Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2005;65(16):2379-404.
doi: 10.2165/00003495-200565160-00013.

Escitalopram: a review of its use in the management of major depressive disorder

Affiliations
Review

Escitalopram: a review of its use in the management of major depressive disorder

David Murdoch et al. Drugs. 2005.

Abstract

Escitalopram (Cipralex, Lexapro), the active S-enantiomer of the racemic selective serotonin reuptake inhibitor (SSRI) citalopram (RS-citalopram), is a highly selective inhibitor of the serotonin transporter protein. It possesses a rapid onset of antidepressant activity, and is an effective and generally well tolerated treatment for moderate-to-severe major depressive disorder (MDD). Pooled analyses from an extensive clinical trial database suggest that escitalopram is consistently more effective than citalopram in moderate-to-severe MDD. Preliminary studies suggest that escitalopram is as effective as other SSRIs and the extended-release (XR) formulation of the serotonin/noradrenaline (norepinephrine) reuptake inhibitor venlafaxine, and may have cost-effectiveness and cost-utility advantages. However, additional longer-term, comparative studies evaluating specific efficacy, tolerability, health-related quality of life and economic indices would be helpful in definitively positioning escitalopram relative to these other agents in the treatment of MDD. Nevertheless, available clinical and pharmacoeconomic data indicate that escitalopram is an effective first-line option in the management of patients with MDD.

PubMed Disclaimer

References

    1. Curr Med Res Opin. 2004 Jun;20(6):869-78 - PubMed
    1. CNS Drugs. 2004;18(13):911-32 - PubMed
    1. J Clin Pharmacol. 2005 Dec;45(12):1400-6 - PubMed
    1. Pharmacoeconomics. 2003;21(16):1185-209 - PubMed
    1. Indian J Psychiatry. 2004 Oct;46(4):333-41 - PubMed

MeSH terms

LinkOut - more resources