These are medicines licensed for use in the horse that are authorised for use in the food chain and are listed in table 1 of EC 37/2010.
The ability to use these medicines is usually contained in the summary of product characteristics (SPC or 'data sheet') included as a package insert or via the VMD Product Information database.
There are substances (e.g. some anaesthetic agents like ketamine and isoflurane, some antimicrobials like ceftiofur, some non-steroidal anti-inflammatories (NSAIDs) like carprofen and some substances used in breeding management like cloprostenol) that are 'allowed' in the European Regulation but which have UK marketing authorisations excluding their use in food-producing horses and requiring the horse to be declared not for human consumption. When there is a difference between the European Regulation and the UK Marketing Authorisation such substances can be used in food-producing horses provided that:
- the prescribing cascade is followed.
- a minimum meat withholding time of 28 days is set and a record is made in the passport (although this is at the discretion of the veterinary surgeon).
There is a requirement for owners to maintain a medicines record if horses are not signed out of the food chain in their passport. This can be recorded in the passport or in a separate document.
It is the responsibility of veterinary surgeons to inform owners of the likely withdrawal period although there are medicine for which no maximum residue limits (MRLs) are required (e.g. detomidine, butorphanol, ketoprofen, lidocaine, dembrexine, deslorelin).