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FDA Approves Ampyra to Improve Walking in Adults with Multiple Sclerosis
Date:1/23/2010

clinical trials include urinary tract infection, insomnia, dizziness, headache, nausea, weakness, back pain, balance disorder, swelling in the nose or throat, constipation, diarrhea, indigestion, throat pain, and burning, tingling or itching of skin.

Ampyra should not be used in patients with moderate to severe kidney disease. In these patients, blood levels with the drug approach those associated with the occurrence of seizures.

Ampyra will be manufactured under licenses from Elan of Dublin, Ireland, and distributed by Acorda Therapeutics Inc. of Hawthorne, N.Y.

For information about FDA drug approvals: http://www.fda.gov/Drugs/default.htm.

Contact: Sandy Walsh, 301-796-4669, sandy.walsh@fda.hhs.gov

SOURCE U.S. Food and Drug Administration

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