Overview

Purevax RCPCh is a veterinary vaccine that used to vaccinate cats from the age of 8 weeks against the following diseases:

  • feline viral rhinotracheitis (a flu-like illness caused by a herpesvirus),
  • feline calicivirosis (a flu-like illness with inflammation of the mouth caused by a calicivirus),
  • feline chlamydiosis (a flu-like illness caused by the bacterium C. felis),
  • feline panleucopenia (a serious illness causing bloody diarrhoea caused by a parvovirus).

The vaccine helps to reduce the symptoms of the diseases. It can also prevent death due to panleucopenia.

Purevax RCPCh contains:

  • attenuated (weakened) feline rhinotracheitis herpesvirus (FHV F2 strain),
  • inactivated (killed) calicivirosis antigens (FCV 431 and G1 strains),
  • attenuated Chlamydophila felis (905 strain),
  • attenuated feline panleucopenia virus (PLI IV).

Purevax RCPCh is available as a lyophilisate (freeze-dried pellet) and solvent that are made up into a suspension for injection. The vaccine is given as two doses injected under the skin. The first injection should be given in kittens aged at least eight weeks, with a second injection three to four weeks later. If the kitten has high levels of antibodies received from the mother in the womb and in the milk, the first vaccination should be delayed until 12 weeks of age. The cat should be revaccinated for all components one year after the first vaccination course, then every year for chlamydiosis, and every three years for rhinotracheitis, calicivirosis and panleucopenia.

For more information about using Purevax RCPCh, see the package leaflet or contact your veterinarian or pharmacist.

Purevax RCPCh is a vaccine. Vaccines work by ‘teaching’ the immune system (the body’s natural defences) how to defend itself against a disease. Purevax RCPCh contains small amounts of weakened or killed viruses and bacteria that cause feline rhinotracheitis, calicivirosis, chlamydiosis and panleucopenia.

When a cat is given the vaccine, the immune system recognises the weakened or killed viruses and the weakened bacteria as ‘foreign’ and makes antibodies against them. In the future, the immune system will be able to produce antibodies more quickly when it is again exposed to the viruses or bacteria. The antibodies will help to protect against the diseases caused by these viruses or bacteria. When exposed to any of these viruses later in life, the cat will either not become infected or have a much less serious infection.

The effectiveness of Purevax RCPCh has been studied in several trials in laboratory conditions where cats were vaccinated and infected with herpesvirus, calicivirus, C. felis or parvovirus. In the field, the studies of Purevax RCPCh looked at the basic vaccination schedule (2 injections 3–4 weeks apart) and at the booster vaccination. They included young and adult cats of various breeds, but not young kittens. The main measure of effectiveness was the level of antibodies in the blood against the viruses and bacteria in the vaccine.

In laboratory conditions Purevax RCPCh was demonstrated to provide protection against the diseases listed above. In the field study of basic vaccination there was an increase in antibodies against feline rhinotracheitis herpesvirus, calicivirus infection, and feline panleucopenia viruses. It was not possible to detect a rise in antibodies against C. felis because of high levels of antibodies in the cats at the beginning of the study. In the study looking at booster vaccination, antibody levels against rhinotracheitis herpesvirus, calicivirus infection, feline panleucopenia and C. felis remained stable at a high level or increased slightly.

The most common side effects with Purevax RCPCh (which may affect up to 1 in 10 animals) are temporary apathy (loss of interest in surroundings) and anorexia (loss of appetite), as well as hyperthermia (elevated body temperature) lasting for one or two days. There may be a local reaction at the injection site, with slight pain on touching, itching or oedema (swelling), which disappears within one or two weeks.

Purevax RCPCh should not be used in pregnant cats and during lactation.

For the full list of side effects and restrictions of Purevax RCPCh, see the package leaflet.

In case of accidental self-injection medical advice should be sought immediately and the package leaflet or the label shown to the doctor. The vaccine should not be handled by people with a weak immune system. If self-injection does occur in these people, tell the doctor that self-injection with a living chlamydial vaccine has occurred.

The European Medicines Agency decided that Purevax RCPCh’s benefits are greater than its risks and it can be authorised for use in the EU.

Purevax RCPh received a marketing authorisation valid throughout the EU on 23 February 2005.

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Latest procedure affecting product information: WS2201/0034

17/02/2022

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Product details

Name of medicine
Purevax RCPCh
Active substance
  • attenuated feline rhinotracheitis herpesvirus (FHV F2 strain)
  • inactivated feline calicivirosis antigens (FCV 431 and G1 strains)
  • attenuated Chlamydophila felis (905 strain)
  • attenuated feline panleucopenia virus (PLI IV)
International non-proprietary name (INN) or common name
Vaccine against feline viral rhinotracheitis, feline calicivirosis, feline panleucopenia and feline Chlamydophila infections
Species
Cats
Anatomical therapeutic chemical veterinary (ATCvet) code
QI06AJ03

Pharmacotherapeutic group

Immunologicals for felidae

Therapeutic indication

Active immunisation of cats aged eight weeks and older:

• against feline viral rhinotracheitis to reduce clinical signs;

• against calicivirus infection to reduce clinical signs;

• against Chlamydophila felis infection to reduce clinical signs;

• against feline panleucopenia to prevent mortality and clinical signs.

Onsets of immunity have been demonstrated one week after primary vaccination course for rhinotracheitis, calicivirus, Chlamydophila felis and panleucopenia components.

The duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and one

year after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Authorisation details

EMA product number
EMEA/V/C/000088
Marketing authorisation holder
Boehringer Ingelheim Vetmedica GmbH

55216 Ingelheim am Rhein
Germany

Marketing authorisation issued
23/02/2005
Revision
17

Assessment history

News on Purevax RCPCh

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