid Construction of (-)-Paroxetine and (-)-Femoxetine via N-Heterocyclic Carbene Catalyzed Homoenolate Addition to Nitroalkenes.

Authors:  Nicholas A White; Kerem E Ozboya; Darrin M Flanigan; Tomislav Rovis
Journal:  Asian J Org Chem       Date:  2014-04       Impact factor: 3.319

8.  Polymorphism of human cytochrome P450 2D6 and its clinical significance: part II.

Authors:  Shu-Feng Zhou
Journal:  Clin Pharmacokinet       Date:  2009       Impact factor: 6.447

9.  A Proposed Algorithm for Improved Recognition and Treatment of the Depression/Anxiety Spectrum in Primary Care.

Authors:  James C. Ballenger; Jonathan R. T. Davidson; Yves Lecrubier; David J. Nutt
Journal:  Prim Care Companion J Clin Psychiatry       Date:  2001-04

Review 10.  Pharmacokinetics of antidepressants in patients with hepatic impairment.

Authors:  Massimo Carlo Mauri; Alessio Fiorentini; Silvia Paletta; Alfredo Carlo Altamura
Journal:  Clin Pharmacokinet       Date:  2014-12       Impact factor: 6.447

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