Literature DB >> 14716706

The treatment of depression with different formulations of venlafaxine: a comparative analysis.

James S Olver1, Graham D Burrows, Trevor R Norman.   

Abstract

Venlafaxine is the first of a group of antidepressants that show dual reuptake inhibition of serotonin and noradrenaline (SNRIs). Originally marketed in an immediate release (IR) formulation a microencapsulated, extended release (XR) formulation is now available. Significant differences exist between these two formulations with respect to pharmacokinetic parameters which have an impact on clinical use. The XR has lower maximum plasma concentrations (Cmax) and achieves these at a later time (higher Tmax). The longer apparent elimination half-life of the drug after single XR doses suggests that it is suitable for once daily dosing compared with the twice daily dosing regimen required by the IR formulation. With respect to antidepressant efficacy the XR formulation is equivalent to other marketed antidepressants and to the IR formulation. Consistent with its pharmacokinetic properties the use of the XR formulation is associated with less nausea and dizziness at the initiation of therapy. While in clinical usage XR might be expected to increase compliance with medication and to reduce discontinuation syndromes there are few comparative studies for which this has been evaluated. The XR formulation of venlafaxine is no worse than the IR form with respect to tolerability and offers some benefits to patients in terms of ease of use. On the other hand there does not appear to be any increase in the efficacy of the active agent. Copyright 2004 John Wiley & Sons, Ltd.

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Year:  2004        PMID: 14716706     DOI: 10.1002/hup.551

Source DB:  PubMed          Journal:  Hum Psychopharmacol        ISSN: 0885-6222            Impact factor:   1.672


  7 in total

1.  Fabrication of triple-layer matrix tablets of venlafaxine hydrochloride using xanthan gum.

Authors:  Mukesh C Gohel; Shital H Bariya
Journal:  AAPS PharmSciTech       Date:  2009-05-15       Impact factor: 3.246

2.  Gene-class analysis of expression patterns induced by psychoactive pharmaceutical exposure in fathead minnow (Pimephales promelas) indicates induction of neuronal systems.

Authors:  Michael A Thomas; Parag P Joshi; Rebecca D Klaper
Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2011-06-06       Impact factor: 3.228

3.  Differential outcomes from metabolic ratios in the identification of CYP2D6 phenotypes--focus on venlafaxine and O-desmethylvenlafaxine.

Authors:  Mani Kandasamy; P Srinivas; Kala Subramaniam; Sandhya Ravi; James John; Radha Shekar; Nuggehally Srinivas; Saral Thangam
Journal:  Eur J Clin Pharmacol       Date:  2010-05-06       Impact factor: 2.953

4.  Serotonin norepinephrine reuptake inhibitors: a pharmacological comparison.

Authors:  Randy A Sansone; Lori A Sansone
Journal:  Innov Clin Neurosci       Date:  2014-03

5.  The effect of the antidepressant venlafaxine on gene expression of biotransformation enzymes in zebrafish (Danio rerio) embryos.

Authors:  Nikola Hodkovicova; Pavla Sehonova; Jana Blahova; Martin Faldyna; Petr Marsalek; Premysl Mikula; Petr Chloupek; Radka Dobsikova; Vladimir Vecerek; Monika Vicenova; Petra Vosmerova; Zdenka Svobodova
Journal:  Environ Sci Pollut Res Int       Date:  2019-11-21       Impact factor: 4.223

6.  Psychoactive pharmaceuticals induce fish gene expression profiles associated with human idiopathic autism.

Authors:  Michael A Thomas; Rebecca D Klaper
Journal:  PLoS One       Date:  2012-06-06       Impact factor: 3.240

7.  Impact of iron fortification on anaemia and iron deficiency among pre-school children living in Rural Ghana.

Authors:  Samuel Kofi Tchum; Fareed Kow Arthur; Bright Adu; Samuel Asamoah Sakyi; Latifatu Alhassan Abubakar; Dorcas Atibilla; Seeba Amenga-Etego; Felix Boakye Oppong; Francis Dzabeng; Benjamin Amoani; Thomas Gyan; Emmanuel Arhin; Kwaku Poku-Asante
Journal:  PLoS One       Date:  2021-02-11       Impact factor: 3.240

  7 in total

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