VMD Medicines Update - August 2020 | British Equine Veterinary Association
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VMD Medicines Update - August 2020

Medicines News
02 Oct 2020 BEVA

New MAs and changes made and published to end of August 2020

The points below highlight changes in marketing authorisations (MAs) that may have a significant impact on veterinary surgeons’ prescribing decisions.

New marketing authorisations

New marketing authorisations relevant to veterinary surgeons in the UK that were issued or published in August are listed in Table 1.

Table 1 also indicates where a public assessment report should become available for a product. Where available, links to these reports are accessible by clicking on the relevant product on the VMD’s Product Information Database https://www.gov.uk/check-animal-medicine-licensed

The European Medicines Agency (EMA) publishes European Public Assessment Reports (EPARs) for every veterinary medicine which is authorised through a centralised procedure. Links to these reports are accessible on http://www.ema.europa.eu

 

TABLE 1

Marketing Authorisations issued/published in August 2020

Product name

Active substance

Authorisation Holder

Public Assessment Report to be made available from VMD?

 

Bimeprazol 370 mg/g oral paste for horses

Omeprazole

Oy Medfiles Ltd

Yes

Emdofluxin 50 mg/ml, solution for injection for cattle, pigs and horses

Flunixin

Emdoka bvba

No – RMS France

Peptaleve 370 mg/g oral paste for horses

Omeprazole

Norbrook Laboratories (Ireland) Limited

No RMS Ireland


Please note that there may be a delay between the issuing of a marketing authorisation to a company and the product being placed on the market.

In prescribing these veterinary medicines, veterinary surgeons should be aware that changes to the Summary of Product Characteristics (SPC), labels and leaflets may, in certain cases, change how the medicines should be used. The timing of when such changes have to be taken into account will depend on the circumstances, but as a general rule unless a prescriber has been advised otherwise by the manufacturer or the VMD the labelling instructions on the pack from which the product is dispensed should be followed.

VMD contact for this article: Vivienne Saville; v.saville@vmd.gov.uk