A new report from the working group set up as part of the Veterinary Products Committee in response to public and scientific concern about the possible health risks attached to annual vaccinations in dogs and cats issued the following final recommendations:
Data showed that the incidence of adverse reactions to dog and cat vaccines per 10 000 doses of product was "relatively low". However under-reporting was said to be a feature of such surveillance. The committee admitted that due to a number of constraints, the analysis was not fully comprehensive and the "interaction of possible risk factors" was not determined. Evidence should that cats occasionally develop sarcomas at sites of injection and the there is evidence that although other products may be involved, these may be associated with vaccines containing aluminium-based adjuvant. It was also agreed in view of the occasional occurrence of adverse reactions that product literature should indicate that the yearly booster vaccinations was based on a minimum duration of immunity rather than a maximum.
Although for some diseases there is evidence of a longer duration of immunity following vaccination that the one year which is typically recommended on the product literature, there is currently insufficient information to propose re-vaccination intervals other that those proposed by the manufacturer and approved by the regulatory process.
The full report is available from the DEFRA Publications, Admail 6000, London. SW1A 2XX. It is also on the VPC's website as www.vpc.gov.uk