Purevax RCP

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

attenuated feline panleucopenia virus (PLI IV)

Available from:

Boehringer Ingelheim Vetmedica GmbH

ATC code:

QI06AH09

INN (International Name):

vaccine against feline viral rhinotracheitis, feline calicivirosis and feline panleucopenia

Therapeutic group:

mačke

Therapeutic area:

Imunomodulatori za mačke,

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 feline panleucopenia to prevent mortality and clinical signs. Onset of immunity is one week after primary vaccination course The duration of immunity is one year after the primary vaccination course and three years after the last re-vaccination.

Product summary:

Revision: 17

Authorization status:

odobren

Authorization date:

2005-02-23

Patient Information leaflet

                                15
B. UPUTA O VMP
16
UPUTA O VMP
PUREVAX RCP LIOFILIZAT I OTAPALO ZA SUSPENZIJU ZA INJEKCIJU
1.
NAZIV I ADRESA NOSITELJA ODOBRENJA ZA STAVLJANJE VMP U PROMET I
NOSITELJA ODOBRENJA ZA PROIZVODNJU ODGOVORNOG ZA PUŠTANJE
PROIZVODNE SERIJE, AKO JE RAZLIČITO
Nositelj odobrenja za stavljanje u promet:
Boehringer Ingelheim Vetmedica GmbH
55216 Ingelheim/Rhein
NJEMAČKA
Proizvođač
odgovoran za puštanje serije u promet:
Boehringer Ingelheim Animal Health France SCS
Laboratoire Porte des Alpes
Rue de l'Aviation
69800 Saint-Priest
FRANCUSKA
2.
NAZIV VETERINARSKO-MEDICINSKOG PROIZVODA
Purevax RCP liofilizat i otapalo za suspenziju za injekciju.
3.
NAVOĐENJE DJELATNE(IH) TVARI I DRUGIH SASTOJAKA
Po dozi od 1 ml ili 0,5 ml:
LIOFILIZAT:
DJELATNA TVAR:
Atenuirani herpes virus rinotraheitisa mačaka (soj FHV F2)
..........................................
≥
10
4,9
CCID
50
1
Inaktivirani antigeni kalicivirusa mačaka (soj FCV 431 i FCV G1)
............................... .
≥
2,0 ELISA U.
Atenuirani virus panleukopenije mačaka (PLI IV)
.........................................................
≥
10
3,5
CCID
50
1
POMOĆNA TVAR:
Gentamicin, najviše
.......................................................................................................................
16,5 µg
OTAPALO:
Voda za injekcije
..........................................................................................................
q.s. 1 ml ili 0,5 ml
1
količina virusa koja zarazi 50 posto stanica kulture u koju je dodan
virus
Liofilizat: homogeni bež pelet.
Otapalo: bistra bezbojna tekućina.
4.
INDIKACIJA(E)
Aktivna imunizacija mačaka starijih od 8 tjedana:
-
protiv virusnog rinotraheitisa mačaka za smanjenje kliničkih
znakova,
-
protiv infekcije kalicivirusom za smanjenje kliničkih znakova,
-
protiv panleukopenije mačaka za sprječavanje smrtnosti i kliničkih
znakova.
Pokazalo se da imunitet nastupa 1 tjedan nakon prve vakcinacije.
17
Trajanje imunosti: 1 godina nakon prve vakcinacije i 3 godine nakon
zadnje revakcinacije.
5.
KONTRAIND
                                
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Summary of Product characteristics

