Purevax RCP

Country: European Union

Language: Italian

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:

Gatti

Therapeutic area:

Prodotti immunologici per 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 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:

autorizzato

Authorization date:

2005-02-23

Patient Information leaflet

                                14
B. FOGLIETTO ILLUSTRATIVO
15
FOGLIETTO ILLUSTRATIVO:
PUREVAX RCP LIOFILIZZATO E SOLVENTE PER SOSPENSIONE INIETTABILE
1.
NOME E INDIRIZZO DEL TITOLARE DELL’AUTORIZZAZIONE
ALL’IMMISSIONE IN COMMERCIO E DEL TITOLARE DELL’AUTORIZZAZIONE
ALLA PRODUZIONE RESPONSABILE DEL RILASCIO DEI LOTTI DI
FABBRICAZIONE, SE DIVERSI
Titolare dell’autorizzazione all’immissione in commercio:
Boehringer Ingelheim Vetmedica GmbH
55216 Ingelheim/Rhein
GERMANIA
Produttore responsabile del rilascio dei lotti di fabbricazione:
Boehringer Ingelheim Animal Health France SCS
Laboratoire Porte des Alpes
Rue de l’Aviation
69800 Saint-Priest
FRANCIA
2.
DENOMINAZIONE DEL MEDICINALE VETERINARIO
Purevax RCP liofilizzato e solvente per sospensione iniettabile.
3.
INDICAZIONE DEL(I) PRINCIPIO(I) ATTIVO(I) E DEGLI ALTRI INGREDIENTI
In una dose da 1 ml o da 0,5 ml:
LIOFILIZZATO:
PRINCIPI ATTIVI:
Herpesvirus attenuato della rinotracheite felina (ceppo FHV F2)
...................................
≥
10
4,9
DICC
50
1
Antigeni del calicivirus felino inattivato (ceppi FCV 431 e G1)
...................................
≥
2,0 U. ELISA
Virus attenuato della panleucopenia felina (PLI IV)
.......................................................
≥
10
3,5
DICC
50
1
ECCIPIENTE:
Gentamicina,
max.........................................................................................................................
16,5 µg
SOLVENTE:
Acqua per preparazioni iniettabili
..........................................................................
q.b. a 1 ml o a 0,5 ml.
1
dose infettante il 50% delle colture cellulari.
Liofilizzato: pellet beige omogeneo.
Solvente: liquido limpido incolore.
4.
INDICAZIONE(I)
Immunizzazione attiva dei gatti di 8 settimane, o più, di età:
-
nei confronti della rinotracheite virale felina, per la riduzione dei
sintomi clinici,
-
nei confronti della infezione da calicivirus felino, per la riduzione
dei sintomi clinici,
-
nei confronti della panleucopenia felina, per la prevenzione della
mortalità e dei sintomi clinici.
Inizi
                                
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Summary of Product characteristics

                                1
ALLEGATO I
RIASSUNTO DELLE CARATTERISTICHE DEL PRODOTTO
2
1.
DENOMINAZIONE DEL MEDICINALE VETERINARIO
Purevax RCP liofilizzato e solvente per sospensione iniettabile
2.
COMPOSIZIONE QUALITATIVA E QUANTITATIVA
In una dose da 1 ml o da 0,5 ml:
Liofilizzato:
PRINCIPI ATTIVI:
Herpesvirus attenuato della rinotracheite felina (ceppo FHV F2)
...................................
≥
10
4,9
DICC
50
1
Antigeni del calicivirus felino inattivato (ceppi FCV 431 e G1)
...................................
≥
2,0 U. ELISA
Virus attenuato della panleucopenia felina (PLI IV)
.......................................................
≥
10
3,5
DICC
50
1
ECCIPIENTE:
Gentamicina, max
................................................................................................................
16,5 µg
Solvente:
Acqua per preparazioni iniettabili
...........................................................................
q.b. a 1 ml o a 0,5 ml
1
dose infettante il 50% delle colture cellulari.
Per l’elenco completo degli eccipienti, vedere paragrafo 6.1.
3.
FORMA FARMACEUTICA
Liofilizzato e solvente per sospensione iniettabile.
Liofilizzato: pellet beige omogeneo.
Solvente: liquido limpido incolore.
4.
INFORMAZIONI CLINICHE
4.1
SPECIE DI DESTINAZIONE
Gatti.
4.2
INDICAZIONI PER L’UTILIZZAZIONE SPECIFICANDO LE SPECIE DI
DESTINAZIONE
Immunizzazione attiva dei gatti di 8 settimane, o più, di età:
-
nei confronti della rinotracheite virale felina, per la riduzione dei
sintomi clinici,
-
nei confronti della infezione da calicivirus felino, per la riduzione
dei sintomi clinici,
-
nei confronti della panleucopenia felina, per la prevenzione della
mortalità e dei sintomi clinici.
Inizio dell’immunità: 1 settimana dopo la vaccinazione di base.
Durata dell’immunità: 1 anno dopo la vaccinazione di base e 3 anni
dopo l’ultimo richiamo vaccinale.
4.3
CONTROINDICAZIONI
Nessuna
4.4
AVVERTENZE SPECIALI PER CIASCUNA SPECIE DI DESTINAZIONE
Vaccinare solo animali sani.
3
4.5
PRECAUZIONI SPECIALI PER L’IMPIEGO
Precauzioni speciali per l
                                
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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
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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
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Public Assessment Report Public Assessment Report Estonian 08-03-2021
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Public Assessment Report Public Assessment Report Greek 08-03-2021
Patient Information leaflet Patient Information leaflet English 06-04-2022
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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
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Public Assessment Report Public Assessment Report Maltese 08-03-2021
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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
Patient Information leaflet Patient Information leaflet Croatian 06-04-2022
Public Assessment Report Public Assessment Report Croatian 08-03-2021

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