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SHORT REPORTS

First case report of recreational use of 2,5-dimethoxy-4-chloroamphetamine confirmed by toxicological screening

Ovaska, Hannaa; Viljoen, Adieb; Puchnarewicz, Malgorzatac; Button, Jennyc; Ramsey, Johnd; Holt, David W.e; Dargan, Paul I.a; Wood, David M.a

Author Information

aDepartment of Clinical Toxicology, Guy's and St Thomas' Poisons Unit, Guy's and St Thomas' NHS Foundation Trust, London

bDepartment of Chemical Pathology, Lister Hospital, Stevenage

Departments ofcForensic Toxicology Service

dBioanalytics, Analytical Unit

eTICTAC Communications Ltd, St George's University of London, London, UK

Correspondence to Dr Hanna Ovaska, MD, Specialist Registrar in General Medicine and Clinical Pharmacology and Therapeutics, Guy's and St Thomas' Poisons Unit, Avonley Road, London SE14 5ER, UK

Tel: +44 207 771 5315; fax: +44 207 771 5306;

e-mail:[email protected]

Received 13 December 2007 Accepted 9 February 2008

European Journal of Emergency Medicine15(6):p 354-356, December 2008. |DOI:10.1097/MEJ.0b013e3282fc765b

Abstract

Routine toxicological screening is generally not undertaken in patients with recreational drug toxicity. We report here the benefits of toxicological screening in confirming drugs that have been ingested and potentially detecting drugs that have not previously been reported in the medical literature. In this case, the patient was reported to have ingested a combination of 2,5-dimethoxy-4-iodoamphetamine and methylenedioxymetamphetamine and developed sympathomimetic toxicity, but on extended toxicological screening he was shown to have actually ingested 2,5-dimethoxy-4-chloroamphetamine and methylenedioxymetamphetamine. As 2,5-dimethoxy-4-chloroamphetamine is a substituted amphetamine, it is covered under the generic Misuse of Drugs act (1971) in the UK; although in the majority of the EU it remains uncontrolled, as there is no similar generic drug legislation. We believe that discrepancies in the legal status of recreational drugs in the EU limit the effectiveness of drug enforcement policies and that EU drug legislation should be harmonized to ensure consistency.

© 2008 Lippincott Williams & Wilkins, Inc.

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