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Duloxetine hydrochloride (trade name: Cymbalta/Yentreve) occurs as medically utilized drug that primarily targets major depressive disorders (MDD), pain related to diabetic peripheral neuropathy and stress urinary incontinence (SUI). Known too when LY248686, chemically (+)-(S)-North-methyl-Three-(One-naphthyloxy)-Two-thiophenepropanamine, these are the potent dual inhibitor of serotonin (Five-serotonin, 5-HT) & norepinephrine (NE) reuptake, possessing corresponding affinities around binding to NE & Five-HT conveyance web sites. Interestingly, its behavior contrasts to virtually all more dual-reuptake inhibitors.

Moreover, duloxentine lacks affinity for monoamine receptors within the central nervous system. When there exists limited information available on a pharmacokinetic profile of duloxetine in human being, its half-life is reported to be 10 to 15 hours.

Duloxentine is as well approved per FDA for the coarse of action of diabetic neuropathy.

APA: Duloxetine Has Little Effect on Body Weight
Report on research findings announced at meeting in May 2002.

Duloxetine for Major Depressive Disorder: A Randomized Double-Blind Placebo-Controlled Trial
Abstract of study findings published in April 2002.

Duloxetine: Lilly Receives Approvable Letter
News on FDA action in September 2002 related to the dual 5HT/noradrenaline reuptake inhibitor (also known as Cymbalta) for the treatment of depression.

Duloxetine Antidepressant Action Begins in One Week
Report on study findings announced in October 2002. [MedScape - Free registration required.]

Cymbalta
Manufacturer's site for this selective serotonin and norepinephrine reuptake inhibitor (SSNRI), approved in the US to treat diabetic peripheral neuropathic pain and major depression.

Cymbalta
Full prescribing information from RxList.


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