Report on the risk assessment of ketamine in the framework of the joint action on new synthetic drugs

Introduction

Since the mid-1990s, ketamine – widely used in human and veterinary medicine for 30 years – has been surfacing as a recreational drug. Concern over ketamine centres on its unpredictability in producing ‘near-death’ experiences. The risk-assessment exercise was carried out in 2000 in the framework of the Joint action on new synthetic drugs. In March 2001, the EU Justice and Home Affairs Council adopted formal conclusions that Member States should monitor this drug closely. This publication records the findings and conclusions of the exercise. Among others, it draws together the various elements used to assess the substance including: the final risk-assessment report; contributions from Europol and the European Agency for the Evaluation of Medicinal Products; a review of pharmacotoxicological data; epidemiological evidence on the associated public-health risks and sociological and criminological evidence.

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Table of contents

  • Report on the risk assessment of ketamine in the framework of the joint action on new synthetic drugs
  • Europol-EMCDDA progress report on ketamine in accordance with Article 3 on the joint action of 16 June 1997 concerning the information exchange, risk assessment and the control of new synthetic drugs
  • Use of ketamine in human medicine in the EU Member States
  • Use of ketamine in veterinary medicine in the EU Member States
  • Review of the pharmacotoxicological data on ketamine (2-(2-chlorophenyl)-2-(methyloamino)-cyclohexanone)
  • Sociological and criminological (Europol) evidence
  • Public health risks - epidemiological evidence
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