Literature DB >> 17568687

The selegiline transdermal system in major depressive disorder: a systematic review of safety and tolerability.

Donald S Robinson1, Jay D Amsterdam.   

Abstract

BACKGROUND: Monoamine oxidase inhibitors (MAOIs) are highly efficacious antidepressants, but safety concerns have limited their broad use.
METHODS: We reviewed key safety and tolerability data from all clinical trials of patients with major depressive disorder (MDD) accrued during the clinical development of the selegiline transdermal system (STS), as reported to the Food and Drug Administration. This review includes data from both controlled and uncontrolled clinical trials involving STS-treated (n=2036) and placebo-treated (n=668) patients.
RESULTS: Except for the initial trial, subsequent trials, which involved STS doses ranging from 3 mg/24 h to 12 mg/24 h, lacked tyramine restrictions, and no acute hypertensive reactions occurred during study treatment. Safety experience with STS 6 mg/24 h supports this therapeutic dose without tyramine dietary modifications, but until more data are available for STS doses 9 mg/24 h and 12 mg/24 h, foods that are rich sources of tyramine should be avoided. The principal side effects of STS therapy were local dermal reactions and insomnia, both of which were dose-related. Side effects associated with MAOI treatment, such as sexual dysfunction and excessive weight gain, were uncommon.
CONCLUSIONS: A comprehensive review of safety from the clinical development program suggests that the STS is safe and well tolerated, with an improved safety margin compared with orally administered MAOIs.

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Year:  2007        PMID: 17568687     DOI: 10.1016/j.jad.2007.04.024

Source DB:  PubMed          Journal:  J Affect Disord        ISSN: 0165-0327            Impact factor:   4.839


  9 in total

1.  Combining Stimulants and Monoamine Oxidase Inhibitors: A Reexamination of the Literature and a Report of a New Treatment Combination.

Authors:  Joshua A Israel
Journal:  Prim Care Companion CNS Disord       Date:  2015-12-10

2.  Revisiting the effectiveness of standard antidepressants in bipolar disorder: are monoamine oxidase inhibitors superior?

Authors:  Alan G Mallinger; Ellen Frank; Michael E Thase; Michelle M Barwell; Nancy Diazgranados; David A Luckenbaugh; David J Kupfer
Journal:  Psychopharmacol Bull       Date:  2009

3.  Comparative neuroprotective effects of rasagiline and aminoindan with selegiline on dexamethasone-induced brain cell apoptosis.

Authors:  Shawna Tazik; Shakevia Johnson; Deyin Lu; Chandra Johnson; Moussa B H Youdim; Craig A Stockmeier; Xiao-Ming Ou
Journal:  Neurotox Res       Date:  2009-02-28       Impact factor: 3.911

Review 4.  Use of transdermal drug formulations in the elderly.

Authors:  Laure-Zoé Kaestli; Anne-Florence Wasilewski-Rasca; Pascal Bonnabry; Nicole Vogt-Ferrier
Journal:  Drugs Aging       Date:  2008       Impact factor: 3.923

5.  Reducing the Burden of Difficult-to-Treat Major Depressive Disorder: Revisiting Monoamine Oxidase Inhibitor Therapy.

Authors:  Larry Culpepper
Journal:  Prim Care Companion CNS Disord       Date:  2013-10-31

6.  Transdermal patches: the emerging mode of drug delivery system in psychiatry.

Authors:  Miriam Isaac; Carl Holvey
Journal:  Ther Adv Psychopharmacol       Date:  2012-12

7.  Glyceraldehyde-3-phosphate dehydrogenase-monoamine oxidase B-mediated cell death-induced by ethanol is prevented by rasagiline and 1-R-aminoindan.

Authors:  Xiao-Ming Ou; Deyin Lu; Chandra Johnson; Kevin Chen; Moussa B H Youdim; Grazyna Rajkowska; Jean C Shih
Journal:  Neurotox Res       Date:  2009-05-28       Impact factor: 3.911

8.  MAO-inhibitors in Parkinson's Disease.

Authors:  Peter Riederer; Gerd Laux
Journal:  Exp Neurobiol       Date:  2011-03-31       Impact factor: 3.261

Review 9.  EMSAM (deprenyl patch): how a promising antidepressant was underutilized.

Authors:  Gregory M Asnis; Margaret A Henderson
Journal:  Neuropsychiatr Dis Treat       Date:  2014-10-06       Impact factor: 2.570

  9 in total

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