Purevax RCPCh

Country: European Union

Language: Romanian

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:

Pisici

Therapeutic area:

Produsele imunologice pentru 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. Incidența imunității a fost demonstrată la o săptămână după vaccinarea primară pentru rinotraheită, calicivirus, Chlamydophila felis și componentele panleucopeniei. 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:

Autorizat

Authorization date:

2005-02-23

Patient Information leaflet

                                15
B. PROSPECT
16
PROSPECT
PUREVAX RCPCH LIOFILIZAT ŞI SOLVENT PENTRU SUSPENSIE INJECTABILĂ
1.
NUMELE ŞI ADRESA DEŢINĂTORULUI AUTORIZAŢIEI DE COMERCIALIZARE
ŞI A DEŢINĂTORULUI AUTORIZAŢIEI DE FABRICAŢIE, RESPONSABIL
PENTRU ELIBERAREA SERIILOR DE PRODUS, DACĂ SUNT DIFERITE
Deţinătorul autorizaţiei de comercializare:
Boehringer Ingelheim Vetmedica GmbH
55216 Ingelheim/Rhein
GERMANIA
Producător responsabil pentru eliberarea seriei:
Boehringer Ingelheim Animal Health France SCS
Laboratoire Porte des Alpes
Rue de l'Aviation
69800 Saint Priest
FRANȚA
2.
DENUMIREA PRODUSULUI MEDICINAL VETERINAR
Purevax RCPCh
Liofilizat şi solvent pentru suspensie injectabilă.
3.
DECLARAREA (SUBSTANŢEI) SUBSTANŢELOR ACTIVE ŞI A ALTOR
INGREDIENTE (INGREDIENŢI)
Pentru o doză de 1 ml sau 0,5 ml:
LIOFILIZAT:
SUBSTANȚE ACTIVE:
Herpesvirus atenuat al rinotraheitei feline (tulpina FHV F2)
...........................................
≥
10
4,9
DICC
50
1
Antigene inactivate ale calicivirozei feline (tulpinile FCV 431 şi
G1) ............................
≥
2,0 ELISA U
_Chlamydophila felis_
atenuat (tulpina 905)
........................................................................
≥
10
3,0
DIE
50
2
Virus atenuat al panleucopeniei feline (PLI IV)
.............................................................
≥
10
3,5
DICC
50
1
EXCIPIENT:
Gentamicină, maximum
...................................................................................................................
28 µg
SOLVENT:
Apă pentru injecţii
.....................................................................................................
q.s. 1 ml sau0,5 ml
1
doză infectantă pe culturi celulare 50%
2
doză infectantă embrionară 50%
Liofilizat: peletă bej omogenă.
Solvent: lichid incolor limpede.
4.
INDICAŢIE (INDICAŢII)
Imunizarea activă a pisicilor în vârstă de 8 săptămâni şi mai
mari:
-
împotriva rinotraheitei virale feline pentru reducerea semnelor
clinice,
-
împotriva infecţiei cu calicivirus pentru reducerea semnelor
cli
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANEXA I
REZUMATUL CARACTERISTICILOR PRODUSULUI
2
1.
DENUMIREA PRODUSULUI MEDICINAL VETERINAR
Purevax RCPCh liofilizat şi solvent pentru suspensie injectabilă.
2.
COMPOZIŢIA CALITATIVĂ ŞI CANTITATIVĂ
Pentru o doză de 1 ml sau 0,5ml:
Liofilizat:
SUBSTANŢE ACTIVE:
Herpesvirus atenuat al rinotraheitei feline (tulpina FHV F2)
...........................................
≥
10
4,9
DICC
50
1
Antigene inactivate ale calicivirozei feline (tulpinile FCV 431 şi
G1) ............................
≥
2,0 ELISA U
_Chlamydophila felis _
atenuat (tulpina 905)
......................................................................
≥
10
3,0
DIE
50
2
Virus atenuat al panleucopeniei feline (PLI IV)
.............................................................
≥
10
3,5
DICC
50
1
EXCIPIENT:
Gentamicină, maximum
...................................................................................................................
28 µg
Solvent:
Apă pentru injecţii
.....................................................................................................
q.s 1 ml sau 0,5 ml
1
doză infectantă pe culturi celulare 50%
2
doză infectantă embrionară 50%
Pentru lista completă a excipienţilor, vezi secţiunea 6.1.
3.
FORMA FARMACEUTICĂ
Liofilizat şi solvent pentru suspensie injectabilă.
Liofilizat: peletă bej omogenă.
Solvent: lichid incolor limpede.
4.
PARTICULARITĂŢI CLINICE
4.1.
SPECII ŢINTĂ
Pisici.
4.2.
INDICAŢII PENTRU UTILIZARE, CU SPECIFICAREA SPECIILOR ȚINTĂ
Imunizarea activă a pisicilor în vârstă de 8 săptămâni şi mai
mari:
-
împotriva rinotraheitei virale feline pentru reducerea semnelor
clinice,
-
împotriva infecţiei cu calicivirus pentru reducerea semnelor
clinice,
-
împotriva infecţiilor cu
_ Chlamydophila felis_
pentru reducerea semnelor clinice,
-
împotriva panleucopeniei feline pentru prevenirea mortalităţii şi
a semnelor clinice,
S-a demonstrat că imunitatea se instalează la 1 săptămână după
prima vaccinare, în ceea ce priveşte
rinotraheita, caliciviroza,
_ _

                                
                                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
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Public Assessment Report Public Assessment Report English 09-03-2021
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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
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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 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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