Pharmacotherapeutic profile of venlafaxine
- 1 January 1997
- journal article
- Published by Cambridge University Press (CUP) in European Psychiatry
- Vol. 12 (S4) , 285s-294s
- https://doi.org/10.1016/s0924-9338(97)83307-x
Abstract
When selecting an antidepressant, a number of factors must be considered. These considerations are summarized under the mnemonic STEPS: Safety, Tolerability, Efficacy, Payment (eg, cost-effectiveness), and Simplicity of use. Venlafaxine is the first of a new class of antidepressants that selectively blocks the serotonin and noradrenaline uptake pumps without blocking muscarinic, histaminergic and adrenergic receptors or inhibiting sodium fast channels. Because venlafaxine avoids these mechanisms of action, it has a wide therapeutic index, an improved tolerability profile and a reduced risk of causing pharmacodynamically mediated drug-drug interactions when compared to tricyclic antidepressants (TCAs). In contrast to some other new antidepressants, venlafaxine also avoids effects on cytochrome P450 which are likely to cause clinically meaningful, pharmacokinetically mediated drug-drug interactions. The effects on the uptake pumps of both serotonin and noradrenaline appear to be responsible for some of venlafaxine's unique features in terms of antidepressant efficacy, including its ascending antidepressant dose-response curve and its apparent rapid onset of antidepressant action at the upper end of its clinically relevant dosing range. Venlafaxine is effective in a broad spectrum of patients, including outpatients and inpatients, those with and without melancholia, patients with symptoms of anxiety or agitation or retardation and patients with first time or recurrent episodes of major depression. An important factor when selecting an antidepressant is the simplicity of the dosing regimen and the ability to rapidly and confidently achieve the optimal dose for the patient. In this regard, venlafaxine can be initiated at a clinically effective dose from the beginning. If the patient fails to respond to this dose, there is evidence that increased antidepressant efficacy can be achieved by increasing the dose rather than having to resort to an augmentation strategy or switch to another class of antidepressants. In the immediate release form, venlafaxine has proven antidepressant efficacy when using a twice-or three-times-a-day schedule. A sustained release formulation is expected to be marketed soon and will permit once-a-day-dosing.Keywords
This publication has 16 references indexed in Scilit:
- Treating Depression: Potential Drug InteractionsPsychiatric Annals, 1997
- Venlafaxine oxidationin vitrois catalysed by CYP2D6British Journal of Clinical Pharmacology, 1996
- A double-blind comparison of venlafaxine and fluoxetine for treatment of major depression in outpatientsProgress in Neuro-Psychopharmacology and Biological Psychiatry, 1996
- A double-blind comparison of venlafaxine and fluoxetine in patients hospitalized for major depression and melancholiaInternational Clinical Psychopharmacology, 1994
- Binding of antidepressants to human brain receptors: focus on newer generation compoundsPsychopharmacology, 1994
- Blockade by newly-developed antidepressants of biogenic amine uptake into rat brain synaptosomesLife Sciences, 1993
- A Preliminary, Open Study of the Combination of Fluoxetine and Desipramine for Rapid Treatment of Major DepressionArchives of General Psychiatry, 1991
- Biochemical, neurophysiological, and behavioral effects of Wy‐45,233 and other identified metabolites of the antidepressant venlafaxineDrug Development Research, 1991
- Rapid down regulation of β-adrenoceptors by co-administration of desipramine and fluoxetineEuropean Journal of Pharmacology, 1988
- Antidepressant biochemical profile of the novel bicyclic compound Wy-45,030, an ethyl cyclohexanol derivativeBiochemical Pharmacology, 1986