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SOMA 250 MG Shown To Significantly Improve Functionality and Reduce Disability in Patients With Low Back Pain in Three Days
Date:2/3/2010

SOMERSET, N.J., Feb. 3 /PRNewswire/ -- A recent analysis of two pivotal clinical trials in patients with acute low back pain (ALBP) who were treated with SOMA® (carisoprodol) 250 mg showed significantly improved functionality and reduced disability after three days of treatment, as measured by the Roland-Morris Disability Questionnaire (RMDQ).  This analysis is being presented this week at the 26th annual meeting of the American Academy of Pain Medicine in San Antonio, TX.   In addition, a recent review of published literature indicates that SOMA 250 mg is the only skeletal muscle relaxant proven to significantly improve functionality in patients with acute low back pain as measured by the RMDQ.   SOMA 250 mg is indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions.

"This outcomes data differentiates SOMA 250 mg among the diverse treatment choices for patients with acute low back pain," said Steven M. Simon, MD, RPh, Clinical Assistant Professor, University of Kansas and Kansas City, University of Medicine and Biosciences. "Almost all acute low back pain is mechanical in origin and one in five patients with this condition suffers from significant limitations in activity.  Treatment of acute low back pain with SOMA 250 mg has been shown to improve functionality, as measured by an internationally validated tool, and it may be a useful treatment option for many patients suffering from this common condition."

Low back pain can be a disabling condition that affects patients' ability to function.  Patients with acute low back pain may walk more slowly, sleep less, avoid common activities, and stay home.  

Outcomes-based healthcare is a comprehe
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