ProteqFlu

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

Вирус PDS 2242 вирусът / вирус Vcp1529 / Vcp1533 вирус / vCP3011

Available from:

Boehringer Ingelheim Vetmedica GmbH

ATC code:

QI05AD02

INN (International Name):

Equine influenza vaccine (live recombinant)

Therapeutic group:

Коне

Therapeutic area:

Имуномодулатори, живи вирусни ваксини вируса на грипа коне

Therapeutic indications:

Активна имунизация на коне на възраст 4 месеца или повече срещу грип от коне за намаляване на клиничните признаци и отделяне на вируси след инфекция.

Product summary:

Revision: 14

Authorization status:

упълномощен

Authorization date:

2003-03-06

Patient Information leaflet

                                13
B. ЛИСТОВКА
14
ЛИСТОВКА
PROTEQFLU ИНЖЕКЦИОННА СУСПЕНЗИЯ ЗА КОНЕ
1.
ИМЕ И ПОСТОЯНEН АДРЕС НА ПРИТЕЖАТЕЛЯ
НА ЛИЦЕНЗА ЗА УПОТРЕБА
И НА ПРОИЗВОДИТЕЛЯ, АКО ТЕ СА РАЗЛИЧНИ
Притежател на лиценза за употреба:
Boehringer Ingelheim Vetmedica GmbH
55216 Ingelheim/Rhein
ГЕРМАНИЯ
Производител, отговорен за
освобождаване на партидата:
Boehringer Ingelheim Animal Health France SCS
Laboratoire Porte des Alpes
Rue de l'Aviation
69800 Saint Priest
FRANCE
2.
НАИМЕНОВАНИЕ НА
ВЕТЕРИНАРНОМЕДИЦИНСКИЯ ПРОДУКТ
ProteqFlu
Инжекционна суспензия за коне.
3.
СЪДЪРЖАНИЕ НА АКТИВНИТЕ СУБСТАНЦИ И
ЕКСЦИПИЕНТИТЕ
Една доза от 1 ml съдържа:
АКТИВНИ СУБСТАНЦИИ:
Influenza A/eq/Ohio/03[H
3
N
8
] рекомбинантен canarypox вирус (vCP2242)
..........................................................................................................................................
≥ 5.3 log10 FAID
50
*
Influenza A/eq/Richmond/1/07 [H
3
N
8
] рекомбинантен canarypox вирус (vCP3011) ... ≥
5.3 log10 FAID
50
* vCP съдържание проверено чрез общия FAID
50
( отчетени по флуоресцентен метод
инфекциозни дози 50%) и съотношение
между qPCR и vCP.
АДЖУВАНТ:
Carbomer
..................................................................................................................................................
4 mg.
4.
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Активна имунизация на коне след
навършване на 4 месечна възраст срещу
инфлуенца за
редуциране на клиничните признаци и
за прек
                                
