Bexsero

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

външна мембрана мехурчета от менингококк група B (щам 98/254 NC), рекомбинантный менингококк група в fHbp на синтеза на белтъци, рекомбинантен менингококк група B нада протеин, рекомбинантный менингококк група в NHBA синтеза на протеини

Available from:

GSK Vaccines S.r.l.

ATC code:

J07AH09

INN (International Name):

meningococcal group B Vaccine (rDNA, component, adsorbed)

Therapeutic group:

Менингококови ваксини

Therapeutic area:

Менингит, менингококов

Therapeutic indications:

Активна имунизация срещу инвазивно заболяване, причинено от щамове Neisseria meningitidis серогрупа-В.

Product summary:

Revision: 33

Authorization status:

упълномощен

Authorization date:

2013-01-13

Patient Information leaflet

                                32
Б. ЛИСТОВКА
33
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
BEXSERO ИНЖЕКЦИОННА СУСПЕНЗИЯ В
ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
Адсорбирана ваксина срещу
менингококи група B (рДНК, компонентна)
(Meningococcal group B Vaccine (rDNA, component, adsorbed))
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ТОВА ЛЕКАРСТВО ДА БЪДЕ
ПРИЛОЖЕНО НА ВАС
ИЛИ НА ДЕТЕТО ВИ, ТЪЙ КАТО ТЯ СЪДЪРЖА
ВАЖНА ЗА ВАС ИЛИ ЗА ВАШЕТО ДЕТЕ
ИНФОРМАЦИЯ.
-
Запазете тази листовка. Може да се
наложи да я прочетете отново.
-
Ако имате някакви допълнителни
въпроси, попитайте Вашия лекар или
медицинска сестра.
-
Тази ваксина е предписана лично на Вас
или на Вашето дете.
-
Ако получите някакви нежелани
реакции, уведомете Вашия лекар или
медицинска
сестра. Това включва и всички възможни
нежелани реакции, неописани в тази
листовка.
Вижте точка 4.
КАКВО СЪДЪРЖА ТАЗИ ЛИСТОВКА:
1.
Какво представлява Bexsero и за какво се
използва
2.
Какво трябва да знаете, преди Вие или
Вашето дете да получите Bexsero
3.
Как да използвате Bexsero
4.
Възможни нежелани реакции
5.
Как да съхранявате Bexsero
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА BEXSERO И ЗА КАКВО СЕ
ИЗПОЛЗВА
Bexsero е ваксина срещу менингок
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Bexsero инжекционна суспензия в
предварително напълнена спринцовка
Адсорбирана ваксина срещу
менингококи група B (рДНК, компонентна)
(Meningococcal group B Vaccine (rDNA, component, adsorbed))
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Една доза (0,5 ml) съдържа:
Рекомбинантен NHBA фузионен протеин на
_Neisseria meningitidis_
група B
1, 2, 3
(Recombinant
_Neisseria meningitidis_
group B NHBA fusion
protein
1, 2, 3
)
50 микрограма
Рекомбинантен NadA протеин на
_Neisseria meningitidis_
група B
1, 2, 3
(Recombinant
_Neisseria meningitidis _
group B NadA protein
1, 2, 3
)
50 микрограма
Рекомбинантен fHbp фузионен протеин на
_Neisseria meningitidis_
група B
1, 2, 3
(Recombinant
_Neisseria meningitidis_
group B fHbp fusion protein
1, 2, 3
)
50 микрограма
Везикули от външната мембрана (OMV) на
_Neisseria meningitidis_
група B
щам NZ98/254, измерени като количество общ
протеин, съдържащ PorA
P1.4
2
(Outer membrane vesicles (OMV) from
_Neisseria meningitidis _
group B
strain NZ98/254 measured as amount of total protein containing the
PorA P1.4
2
)
25 микрограма
1
произведени в клетки на
_E. coli_
чрез рекомбинантна ДНК технология
2
адсорбирани върху алуминиев
хидроксид (0,5 mg Al
3+
)
3
NHBA (Neisserial Heparin Binding Antigen [хепарин
свързващ антиген на
_Neisseria_
]),
NadA (
_Neisseria_
adhesin A [адхезин А на
_Neisseria_
]), fHbp (factor H binding protein
[фактор H свързващ протеин])
За п
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 23-05-2023
Public Assessment Report Public Assessment Report Spanish 11-07-2018
Patient Information leaflet Patient Information leaflet Czech 23-05-2023
Public Assessment Report Public Assessment Report Czech 11-07-2018
Patient Information leaflet Patient Information leaflet Danish 23-05-2023
Public Assessment Report Public Assessment Report Danish 11-07-2018
Patient Information leaflet Patient Information leaflet German 23-05-2023
Public Assessment Report Public Assessment Report German 11-07-2018
Patient Information leaflet Patient Information leaflet Estonian 23-05-2023
Public Assessment Report Public Assessment Report Estonian 11-07-2018
Patient Information leaflet Patient Information leaflet Greek 23-05-2023
Public Assessment Report Public Assessment Report Greek 11-07-2018
Patient Information leaflet Patient Information leaflet English 23-05-2023
Public Assessment Report Public Assessment Report English 11-07-2018
Patient Information leaflet Patient Information leaflet French 23-05-2023
Public Assessment Report Public Assessment Report French 11-07-2018
Patient Information leaflet Patient Information leaflet Italian 23-05-2023
Public Assessment Report Public Assessment Report Italian 11-07-2018
Patient Information leaflet Patient Information leaflet Latvian 23-05-2023
Public Assessment Report Public Assessment Report Latvian 11-07-2018
Patient Information leaflet Patient Information leaflet Lithuanian 23-05-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 23-05-2023
Public Assessment Report Public Assessment Report Lithuanian 11-07-2018
Patient Information leaflet Patient Information leaflet Hungarian 23-05-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 23-05-2023
Public Assessment Report Public Assessment Report Hungarian 11-07-2018
Patient Information leaflet Patient Information leaflet Maltese 23-05-2023
Public Assessment Report Public Assessment Report Maltese 11-07-2018
Patient Information leaflet Patient Information leaflet Dutch 23-05-2023
Public Assessment Report Public Assessment Report Dutch 11-07-2018
Patient Information leaflet Patient Information leaflet Polish 23-05-2023
Public Assessment Report Public Assessment Report Polish 11-07-2018
Patient Information leaflet Patient Information leaflet Portuguese 23-05-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 23-05-2023
Public Assessment Report Public Assessment Report Portuguese 11-07-2018
Patient Information leaflet Patient Information leaflet Romanian 23-05-2023
Public Assessment Report Public Assessment Report Romanian 11-07-2018
Patient Information leaflet Patient Information leaflet Slovak 23-05-2023
Public Assessment Report Public Assessment Report Slovak 11-07-2018
Patient Information leaflet Patient Information leaflet Slovenian 23-05-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 23-05-2023
Public Assessment Report Public Assessment Report Slovenian 11-07-2018
Patient Information leaflet Patient Information leaflet Finnish 23-05-2023
Public Assessment Report Public Assessment Report Finnish 11-07-2018
Patient Information leaflet Patient Information leaflet Swedish 23-05-2023
Public Assessment Report Public Assessment Report Swedish 11-07-2018
Patient Information leaflet Patient Information leaflet Norwegian 23-05-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 23-05-2023
Patient Information leaflet Patient Information leaflet Icelandic 23-05-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 23-05-2023
Patient Information leaflet Patient Information leaflet Croatian 23-05-2023
Public Assessment Report Public Assessment Report Croatian 11-07-2018

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