Purevax RCPCh

Country: European Union

Language: Danish

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:

Katte

Therapeutic area:

Immunologicals for 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. Immunitetstrin har vist sig en uge efter primærvaccinationskursus for rhinotracheitis, calicivirus, Chlamydophila felis og panleucopenia komponenter. 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:

autoriseret

Authorization date:

2005-02-23

Patient Information leaflet

                                15
B.
INDLÆGSSEDDEL
16
INDLÆGSSEDDEL:
PUREVAX RCPCH LYOFILISAT OG SOLVENS TIL INJEKTIONSVÆSKE, SUSPENSION.
1.
NAVN OG ADRESSE PÅ INDEHAVEREN AF MARKEDSFØRINGSTILLADELSEN
SAMT PÅ DEN INDEHAVER AF VIRKSOMHEDSGODKENDELSE, SOM ER
ANSVARLIG FOR BATCHFRIGIVELSE, HVIS FORSKELLIG HERFRA
Indehaver af markedsføringstilladelsen:
Boehringer Ingelheim Vetmedica GmbH
55216 Ingelheim/Rhein
Tyskland
Fremstiller ansvarlig for batchfrigivelse:
Boehringer Ingelheim Animal Health France SCS
Laboratoire Porte des Alpes
Rue de l’Aviation
69800 Saint-Priest
Frankrig
2.
VETERINÆRLÆGEMIDLETS NAVN
Purevax RCPCh lyofilisat og solvens til injektionsvæske, suspension.
3.
ANGIVELSE AF DE(T) AKTIVE STOF(FER) OG ANDRE INDHOLDSSTOFFER
1 dosis (1 ml eller 0,5 ml) indeholder:
Lyofilisat:
AKTIVE STOFFER:
Svækket felin rhinotracheitis herpesvirus (FHV F2 stamme)
..........................................
≥
10
4,9
CCID
50
1
Inaktiverede feline calicivirusantigener (FCV 431 og G1 stammer)
..............................
≥
2,0 ELISA U.
Svækket
_Chlamydophila felis_
(905 stamme)
.......................................................................
≥
10
3,0
EID
50
2
Svækket felin panleukopenivirus (PLI IV)
.......................................................................
≥
10
3,5
CCID
50
1
HJÆLPESTOFFER:
Gentamycin max
..............................................................................................................................
28
µ
g
Solvens:
Vand til injektionsvæsker
.........................................................................................
q.s 1 ml eller 0,5 ml.
1
cellekultur infektiøs dosis 50%.
2
æg infektiøs dosis 50%.
Lyofilisat: homogen, beige pellet.
Solvens: klar, farveløs væske.
4.
INDIKATIONER
Aktiv immunisering af katte, der er 8 uger eller ældre:
−
mod felin viral rhinotracheitis for at reducere kliniske tegn,
−
mod calicivirus infektion for at reducere kliniske tegn,
−
mod
_Chlamydophila felis_
infektion for at reducere kliniske tegn,
−
mod felin panleukopeni til
                                
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Summary of Product characteristics

                                1
BILAG I
PRODUKTRESUME
2
1.
VETERINÆRLÆGEMIDLETS NAVN
Purevax RCPCh lyofilisat og solvens til injektionsvæske, suspension.
2.
KVALITATIV OG KVANTITATIV SAMMENSÆTNING
1 dosis (1 ml eller 0,5 ml) indeholder:
Lyofilisat:
AKTIVE STOFFER:
Svækket felin rhinotracheitis herpesvirus (FHV F2 stamme)
..........................................
≥
10
4,9
CCID
50
1
Inaktiverede feline calicivirusantigener (FCV 431 og G1 stammer)
................................
≥
2,0 ELISA U
Svækket
_Chlamydophila felis_
(905 stamme)
.......................................................................
≥
10
3,0
EID
50
2
Svækket felin panleukopenivirus (PLI IV)
.......................................................................
≥
10
3,5
CCID
50
1
HJÆLPESTOFFER:
Gentamycin max
.............................................................................................................................
28
µ
g
Solvens:
Vand til injektionsvæsker
..........................................................................................
q.s. 1 ml eller 0,5 ml
1
cellekultur infektiøs dosis 50%.
2
æg infektiøs dosis 50%.
Alle hjælpestoffer er anført under pkt. 6.1.
3.
LÆGEMIDDELFORM
Lyofilisat og solvens til injektionsvæske, suspension.
Lyofilisat: homogen, beige pellet.
Solvens: klar, farveløs væske.
4.
KLINISKE OPLYSNINGER
4.1
DYREARTER, SOM LÆGEMIDLET ER BEREGNET TIL
Kat.
4.2
TERAPEUTISKE INDIKATIONER MED ANGIVELSE AF DYREARTER, SOM LÆGEMIDLET
ER BEREGNET TIL
Aktiv immunisering af katte, der er 8 uger eller ældre:
−
mod felin viral rhinotracheitis for at reducere kliniske tegn,
−
mod calicivirus infektion for at reducere kliniske tegn,
−
mod
_Chlamydophila felis_
infektion for at reducere kliniske tegn,
−
mod felin panleukopeni til forebyggelse af dødsfald og kliniske tegn.
Det er vist, at immuniteten indtræder 1 uge efter basisvaccination
for
_ _
rhinotracheitis, calicivirus,
_Chlamydophila felis _
og panleukopeni.
Varighed af immunitet:
-
Rhinotracheitis, calicivirus og panleukopeni komponenterne: 1 å
                                
                                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 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
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Public Assessment Report Public Assessment Report French 09-03-2021
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Public Assessment Report Public Assessment Report Italian 09-03-2021
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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
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Public Assessment Report Public Assessment Report Maltese 09-03-2021
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Public Assessment Report Public Assessment Report Portuguese 09-03-2021
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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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