Image:Lexapro logo.pngescitalopram (free base) structure
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Lexapro

Escitalopram is a medication developed by the Danish pharmaceutical company Lundbeck, that acts as a selective serotonin reuptake inhibitor or SSRI. It is typically used as an antidepressant to treat depression associated with mood disorders although also may be used in the treatment of body dysmorphic disorder and anxiety. In the United States, the drug is marketed under the name Lexapro® by Forest Laboratories, Inc. In Canada and Europe, the drug is marketed under the name Cipralex® by Lundbeck Canada, Inc. more...

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Escitalopram oxalate is derived from the drug citalopram which is made up of two mirror-image isomers, only one of which is thought to be an effective medication. Lundbeck has split the isomers apart, taken the active isomer and has licensed it as the new drug escitalopram. Escitalopram is the pure S-enantiomer (single isomer) of the racemic bicyclic phthalane derivative citalopram.

Escitalopram was released shortly before the patent for citalopram was due to expire. The expiration of a patent means other companies can legally produce cheaper generic versions. Escitalopram is subject to a new patent. Critics have argued that escitalopram, and the subsequent marketing campaign to persuade mental health professionals to prescribe it, is a cynical ploy to promote sales of a virtually identical but considerably more expensive drug. In defence of the new drug, Lundbeck has claimed that the drug has additional benefits over the older citalopram and other antidepressant drugs on the market, mainly better tolerability .

Withdrawal symptoms

A possible withdrawal symptom from Escitalopram is a type of spontaneous nerve pulse, described by some patients as a feeling of small electric shocks, which may be accompanied by dizziness. These pulses may be short in duration, only milliseconds long, affect any region of the body, and recur up to several times a minute, throughout all waking hours. They can be increased by physical activity, but are not solely linked to muscular activity.

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Generalized anxiety disorder: study shows Lexapro better tolerated than Paxil
From OB/GYN News, 7/15/04 by Damian McNamara

MIAMI -- Escitalopram is as effective as paroxetine, but is better tolerated, for long-term treatment of generalized anxiety disorder, Dr. Robert J. Bielski said at the annual conference of the Anxiety Disorders Association of America.

Selective serotonin reuptake inhibitors (SSRIs) are increasingly being prescribed for generalized anxiety disorder, according to Dr. Bielski, a researcher at Summit Research Network in Okemos, Mich., which conducts clinical trials for pharmaceutical companies, including Forest Labs Inc., the maker of escitalopram (Lexapro).

In a rare direct comparison, he and his colleagues assessed the efficacy and tolerability of escitalopram and paroxetine (Paxil), two agents approved by the Food and Drug Administration for treating generalized anxiety disorder. (Extended-release venlafaxine is also FDA approved for this condition.)

All participants met the DSM-IV definition for generalized anxiety disorder: a baseline score on the Hamilton Anxiety Scale of 18 or more. Mean age was 37 years. There were 60 patients randomized to escitalopram and 61 to paroxetine. The study began with a week of single-blind placebo treatment, followed by 24 weeks of double-blind, flexible-dose treatment with either 10-20 mg/day of escitalopram or 20-50 mg/day of paroxetine. After an additional 2 weeks to titrate participants down, their Hamilton anxiety scores were compared for mean change from baseline.

Efficacy was similar; both agents improved anxiety symptoms. The mean baseline Hamilton anxiety score was 23.7 in the escitalopram group and 23.4 in the paroxetine group. At the end of the study, the mean reduction in scores was 15.3 in the escitalopram group and 13.3 in the paroxetine group.

"The SSRIs are a family of antidepressants that are really revolutionary. They are so much better tolerated than their predecessors," Dr. Bielski said at the meeting.

A representative of GlaxoSmithKline, the maker of paroxetine, declined to comment on the findings.

There were differences in adverse effects between the two treatment groups. The researchers noted the most frequent adverse events in 10% or more of patients. In the escitalopram group, diarrhea (21%), upper respiratory tract infection (15%), and fatigue (12%) were most common. In the paroxetine group, ejaculation disorder (30%), anorgasmia (26%), and insomnia (26%) were most common.

There was a statistically significant difference in the numbers of patients who withdrew from the study because of adverse events, Dr. Bielski said. A total of 6.6% withdrew from the escitalopram group, compared with 22.6% of the paroxetine group.

Forest Labs Inc. is considering future studies to assess these findings, he said.

BY DAMIAN MCNAMARA

Miami Bureau

COPYRIGHT 2004 International Medical News Group
COPYRIGHT 2004 Gale Group

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