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Soma is a centrally-acting skeletal muscle relaxant. It is a colorless, crystalline powder, having a mild characteristic odor and a bitter taste. Soma is slightly soluble in water and freely soluble in alcohol, chloroform and acetone. The drug's solubility is practically independent of pH. Soma is manufactured and marketed in the United States by Meda Pharmaceuticals Inc. underneath the manufacturer name SOMA, and in the United Kingdom and other nations beneath the brand name names Sanoma and Carisoma. The medicine is attainable by itself or mixed with aspirin and in a single preparation (Soma Compound With Codeine) along with codeine and caffeine as good.

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However reports from Norway have shown that Soma has abuse possible as a buy dihydrocodeine 30mg online of meprobamate and/or potentiator of hydrocodone, dihydrocodeine, codeine and comparable medicines, it continues to be prescribed in North America, alongside orphenadrine and cyclobenzaprine. In Europe, medical doctors favor cyclobenzaprine. In the United Kingdom, benzodiazepines are preferred instead. All of the above plus chlorzoxazone are made use of in Canada.

As of November 2007, Soma (Somadril, Somadril comp.) has been taken off the industry in Sweden due to conditions with dependence and facet side effects. The agency overseeing pharmaceuticals has thought to be other pills applied with the similar indications as Soma to have the same exact or greater influences devoid of the dangers of the drug. In Will probably 2008 it was used off the market place in Norway as nicely.

In the EU, the European Medicines Agency has issued a release recommending that member states suspend marketing and advertising authorization for this device in the therapy of acute (not chronic) back soreness.

In the United States, even though Soma is not a contolled element under federal regulations, as of February 2010, Soma is thought to be to be a timetable IV managed element by the says of Alabama, Arizona, Arkansas, Florida, Georgia, Hawaii, Indiana, Kentucky, Louisiana, Massachusetts, Minnesota, Mississippi, New Mexico, Nevada, Oklahoma, Oregon and Texas (scheduled making use of the says new manipulated material software which calls for physicians to obtain, and include, a state "DPS" quantity as nicely as a DEA amount on all controlled ingredients prescriptions) and Washington State. It is a Program III manipulated element in West Virginia. The rest of the United States, excluding the above named states, falls below the DEA scheduling for the drug, which considers Soma a non-scheduled chemical, meaning that Soma is deemed a typical prescription medicine by the federal government of the United States, with oversight provided solely by the U.S. Food and Medication Administration (FDA). On March 26th, 2010 the DEA issued a Notice of hearing on proposed rule making in respect to the placement of Soma in timetable IV of the Managed Substances Act.