Literature DB >> 11893234

Paroxetine: an update of its use 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: 11893234     DOI: 10.2165/00003495-200262040-00010

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


  140 in total

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Authors:  G Perna; A Bertani; D Caldirola; E Smeraldi; L Bellodi
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Authors:  D Baldwin; J Bobes; D J Stein; I Scharwächter; M Faure
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3.  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

4.  Treatment discontinuation with selective serotonin reuptake inhibitors compared with tricyclic antidepressants: a meta-analysis.

Authors:  I M Anderson; B M Tomenson
Journal:  BMJ       Date:  1995-06-03

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

Review 7.  Panic disorder: the place of benzodiazepines and selective serotonin reuptake inhibitors.

Authors:  S Kasper; E Resinger
Journal:  Eur Neuropsychopharmacol       Date:  2001-08       Impact factor: 4.600

8.  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

9.  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

10.  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
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1.  Exposure to oral oxycodone is increased by concomitant inhibition of CYP2D6 and 3A4 pathways, but not by inhibition of CYP2D6 alone.

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2.  Paroxetine for somatic pain associated with physical illness: a review.

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3.  Pharmacological Management of Anxiety Disorders in the Elderly.

Authors:  Elizabeth A Crocco; Sindy Jaramillo; Caroline Cruz-Ortiz; Katherine Camfield
Journal:  Curr Treat Options Psychiatry       Date:  2017-02-10

4.  Paroxetine: population pharmacokinetic analysis in late-life depression using sparse concentration sampling.

Authors:  Yan Feng; Bruce G Pollock; Robert E Ferrell; Mark A Kimak; Charles F Reynolds; Robert R Bies
Journal:  Br J Clin Pharmacol       Date:  2006-05       Impact factor: 4.335

5.  Slow versus standard up-titration of paroxetine for the treatment of depression in cancer patients: a pilot study.

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Review 6.  Paroxetine controlled release.

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

7.  A prospective examination of antidepressant use and its correlates in patients with acute coronary syndrome.

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8.  Acid sensing ion channel (ASIC) inhibitors exhibit anxiolytic-like activity in preclinical pharmacological models.

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9.  Dual modes of extracellular serotonin changes in the rat ventral striatum modulate adaptation to a social stress environment, studied with wireless voltammetry.

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10.  Single point activation of pyridines enables reductive hydroxymethylation.

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