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Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
НАИМЕНОВАНИЕ НА
ВЕТЕРИНАРНОМЕДИЦИНСКИЯ ПРОДУКТ
ProteqFlu инжекционна суспензия за коне
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Една доза от 1ml съдържа:
АКТИВНИ СУБСТАНЦИИ:
Influenza A/eq/Ohio/03 [H
3
N
8
] рекомбинантен вирус canarypox (vCP2242)
..........................................................................................................................................
≥ 5.3 log10 FAID
50
*
Influenza A/eq/Richmond/1/07[H
3
N
8
] рекомбинантен вирус canarypox (vCP3011) .. ≥ 5.3
log10 FAID
50
*
*vCP съдържание проверено чрез общия FAID
50
(флуоресцентен анализ на инфекциозна
доза
50%) и съотношение между qPCR и vCP
АДЖУВАНТ:
Carbomer
.................................................................................................................................................
4 mg.
ЕКСЦИПИЕНТИ:
За пълен списък на ексципиентите, виж
т. 6.1.
3.
ФАРМАЦЕВТИЧНА ФОРМА
Инжекционна суспензия.
4.
КЛИНИЧНИ ДАННИ
4.1.
ВИДОВЕ ЖИВОТНИ, ЗА КОИТО Е
ПРЕДНАЗНАЧЕН ВМП
Коне.
4.2.
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ, ОПРЕДЕЛЕНИ ЗА
ОТДЕЛНИТЕ ВИДОВЕ ЖИВОТНИ
Активна имунизация на коне след 4
месечна възраст срещу грип за
редуциране на клиничните
признаци и вирусната екскреция след
заразяване.
Изграждане на имунитет: 14 дни след
начална ваксинация.
Продължителност на имунитета при
прилагане на ваксинална
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 23-11-2020
Public Assessment Report Public Assessment Report Spanish 17-10-2014
Patient Information leaflet Patient Information leaflet Czech 23-11-2020
Public Assessment Report Public Assessment Report Czech 17-10-2014
Patient Information leaflet Patient Information leaflet Danish 23-11-2020
Public Assessment Report Public Assessment Report Danish 17-10-2014
Patient Information leaflet Patient Information leaflet German 23-11-2020
Public Assessment Report Public Assessment Report German 17-10-2014
Patient Information leaflet Patient Information leaflet Estonian 23-11-2020
Public Assessment Report Public Assessment Report Estonian 17-10-2014
Patient Information leaflet Patient Information leaflet Greek 23-11-2020
Public Assessment Report Public Assessment Report Greek 17-10-2014
Patient Information leaflet Patient Information leaflet English 23-11-2020
Public Assessment Report Public Assessment Report English 17-10-2014
Patient Information leaflet Patient Information leaflet French 23-11-2020
Public Assessment Report Public Assessment Report French 17-10-2014
Patient Information leaflet Patient Information leaflet Italian 23-11-2020
Public Assessment Report Public Assessment Report Italian 17-10-2014
Patient Information leaflet Patient Information leaflet Latvian 23-11-2020
Public Assessment Report Public Assessment Report Latvian 17-10-2014
Patient Information leaflet Patient Information leaflet Lithuanian 23-11-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 23-11-2020
Public Assessment Report Public Assessment Report Lithuanian 17-10-2014
Patient Information leaflet Patient Information leaflet Hungarian 23-11-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 23-11-2020
Public Assessment Report Public Assessment Report Hungarian 17-10-2014
Patient Information leaflet Patient Information leaflet Maltese 23-11-2020
Public Assessment Report Public Assessment Report Maltese 17-10-2014
Patient Information leaflet Patient Information leaflet Dutch 23-11-2020
Public Assessment Report Public Assessment Report Dutch 17-10-2014
Patient Information leaflet Patient Information leaflet Polish 23-11-2020
Public Assessment Report Public Assessment Report Polish 17-10-2014
Patient Information leaflet Patient Information leaflet Portuguese 23-11-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 23-11-2020
Public Assessment Report Public Assessment Report Portuguese 17-10-2014
Patient Information leaflet Patient Information leaflet Romanian 23-11-2020
Public Assessment Report Public Assessment Report Romanian 17-10-2014
Patient Information leaflet Patient Information leaflet Slovak 23-11-2020
Public Assessment Report Public Assessment Report Slovak 17-10-2014
Patient Information leaflet Patient Information leaflet Slovenian 23-11-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 23-11-2020
Public Assessment Report Public Assessment Report Slovenian 17-10-2014
Patient Information leaflet Patient Information leaflet Finnish 23-11-2020
Public Assessment Report Public Assessment Report Finnish 17-10-2014
Patient Information leaflet Patient Information leaflet Swedish 23-11-2020
Public Assessment Report Public Assessment Report Swedish 17-10-2014
Patient Information leaflet Patient Information leaflet Norwegian 23-11-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 23-11-2020
Patient Information leaflet Patient Information leaflet Icelandic 23-11-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 23-11-2020
Patient Information leaflet Patient Information leaflet Croatian 23-11-2020
Public Assessment Report Public Assessment Report Croatian 17-10-2014

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