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Levacetylmethadol
Levacetylmethadol (INN), levomethadyl acetate (USAN), OrLAAM (trade name) or levo-α-acetylmethadol (LAAM)〔US Patent 2565592〕 is a synthetic opioid similar in structure to methadone. It has a long duration of action due to its active metabolites. It was approved in 1993 by the U.S. Food and Drug Administration for use in the treatment of opioid dependence. In 2001, Orlaam was removed from the European market due to reports of life-threatening ventricular rhythm disorders.〔(EMEA public statement on levoacethylmethadol ), link is broken〕 In 2003, Roxane Laboratories, Inc. discontinued Orlaam in the US.〔(U. S. FDA: Drug Shortages )〕
==Indications==
LAAM is indicated as a second-line treatment for the treatment and management of opioid dependence if patients fail to respond to drugs like methadone or buprenorphine. Before August 1993, LAAM was classified as a schedule I drug in the United States. LAAM is not approved for use in Australia and Canada. At present, it is a Schedule II Narcotic controlled substance in the United States with a DEA ACSCN of 9648 and a national aggregate annual manufacturing quota of 4 grammes as of 2013.
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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