BTVPUR

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

bluetongue-virus serotype-1 antigen, bluetongue virus serotype 8 antigen

Available from:

Boehringer Ingelheim Vetmedica GmbH

ATC code:

QI04AA02, QI02AA08

INN (International Name):

inactivated vaccine against bluetongue virus serotypes 1 and 8

Therapeutic group:

Sheep; Cattle

Therapeutic area:

Imunologija

Therapeutic indications:

SheepActive imunizacijo ovc in goveda (za preprečevanje viraemia in za zmanjšanje kliničnih znakov, ki jih povzroča bolezen modrikastega jezika virus serotypes 1, 2, 4 in/ ali 8 (kombinacija največ 2 serotypes), aktivno imunizacijo ovc in goveda (za preprečevanje viraemia in za zmanjšanje kliničnih znakov, ki jih povzroča bolezen modrikastega jezika virus serotypes 1,2, 4 in/ ali 8 (kombinacija največ 2 serotypes), aktivno imunizacijo ovc za preprečevanje viraemia in za zmanjšanje kliničnih znakov, ki jih povzroča bolezen modrikastega jezika virus serotypes 1, 2, 4 in/ali 8 (kombinacija največ 2 serotypes). CattleActive imunizacijo goveda za preprečevanje viraemia zaradi bolezni modrikastega jezika virus serotip 1, 2, 4 in/ ali 8, in za zmanjšanje kliničnih znakov, ki jih povzroča bolezen modrikastega jezika virus serotypes, ko spremljamo v tem vrst: serotip 1, 4 in / ali 8 (kombinacija največ 2 serotypes). Aktivno imunizacijo goveda za preprečevanje viraemia zaradi bolezni modrikastega jezika virus serotip 1, 2, 4 in/ ali 8, in za zmanjšanje kliničnih znakov, ki jih povzroča bolezen modrikastega jezika virus serotypes, ko spremljamo v tem vrst: serotip 1, 4 in / ali 8 (kombinacija največ 2 serotypes). Aktivno imunizacijo ovc in goveda (za preprečevanje viraemia in za zmanjšanje kliničnih znakov, ki jih povzroča bolezen modrikastega jezika virus serotypes 1, 2, 4 in/ali 8 (kombinacija največ 2 serotypes).

Product summary:

Revision: 12

Authorization status:

Pooblaščeni

Authorization date:

2010-12-17

Patient Information leaflet

                                18
B. NAVODILO ZA UPORABO
19
NAVODILO ZA UPORABO
BTVPUR SUSPENZIJA ZA INJICIRANJE ZA OVCE IN GOVEDO
1.
IME IN NASLOV IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM TER
PROIZVAJALEC ZDRAVILA, ODGOVOREN ZA SPROŠČANJE SERIJ, ČE STA
RAZLIČNA
Imetnik dovoljenja za promet z zdravilom:
Boehringer Ingelheim Vetmedica GmbH
55216 Ingelheim/Rhein
NEMČIJA
Proizvajalec, odgovoren za sproščanje serij:
Boehringer Ingelheim Animal Health France SCS
Laboratory of Lyon Porte des Alpes
Rue de l’Aviation,
69800 Saint-Priest
Francija
2.
IME ZDRAVILA ZA UPORABO V VETERINARSKI MEDICINI
BTVPUR suspenzija za injiciranje za ovce in govedo
3.
NAVEDBA UČINKOVIN(E) IN DRUGE(IH) SESTAVIN
Vsak odmerek (1 ml) vsebuje:
ZDRAVILNE UČINKOVINE*
:
Inaktiviran virus bolezni modrikastega jezika (BTV) ........... ≥
sev specifični nivo (log
10
pikslov)**
* Največ dva različna inaktivirana serotipa virusa bolezni
modrikastega jezika
(**)Sev-specifični
nivo
(**) Vsebnost antigena
(VP2 protein) z
imunološkimi metodami
BTV1
1.9 log10 pikslov/ml
BTV2
1.82 log10 pikslov/ml
BTV4
1.86 log10 pikslov/ml
BTV8
2.12 log10 pikslov/ml
Končni potrditveni test jakosti je seronevtralizacijski test pri
podganah ob sprostitvi serije.
Končni potrditveni test jakosti je seronevtralizacijski test pri
podganah ob sprostitvi serije.
DODATKI:
Al
3+
(kot hidroksid)
2,7 mg
saponin
30 HU**
(
**
)
Hemolizne enote
Tip seva (največ dva seva) vključen v končno zdravilo, bo izbran
glede na epidemiološko situacijo ob
času proizvodnje cepiva in bo naveden na ovojnini.
Videz: homogen mlečno bel.
20
4.
INDIKACIJA(E)
Aktivna imunizacija ovac proti virusu bolezni modrikastega jezika,
serotip 1, 2, 4 in/ali 8, za
preprečitev viremije* in zmanjšanje kliničnih znakov (kombinacija
največ dveh različnih serotipov). .
Aktivna imunizacija goveda proti virusu bolezni modrikastega jezika,
serotip 1, 2, 4 in/ali 8, za
preprečitev viremije* in zmanjšanje kliničnih znakov povzročenih s
serotipi 1, 4 in/ali 8 (kombinacija
največ dveh različnih serotipov).
*pod stopnjo detekc
                                
