On 25 March, the EMCDDA and Europol submitted a joint report on mephedrone to the Council of the EU, the European Commission and the European Medicines Agency (EMA), presenting a case for a formal risk assessment of the drug (1). Submission of this report concludes the first phase of Europe’s three-step process to monitor new drugs: (i) information exchange/early-warning; (ii) risk assessment; and (iii) decision-making/control (2). On the basis of this report, the Council and the Commission will decide in the coming weeks whether or not to launch a formal risk assessment of the substance.
Mephedrone was first notified to the agencies via the EU early-warning system in March 2008, triggering an EMCDDA–Europol information exchange on the substance. Towards the end of 2009, increased evidence of mephedrone use and availability in some European countries prompted the agencies in January 2010 to embark on a formal data-collection exercise on the drug, resulting in this report. The report features: the chemical and physical description of the drug; first indications of health and social risks; evidence of intoxications and fatalities; data on seizures; and available information on international trafficking and the involvement of organised crime.
Mephedrone is a central nervous system stimulant belonging to the group of synthetic cathinone derivatives, which includes substances such as methylone, methedrone and flephedrone. Over the last two years, mephedrone and mephedrone-containing products have been aggressively marketed by online suppliers as a legal alternative to ecstasy, amphetamines or cocaine.
(1) Europol–EMCDDA joint report on a new psychoactive substance: 4-methylmethcathinone (mephedrone)
(2) See Monitoring new drugs brochure
Drugnet Europe is the EMCDDA's newsletter launched in September 1996. The newsletter provides regular and succint information on the Centre's projects and activities to a broad readership.