Flukicides for which no maximum residue limit has been established in milk and which are intended for use in ruminants producing milk for human consumption

Table of contents

Current status
European Commission final decision

Overview

Flukicidal substances are antihelminthics that are active against parasites belonging to the class trematodes.

On 14 February 2011, the European Commission initiated a referral procedure under Article 35 of Directive 2001/82/EC, as amended, for all veterinary medicinal products containing active substances belonging to the class of flukicides for which no maximum residue limit has been established in milk intended for use in all ruminants producing milk for human consumption. The flukicidal substances for which a maximum residue limit has not been established in milk and that are included as active substances in authorised veterinary medicinal products in the Member States (European Union and European Economic Area) are clorsulon, closantel, nitroxinil, rafoxanide and triclabendazole. The Committee for Medicinal Products for Veterinary Use (CVMP) was therefore requested to give its opinion as to whether measures are necessary to ensure that the use, during the non-lactating period, of veterinary medicinal products containing clorsulon, closantel, nitroxinil, rafoxanide and triclabendazole, would not lead to residues in milk that, combined with residues of these flukicidal substances from other foodstuffs, would result in consumer exposure exceeding the acceptable daily intake.

The referral started on 9 March 2011. The Committee appointed Mr G. J. Schefferlie as rapporteur and Dr B. Urbain as co-rapporteur. Supplementary information was provided by some of the applicants / marketing-authorisation holders by 26 August 2011. Written explanations were provided by a group of marketing-authorisation holders on 11 January 2012. Oral explanations were given by a group of marketing-authorisation holders on 8 February 2012.

Based on the evaluation of the available data, the CVMP adopted, on 8 March 2012, an opinion recommending variations of the marketing authorisations for the veterinary medicinal products containing clorsulon, closantel, nitroxinil, rafoxanide or triclabendazole as a single active substance and for the veterinary medicinal products administered as pour-on to cattle containing triclabendazole and moxidectin.

On 23 March 2012, Merial notified the Agency of its intention to request a re-examination of the CVMP opinion of 8 March 2012.

During its meeting of 11-13 April 2012, the CVMP appointed Dr C. Muñoz as the rapporteur and Dr E. Persson as the co-rapporteur for the re-examination procedure.

The detailed grounds for the re-examination request were submitted by Merial on 2 May 2012. The re-examination procedure started on 3 May 2012. The issues considered during the re-examination related to the recommended amendments of section 4.11 Withdrawal period(s) of the summaries of product characteristics for the veterinary medicinal products containing nitroxinil that are administered to cattle. Oral explanations were given by Merial on 16 May 2012.

On 14 June 2012, the CVMP adopted a final opinion confirming the recommendation, included in its opinion of 8 March 2012, that variations are necessary in the marketing authorisations for the veterinary medicinal products containing clorsulon, closantel, nitroxinil, rafoxanide or triclabendazole as a single active substance and for the veterinary medicinal products administered as pour-on to cattle containing triclabendazole and moxidectin in order to amend the summaries of product characteristics and package leaflets in line with recommended by the CVMP changes in the product information.

The list of product names concerned is given in annex I. The scientific conclusions are provided in annex II together with the amendments in the summaries of product characteristics and package leaflets in annex III.

The final opinion was converted into a decision by the European Commission on 19 November 2012.

Key facts

Approved name
Flukicides for which no maximum residue limit has been established in milk and which are intended for use in ruminants producing milk for human consumption
International non-proprietary name (INN) or common name
  • clorsulon
  • closantel
  • nitroxinil
  • rafoxanide
  • triclabendazole
Class
-
Current status
European Commission final decision
Reference number
EMEA/V/A/069
Type
Article 35

Community interest referral: initiated in cases involving the interests of the Community or concerns relating to the protection of human or animal health or the environment.
Opinion date
14/06/2012
EC decision date
19/11/2012

All documents

Description of documents published

Please note that some of the listed documents apply only to certain procedures.

  • Overview - lay-language summary of the stage of the procedure
  • Notification – a letter from a Member State, the European Commission or the marketing authorisation holder requesting the initiation of the procedure
  • List of questions – questions agreed by the Committee requesting further information from the marketing authorisation holder(s) / applicant(s) to evaluate the issues identified
  • Timetable for the procedure – agreed timeframe to respond to the list of questions, to assess the issues and to adopt a conclusion
  • List of medicines concerned by the procedure – medicine(s) / active substance(s) concerned, and marketing authorisation holder(s) / applicant(s)
  • List of questions to be addressed by the stakeholders – call for data to be submitted by stakeholders (e.g. veterinary healthcare professionals, farmers, academia) (if applicable)
  • Stakeholder submission form – form to be used by stakeholders to submit data (if applicable)
  • Scientific conclusions – scientific conclusions of CVMP
  • Divergent positions – divergent positions of the CVMP members (if applicable)
  • Changes to the summary of product characteristics, labelling and package leaflet (amended sections or fully revised version) (if applicable)
  • Condition(s) to the marketing authorisation(s) – condition(s) for the safe and effective use of the medicine(s) (if applicable)
  • Condition for lifting the suspension – condition to be fulfilled for the suspension of the marketing authorisation(s) to be lifted (if applicable)

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