Literature DB >> 12027788

Spotlight on paroxetine in psychiatric disorders in adults.

Antona J Wagstaff1, Susan M Cheer, Anna J Matheson, Douglas Ormrod, Karen L Goa.   

Abstract

Paroxetine is a selective serotonin reuptake inhibitor (SSRI), with antidepressant and anxiolytic activity. In 6- to 24-week well designed trials, oral paroxetine 10 to 50 mg/day was significantly more effective than placebo, at least as effective as tricyclic antidepressants (TCAs) and as effective as other SSRIs and other antidepressants in the treatment of major depressive disorder. Relapse or recurrence over 1 year after the initial response was significantly lower with paroxetine 10 to 50 mg/day than with placebo and similar to that with imipramine 50 to 275 mg/day. The efficacy of paroxetine 10 to 40 mg/day was similar to that of TCAs and fluoxetine 20 to 60 mg/day in 6- to 12-week trials in patients aged > or = 60 years with major depression. Paroxetine 10 to 40 mg/day improved depressive symptoms to an extent similar to that of TCAs in patients with comorbid illness, and was more effective than placebo in the treatment of dysthymia and minor depression. Paroxetine 20 to 60 mg/day was more effective than placebo after 8 to 12 weeks' treatment of obsessive-compulsive disorder (OCD), panic disorder, social anxiety disorder (social phobia), generalised anxiety disorder (GAD) and post-traumatic stress disorder (PTSD). Improvement was maintained or relapse was prevented for 24 weeks to 1 year in patients with OCD, panic disorder, social anxiety disorder or GAD. The efficacy of paroxetine was similar to that of other SSRIs in patients with OCD and panic disorder and similar to that of imipramine but greater than that of 2'chlordesmethyldiazepam in patients with GAD. Paroxetine is generally well tolerated in adults, elderly individuals and patients with comorbid illness, with a tolerability profile similar to that of other SSRIs. The most common adverse events with paroxetine were nausea, sexual dysfunction, somnolence, asthenia, headache, constipation, dizziness, sweating, tremor and decreased appetite. In conclusion, paroxetine, in common with other SSRIs, is generally better tolerated than TCAs and is a first-line treatment option for major depressive disorder, dysthymia or minor depression. Like other SSRIs, paroxetine is also an appropriate first-line therapy for OCD, panic disorder, social anxiety disorder, GAD and PTSD. Notably, paroxetine is the only SSRI currently approved for the treatment of social anxiety disorder and GAD, which makes it the only drug of its class indicated for all five anxiety disorders in addition to major depressive disorder. Thus, given the high degree of psychiatric comorbidity of depression and anxiety, paroxetine is an important first-line option for the treatment of major depressive disorder, OCD, panic disorder, social anxiety disorder, GAD and PTSD.

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Year:  2002        PMID: 12027788     DOI: 10.2165/00023210-200216060-00006

Source DB:  PubMed          Journal:  CNS Drugs        ISSN: 1172-7047            Impact factor:   5.749


  75 in total

1.  A comparison of citalopram and paroxetine in the treatment of panic disorder: a randomized, single-blind study.

Authors:  G Perna; A Bertani; D Caldirola; E Smeraldi; L Bellodi
Journal:  Pharmacopsychiatry       Date:  2001-05       Impact factor: 5.788

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.  Paroxetine in social phobia/social anxiety disorder. Randomised, double-blind, placebo-controlled study. Paroxetine Study Group.

Authors:  D Baldwin; J Bobes; D J Stein; I Scharwächter; M Faure
Journal:  Br J Psychiatry       Date:  1999-08       Impact factor: 9.319

4.  Paroxetine and amitriptyline augmentation of lithium in the treatment of major depression: a double-blind study.

Authors:  M Bauer; R Zaninelli; B Müller-Oerlinghausen; W Meister
Journal:  J Clin Psychopharmacol       Date:  1999-04       Impact factor: 3.153

5.  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

6.  Efficacy of fluvoxamine, paroxetine, and citalopram in the treatment of obsessive-compulsive disorder: a single-blind study.

Authors:  E Mundo; L Bianchi; L Bellodi
Journal:  J Clin Psychopharmacol       Date:  1997-08       Impact factor: 3.153

7.  Randomized, placebo-controlled trial of paroxetine versus imipramine in depressed HIV-positive outpatients.

Authors:  A J Elliott; K K Uldall; K Bergam; J Russo; K Claypoole; P P Roy-Byrne
Journal:  Am J Psychiatry       Date:  1998-03       Impact factor: 18.112

8.  Treatment of depression in patients with breast cancer: a comparison between paroxetine and amitriptyline.

Authors:  G Pezzella; R Moslinger-Gehmayr; A Contu
Journal:  Breast Cancer Res Treat       Date:  2001-11       Impact factor: 4.872

9.  Effect of pindolol on onset of action of paroxetine in the treatment of major depression: intermediate analysis of a double-blind, placebo-controlled trial. Réseau de Recherche et d'Expérimentation Psychopharmacologique.

Authors:  R Bordet; P Thomas; B Dupuis
Journal:  Am J Psychiatry       Date:  1998-10       Impact factor: 18.112

10.  Paroxetine in the treatment of depression. A double-blind multicenter study versus mianserin.

Authors:  C Mertens; H Pintens
Journal:  Acta Psychiatr Scand       Date:  1988-06       Impact factor: 6.392

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  5 in total

1.  Research on the Development of Theme Trends and Changes of Knowledge Structures of Drug Therapy Studies on Major Depressive Disorder Since the 21st Century: A Bibliometric Analysis.

Authors:  Li Duan; Yunfeng Gao; Xiaojun Shao; ChunSheng Tian; Chunfeng Fu; Gang Zhu
Journal:  Front Psychiatry       Date:  2020-07-10       Impact factor: 4.157

2.  Prophylactic treatment with paroxetine ameliorates behavioral deficits and retards the development of amyloid and tau pathologies in 3xTgAD mice.

Authors:  Rhonda L Nelson; Zhihong Guo; Veerendra Madala Halagappa; Michelle Pearson; Audrey J Gray; Yasuji Matsuoka; Martin Brown; Bronwen Martin; Titilola Iyun; Stuart Maudsley; Robert F Clark; Mark P Mattson
Journal:  Exp Neurol       Date:  2007-02-13       Impact factor: 5.330

3.  Serotonin contracts the rat mesenteric artery by inhibiting 4-aminopyridine-sensitive Kv channels via the 5-HT2A receptor and Src tyrosine kinase.

Authors:  Dong Jun Sung; Hyun Ju Noh; Jae Gon Kim; Sang Woong Park; Bokyung Kim; Hana Cho; Young Min Bae
Journal:  Exp Mol Med       Date:  2013-12-13       Impact factor: 8.718

4.  Long-term consequences of chronic fluoxetine exposure on the expression of myelination-related genes in the rat hippocampus.

Authors:  Y Kroeze; D Peeters; F Boulle; J L Pawluski; D L A van den Hove; H van Bokhoven; H Zhou; J R Homberg
Journal:  Transl Psychiatry       Date:  2015-09-22       Impact factor: 6.222

5.  The influence of paroxetine on the pharmacokinetics of atomoxetine and its main metabolite.

Authors:  Ioana Todor; Adina Popa; Maria Neag; Dana Muntean; Corina Bocsan; Anca Buzoianu; Laurian Vlase; Ana-Maria Gheldiu; Ruxandra Chira; Corina Briciu
Journal:  Clujul Med       Date:  2015-11-15
  5 in total

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