                                1
DODATAK I
SAŽETAK OPISA SVOJSTAVA
2
1.
NAZIV VETERINARSKO-MEDICINSKOG PROIZVODA
Purevax RCP liofilizat i otapalo za suspenziju za injekcije
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Po dozi od 1 ml ili 0,5 ml:
Liofilizat:
DJELATNE TVARI:
Atenuirani herpes virus rinotraheitisa mačaka (soj FHV F2)
........................................
≥
10
4,9
CCID
50
1
Inaktivirani antigeni kalicivirusa mačaka,(soj FCV 431 i G1)
........................................
≥
2,0 ELISA U.
Atenuirani virus panleukopenije mačaka (PLI IV)
........................................................
≥
10
3,5
CCID
50
1
POMOĆNA TVAR:
Gentamicin, najviše
.......................................................................................................................
16,5 µg
Otapalo:
Voda za injekcije
..........................................................................................................
q.s. 1 ml ili 0,5 ml
1
količina virusa koja zarazi 50 posto stanica kulture u koju je dodan
virus
Potpuni popis pomoćnih tvari vidi u odjeljku 6.1.
3.
FARMACEUTSKI OBLIK
Liofilizat i otapalo za suspenziju za injekciju.
Liofilizat: homogeni bež pelet.
Otapalo: bistra bezbojna tekućina.
4.
KLINIČKE POJEDINOSTI
4.1
CILJNE VRSTE ŽIVOTINJA
Mačke.
4.2
INDIKACIJE ZA PRIMJENU, NAVESTI CILJNE VRSTE ŽIVOTINJA
Aktivna imunizacija mačaka starijih od 8 tjedana:
-
protiv virusnog rinotraheitisa mačaka za smanjenje kliničkih
znakova,
-
protiv infekcije kalicivirusom za smanjenje kliničkih znakova,
-
protiv panleukopenije mačaka za sprječavanje smrtnosti i kliničkih
znakova.
Pokazalo se da imunost nastupa 1 tjedan nakon prve vakcinacije.
Trajanje imunosti: 1 godina nakon prve vakcinacije i 3 godine nakon
zadnje revakcinacije.
4.3
KONTRAINDIKACIJE
Nema.
4.4
POSEBNA UPOZORENJA ZA SVAKU OD CILJNIH VRSTA ŽIVOTINJA
Cijepiti samo zdrave životinje.
3
4.5
POSEBNE MJERE OPREZA PRILIKOM PRIMJENE
Posebne mjere opreza prilikom primjene na životinjama
Nema.
Posebne mjere opreza koje mora poduzeti osoba koja primjenjuje
veterinarsko-med
                                
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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 08-03-2021
Patient Information leaflet Patient Information leaflet Spanish 06-04-2022
Public Assessment Report Public Assessment Report Spanish 08-03-2021
Patient Information leaflet Patient Information leaflet Czech 06-04-2022
Public Assessment Report Public Assessment Report Czech 08-03-2021
Patient Information leaflet Patient Information leaflet Danish 06-04-2022
Public Assessment Report Public Assessment Report Danish 08-03-2021
Patient Information leaflet Patient Information leaflet German 06-04-2022
Public Assessment Report Public Assessment Report German 08-03-2021
Patient Information leaflet Patient Information leaflet Estonian 06-04-2022
Public Assessment Report Public Assessment Report Estonian 08-03-2021
Patient Information leaflet Patient Information leaflet Greek 06-04-2022
Public Assessment Report Public Assessment Report Greek 08-03-2021
Patient Information leaflet Patient Information leaflet English 06-04-2022
Public Assessment Report Public Assessment Report English 08-03-2021
Patient Information leaflet Patient Information leaflet French 06-04-2022
Public Assessment Report Public Assessment Report French 08-03-2021
Patient Information leaflet Patient Information leaflet Italian 06-04-2022
Public Assessment Report Public Assessment Report Italian 08-03-2021
Patient Information leaflet Patient Information leaflet Latvian 06-04-2022
Public Assessment Report Public Assessment Report Latvian 08-03-2021
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 08-03-2021
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 08-03-2021
Patient Information leaflet Patient Information leaflet Maltese 06-04-2022
Public Assessment Report Public Assessment Report Maltese 08-03-2021
Patient Information leaflet Patient Information leaflet Dutch 06-04-2022
Public Assessment Report Public Assessment Report Dutch 08-03-2021
Patient Information leaflet Patient Information leaflet Polish 06-04-2022
Public Assessment Report Public Assessment Report Polish 08-03-2021
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 08-03-2021
Patient Information leaflet Patient Information leaflet Romanian 06-04-2022
Public Assessment Report Public Assessment Report Romanian 08-03-2021
Patient Information leaflet Patient Information leaflet Slovak 06-04-2022
Public Assessment Report Public Assessment Report Slovak 08-03-2021
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 08-03-2021
Patient Information leaflet Patient Information leaflet Finnish 06-04-2022
Public Assessment Report Public Assessment Report Finnish 08-03-2021
Patient Information leaflet Patient Information leaflet Swedish 06-04-2022
Public Assessment Report Public Assessment Report Swedish 08-03-2021
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

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