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Summary of Product characteristics

                                1
PRILOGA I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
                                
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Patient Information leaflet Patient Information leaflet Bulgarian 27-10-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 27-10-2020
Public Assessment Report Public Assessment Report Bulgarian 18-10-2018
Patient Information leaflet Patient Information leaflet Spanish 27-10-2020
Public Assessment Report Public Assessment Report Spanish 18-10-2018
Patient Information leaflet Patient Information leaflet Czech 27-10-2020
Public Assessment Report Public Assessment Report Czech 18-10-2018
Patient Information leaflet Patient Information leaflet Danish 27-10-2020
Public Assessment Report Public Assessment Report Danish 18-10-2018
Patient Information leaflet Patient Information leaflet German 27-10-2020
Public Assessment Report Public Assessment Report German 18-10-2018
Patient Information leaflet Patient Information leaflet Estonian 27-10-2020
Public Assessment Report Public Assessment Report Estonian 18-10-2018
Patient Information leaflet Patient Information leaflet Greek 27-10-2020
Public Assessment Report Public Assessment Report Greek 18-10-2018
Patient Information leaflet Patient Information leaflet English 27-10-2020
Public Assessment Report Public Assessment Report English 18-10-2018
Patient Information leaflet Patient Information leaflet French 27-10-2020
Public Assessment Report Public Assessment Report French 18-10-2018
Patient Information leaflet Patient Information leaflet Italian 27-10-2020
Public Assessment Report Public Assessment Report Italian 18-10-2018
Patient Information leaflet Patient Information leaflet Latvian 27-10-2020
Public Assessment Report Public Assessment Report Latvian 18-10-2018
Patient Information leaflet Patient Information leaflet Lithuanian 27-10-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 27-10-2020
Public Assessment Report Public Assessment Report Lithuanian 18-10-2018
Patient Information leaflet Patient Information leaflet Hungarian 27-10-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 27-10-2020
Public Assessment Report Public Assessment Report Hungarian 18-10-2018
Patient Information leaflet Patient Information leaflet Maltese 27-10-2020
Public Assessment Report Public Assessment Report Maltese 18-10-2018
Patient Information leaflet Patient Information leaflet Dutch 27-10-2020
Public Assessment Report Public Assessment Report Dutch 18-10-2018
Patient Information leaflet Patient Information leaflet Polish 27-10-2020
Public Assessment Report Public Assessment Report Polish 18-10-2018
Patient Information leaflet Patient Information leaflet Portuguese 27-10-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 27-10-2020
Public Assessment Report Public Assessment Report Portuguese 18-10-2018
Patient Information leaflet Patient Information leaflet Romanian 27-10-2020
Public Assessment Report Public Assessment Report Romanian 18-10-2018
Patient Information leaflet Patient Information leaflet Slovak 27-10-2020
Public Assessment Report Public Assessment Report Slovak 18-10-2018
Patient Information leaflet Patient Information leaflet Finnish 27-10-2020
Public Assessment Report Public Assessment Report Finnish 18-10-2018
Patient Information leaflet Patient Information leaflet Swedish 27-10-2020
Public Assessment Report Public Assessment Report Swedish 18-10-2018
Patient Information leaflet Patient Information leaflet Norwegian 27-10-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 27-10-2020
Patient Information leaflet Patient Information leaflet Icelandic 27-10-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 27-10-2020
Patient Information leaflet Patient Information leaflet Croatian 27-10-2020
Public Assessment Report Public Assessment Report Croatian 18-10-2018

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