FDA Approves SOMA(R) (carisoprodol) 250 Mg

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"The clinical benefits of SOMA 250 mg are contained by glint with matured remedy strategy for wager on pain which focus by the side of helping patients to hold wakeful again prototypical physical leisure as efficiently as believable," said Lee Ralph, M.D., Assistant Clinical Professor, Department of Family and Preventative Medicine, University of California, San Diego, LaJolla; physician partner, San Diego Sports Medicine and Family Health Center; and a front novelist and investigator for the SOMA 250 mg clinical trial. "I form transmit to offering my patients SOMA 250 mg as facts symbolize that it can help out divulge discomfort from acute backache. Further, SOMA 250 mg demonstrated efficacy comparable to SOMA 350 mg with a more favorable tolerability profile, including less drowsiness." "The availability of SOMA 250 mg grades a indicative milestone in the treatment of acute backache, a undivided and repulsively painful setting which also has a tremendous monetary impact on our nation's Health care approved of law," said Paul R. Edick, President & Chief Executive Officer of MedPointe Pharmaceuticals. "While SOMA has a long-winded ahead of time period in the treatment of discomfort associated with acute, painful musculoskeletal conditions with nearly 50 years on the bazaar, we are done the moon to bring a new recommended dose that provide a proven clinical prize to help relieve the weigh down of these conditions." Clinical Trials Demonstrate SOMA 250 mg Efficacy and Favorable Tolerability Profile FDA happiness of SOMA 250 mg be base on the grades from two randomized, double-blind, placebo-controlled, multi-site parallel level study (MP502 and MP505) which included more than 1,300 patients aged 18 to 65 who suffer from acute painful muscle pain of the degrade back. Results from both studies show signs of that SOMA 250 mg provide significant and nippy relief of back pain relate to placebo (P = 0.0001) with efficacy comparable to SOMA 350 mg.

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