Animal Medicines - what to do if you suspect an adverse reaction
What do you do if you suspect that you, or your animal, has suffered an
unexpected bad reaction to an animal
medicine?
Thankfully, harmful, unexpected
side-effects to animal medicines are very rare. Before any animal medicine is allowed
onto the UK market it has, by law, to satisfy very strict criteria on its quality, its
effectiveness and its safety.
However, once a medicine is in use, it is vital to know if any animals
or people exposed to it do suffer problems.
The Veterinary Medicines Directorate,
which administers the licensing system, runs a scheme to monitor reports of these
reactions in animals and people, called the Suspected Adverse Reaction Surveillance
Scheme. And a new leaflet produced by the VMD, which has been welcomed by the National
Office of Animal Health, outlines the scheme and includes some advice on what to do if you
think you may have a problem.
Sometimes an animal may show some small reaction to a medicine which is
normal - just like when babies receive their first vaccinations
they often get a slight temperature. But, if your animal is unwell or if you are at all
worried, contact your vet. "This is just common-sense whether or not your animal has
received medication," said NOAH director Roger Cook. "And it is more than likely
that an illness is totally unrelated to a medicine. If you suspect that the problem may be
due to a medicine and it is one not prescribed by your vet, bring the packet with you and
details of where you bought it. The vet will then have all the facts and can make an
accurate diagnosis of the true cause of the problem."
Similarly, if you think you may be affected, contact your doctor for
advice or treatment. Likewise, it would be helpful to bring the medicine packet with you.
And finally, if an adverse
reaction to an animal medicine is diagnosed, it should be reported to the scheme. Your
vet or doctor will normally do this: they are actively encouraged to do so by both the VMD
and NOAH, but the VMD welcomes anyone reporting such adverse reactions they have
experienced or observed. The form for doing this has just been updated, so it is easier to
include all the relevant information.
The purpose of the scheme is to monitor trends in reactions and once
the forms are received by the VMD they are prioritised in terms of severity to see whether
the problem is likely to be linked to the medicine, whether there have been any other
reports about the same product or others like it, whether any further information is
required and whether any follow-up is required.
Welcoming the new leaflet and the improved VMD reporting form, NOAH
director Roger Cook said: 'Only by professionals and owners taking the trouble to report
any problems can the VMD and companies get an idea of any action that needs to be taken.
We encourage reports, but are pleased that there are so few. This shows that the
authorisation system for animal medicines is doing its job and protecting animals and the
public from potential danger.'
Forms are available from The Suspected Adverse Reaction Surveillance
Scheme, Freepost KT4503, Veterinary Medicines Directorate, Woodham Lane, Addlestone,
Surrey KT15 3BR, telephone 01932 338427.
3 June 1999
Notes for Editors
For further information contact Roger Cook or Alison
Glennon at NOAH, tel. +44 (0)20 8367 3131, or visit the NOAH
website.
The National Office of Animal Health was formed on 1
January 1986 to represent the UK companies which research, develop, manufacture and market
licensed animal health products. The association has 34 corporate members and 10 associate members.
In 1998 NOAH's members accounted for around 95% of the £384 million UK animal health
market, with additional valuable exports
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