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Recent News and Articles on the Keywords: emsam + depression + transdermal  Related to the article below (Last Update: 12/1/2008)

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Recent News and Articles on the Keywords: depression + patch + emsam  Related to the article below (Last Update: 8/7/2008)

Mylan buys out Watson?s interest in Somerset Pharmaceuticals
Bizjournals.com, NC - Jul 29, 2008
Somerset developed Emsam, a transdermal patch for the treatment of depression. Emsam is marketed in the United States by New York-based Bristol-Myers Squibb ...
Business Briefs -- 07/30 Press-Enterprise
all 11 news articles »  MYL - WPI
Source: Google News

MAOI Skin Patch Wins FDA Approval for Depression -
J Rosack - Psychiatric News, 2006 - Am Psychiatric Assoc
... depression. The new skin patch, developed by Somerset Pharmaceuticals, will be marketed
in the US by Bristol-Myers Squibb Company under the brand name Emsam. ...

Selegiline Transdermal Patch (Emsam) for Major Depressive Disorder
B Line - aafp.org
... selegiline transdermal patch (Emsam) delivers higher, more sustained blood levels
to the brain and is labeled for the treatment of major depression in adults.1 ...

New MAOI transdermal patch available to treat major depressive disorder in adults
O daily EMSAM - The Brown University Geriatric Psychopharmacology Update, 2006 - doi.wiley.com
... Our top story this month focuses on the first-ever transdermal patch available to
treat major depression. EMSAM (selegiline) was just approved by the FDA and ...

[CITATION] US FDA Approves MAOI Patch to Treat Depression
DR Center

Transdermal Selegiline: New Opportunity for Managing Depression -
EH Tobe - JAOA: Journal of the American Osteopathic Association, 2008 - Am Osteopathic Assoc
... LETTER. Transdermal Selegiline: New Opportunity for Managing Depression. ... The selegiline
transdermal patch system (EMSAM?; Bristol-Myers Squibb Co ...
-

[PDF] … : Absorption: Approximately 25-30% of the selegiline content in the transdermal patch is delivered
P ACTION - dhmh.state.md.us
... Depression: Selegiline transdermal system (EMSAM) may extend therapeutic options
for prescribers of antidepressant medications. The patch provides a unique ...

[PDF] The First Transdermal Antidepressant
RX Primer - americanpsychotherapy.com
... for depression with atypical features 1 such as mood reactivity, increased appe-
tite, and weight gain. 2 In 2006 a trans- dermal MAOI selegiline patch (EMSAM) ...

FDA Approvals: Rituxan and Emsam CME/CE
L Disclaimer - medscape.com
... Transdermal System (Emsam) for Adults With Major Depression. ... the FDA approved selegiline
transdermal system (Emsam, made by ... release, it is the first patch to be ...

Transdermal Patch Could Herald Renewed Popularity for MAOIs -
J Rosack - Psychiatric News, 2002 - Am Psychiatric Assoc
... clinical trials involving the transdermal patch, was funded ... is developing the product
under the trade name EmSam. ... MD, director of the Depression Research Unit ...

Rhabdomyolysis and quetiapine-fluoxetine combination
BM Behavior, RI Providence - The Brown University Psychopharmacology Update, 2007 - doi.wiley.com
... oxidase inhibitor (MAOI), adminis- tered as a once-daily transdermal patch (EMSAM),
appears to be effective in reduc- ing moderate-to-severe depression and in ...

Source: Google Scholar
 
 

Emsam is the first transdermal patch for depression

The FDA ( U.S. Food and Drug Administration ) approved Emsam ( Selegiline ), the first transdermal patch for use in treating major depression.

The once a day patch works by delivering Selegiline, a monoamine oxidase inhibitor or MAOI, through the skin and into the bloodstream.
At its lowest strength, Emsam can be used without the dietary restrictions that are needed for all oral MAO inhibitors that are approved for treating major depression.

Major depressive disorder is a common psychiatric condition in the U.S. population.
Symptoms of depression include general emotional dejection, withdrawal and restlessness that interfere with daily functioning, such as loss of interest in usual activities; significant change in weight and/or appetite; insomnia; increased fatigue; feelings of guilt or worthlessness; slowed thinking or impaired concentration; and a suicide attempt or suicidal ideation.

MAO inhibitors usually require specific dietary restrictions because when combined with certain foods they can cause a sudden, large increase in blood pressure, or “hypertensive crisis”.
A hypertensive crisis can lead to a stroke and death.
Symptoms of a hypertensive crisis include sudden onset of severe headache, nausea, stiff neck, a fast heartbeat or a change in palpitations, sweating, and confusion.

. The lowest dose of the MAOI patch, which delivers 6 mg of the medication over a 24 hour period, can be used without such dietary restrictions.

The Emsam patch will be made available in three sizes that deliver 6, 9, or 12 mg of Selegiline per 24 hours.
The patch is a matrix containing three layers consisting of a backing, and adhesive drug layer, and a release liner that is placed against the skin.

Emsam has been shown safe and effective for treatment of major depressive disorder in two 6-8 week studies and also in a longer-term study of patients.
The data for EMSAM 6mg/24hr support the recommendation that a modified diet is not required at this dose.
Patients are advised to change the patch once a day.

The more limited data available for Emsam 9mg/24hr and 12mg/24hr do not rule out food effects so that patients receiving these higher doses should follow dietary restrictions that advise them to avoid certain foods or beverages. This includes foods and beverages such as aged cheese and wine.

The only common side effect of Emsam detected in placebo-controlled trials was a mild skin reaction where the patch is placed. There may be mild redness at the site when a patch is removed. If the redness does not go away within several hours after removing the patch or if irritation or itching continues, patients are advised to contact their doctor.

Another side effect that was seen less commonly was light-headedness related to a drop in blood pressure.

Source: FDA, 2006

 
 
 
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