Purevax RCPCh

Country: European Union

Language: Dutch

Source: EMA (European Medicines Agency)

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Active ingredient:

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)

Available from:

Boehringer Ingelheim Vetmedica GmbH

ATC code:

QI06AJ03

INN (International Name):

vaccine against feline viral rhinotracheitis, feline calicivirosis, feline panleucopenia and feline Chlamydophila infections

Therapeutic group:

Cats

Therapeutic area:

Immunologicals voor felidae,

Therapeutic indications:

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 van immuniteit zijn aangetoond een week na de primaire vaccinatiekuur voor rhinotracheitis, calicivirus, Chlamydophila felis en panleucopenie componenten. The duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and oneyear after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Product summary:

Revision: 17

Authorization status:

Erkende

Authorization date:

2005-02-23

Patient Information leaflet

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Purevax RCPCh lyophilisate and solvent for suspension for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Per dose of 1 ml or 0.5 ml:
Lyophilisate:
ACTIVE SUBSTANCES:
Attenuated feline rhinotracheitis herpesvirus (FHV F2 strain)
......................................
≥
10
4.9
CCID
50
1
Inactivated feline calicivirus (FCV 431 and G1 strains) antigens
...................................
≥
2.0 ELISA U.
Attenuated
_Chlamydophila felis_
(905 strain)
.....................................................................
≥
10
3.0
EID
50
2
Attenuated feline panleucopenia virus (PLI IV)
............................................................
≥
10
3.5
CCID
50
1
EXCIPIENT:
Gentamicin, at most
..........................................................................................................................
28 µg
Solvent:
Water for injections
.....................................................................................................
q.s. 1 ml or 0.5 ml.
1
cell culture infective dose 50%
2
egg infective dose 50%
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Lyophilisate and solvent for suspension for injection.
Lyophilisate: homogeneous beige pellet.
Solvent: clear colourless liquid.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Cats.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Active immunisation of cats aged 8 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 1 week after primary
vaccination course for
rhinotracheitis, calicivirus,
_Chlamydophila felis_
and panleucopenia components.
Duration of immunity:
-
Rhinotracheitis, calicivirosis and panleucopenia components: 1 year
after primary vaccination
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Purevax RCPCh lyophilisate and solvent for suspension for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Per dose of 1 ml or 0.5 ml:
Lyophilisate:
ACTIVE SUBSTANCES:
Attenuated feline rhinotracheitis herpesvirus (FHV F2 strain)
......................................
≥
10
4.9
CCID
50
1
Inactivated feline calicivirus (FCV 431 and G1 strains) antigens
...................................
≥
2.0 ELISA U.
Attenuated
_Chlamydophila felis_
(905 strain)
.....................................................................
≥
10
3.0
EID
50
2
Attenuated feline panleucopenia virus (PLI IV)
............................................................
≥
10
3.5
CCID
50
1
EXCIPIENT:
Gentamicin, at most
..........................................................................................................................
28 µg
Solvent:
Water for injections
.....................................................................................................
q.s. 1 ml or 0.5 ml.
1
cell culture infective dose 50%
2
egg infective dose 50%
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Lyophilisate and solvent for suspension for injection.
Lyophilisate: homogeneous beige pellet.
Solvent: clear colourless liquid.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Cats.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Active immunisation of cats aged 8 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 1 week after primary
vaccination course for
rhinotracheitis, calicivirus,
_Chlamydophila felis_
and panleucopenia components.
Duration of immunity:
-
Rhinotracheitis, calicivirosis and panleucopenia components: 1 year
after primary vaccination
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 06-04-2022
Public Assessment Report Public Assessment Report Bulgarian 09-03-2021
Patient Information leaflet Patient Information leaflet Spanish 06-04-2022
Public Assessment Report Public Assessment Report Spanish 09-03-2021
Patient Information leaflet Patient Information leaflet Czech 06-04-2022
Public Assessment Report Public Assessment Report Czech 09-03-2021
Patient Information leaflet Patient Information leaflet Danish 06-04-2022
Public Assessment Report Public Assessment Report Danish 09-03-2021
Patient Information leaflet Patient Information leaflet German 06-04-2022
Public Assessment Report Public Assessment Report German 09-03-2021
Patient Information leaflet Patient Information leaflet Estonian 06-04-2022
Public Assessment Report Public Assessment Report Estonian 09-03-2021
Patient Information leaflet Patient Information leaflet Greek 06-04-2022
Public Assessment Report Public Assessment Report Greek 09-03-2021
Patient Information leaflet Patient Information leaflet English 06-04-2022
Public Assessment Report Public Assessment Report English 09-03-2021
Patient Information leaflet Patient Information leaflet French 06-04-2022
Public Assessment Report Public Assessment Report French 09-03-2021
Patient Information leaflet Patient Information leaflet Italian 06-04-2022
Public Assessment Report Public Assessment Report Italian 09-03-2021
Patient Information leaflet Patient Information leaflet Latvian 06-04-2022
Public Assessment Report Public Assessment Report Latvian 09-03-2021
Patient Information leaflet Patient Information leaflet Lithuanian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 06-04-2022
Public Assessment Report Public Assessment Report Lithuanian 09-03-2021
Patient Information leaflet Patient Information leaflet Hungarian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 06-04-2022
Public Assessment Report Public Assessment Report Hungarian 09-03-2021
Patient Information leaflet Patient Information leaflet Maltese 06-04-2022
Public Assessment Report Public Assessment Report Maltese 09-03-2021
Patient Information leaflet Patient Information leaflet Polish 06-04-2022
Public Assessment Report Public Assessment Report Polish 09-03-2021
Patient Information leaflet Patient Information leaflet Portuguese 06-04-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 06-04-2022
Public Assessment Report Public Assessment Report Portuguese 09-03-2021
Patient Information leaflet Patient Information leaflet Romanian 06-04-2022
Public Assessment Report Public Assessment Report Romanian 09-03-2021
Patient Information leaflet Patient Information leaflet Slovak 06-04-2022
Public Assessment Report Public Assessment Report Slovak 09-03-2021
Patient Information leaflet Patient Information leaflet Slovenian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 06-04-2022
Public Assessment Report Public Assessment Report Slovenian 09-03-2021
Patient Information leaflet Patient Information leaflet Finnish 06-04-2022
Public Assessment Report Public Assessment Report Finnish 09-03-2021
Patient Information leaflet Patient Information leaflet Swedish 06-04-2022
Public Assessment Report Public Assessment Report Swedish 09-03-2021
Patient Information leaflet Patient Information leaflet Norwegian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 06-04-2022
Patient Information leaflet Patient Information leaflet Icelandic 06-04-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 06-04-2022
Patient Information leaflet Patient Information leaflet Croatian 06-04-2022
Public Assessment Report Public Assessment Report Croatian 09-03-2021

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