When was savella approved by the fda

Study 2 This three-month, double-blind, placebo-controlled, multicenter study enrolled adult patients years of age. In both studies, some patients who rated themselves as globally "much" or "very much" improved experienced a decrease in pain as early as the first week of treatment. Lundbeck Takeda Pharmaceuticals U. Savella milnacipran hydrochloride Profile. Currently Enrolling Trials Show More. General Information Savella milnacipran is a selective serotonin and norepinephrine reuptake inhibitor.

The two studies were double-blind, placebo-controlled, multicenter studies in adult patients years of age diagnosed with fibromyalgia. The first study was six months long and the second was three months long. In addition, more patients treated with Savella as compared with placebo met the criteria for a treatment response as measured by concurrent improvements in pain, physical function, and patient global assessment.

The exact mechanism by which Savella improves the symptoms of fibromyalgia is unknown. However, some researchers believe that abnormalities in certain brain chemicals may be central to fibromyalgia, and that Savella blocks the reuptake of both norepinephrine and serotonin. These brain chemicals appear to play an important role in pain perception and sensitivity. Milnacipran Savella , a treatment option for fibromyalgia. Savella prescribing Information. Published January 8, Your Privacy Rights.

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