Vaxneuvance

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

pneumococcal polysaccharide conjugate vaccine (adsorbed)

Available from:

Merck Sharp & Dohme B.V. 

ATC code:

J07AL02

INN (International Name):

pneumococcal polysaccharide conjugate vaccine (adsorbed)

Therapeutic group:

pneumococcus, purified polysaccharides antigen conjugated

Therapeutic area:

Пневмококови инфекции

Therapeutic indications:

Vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by Streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. Vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by Streptococcus pneumoniae in individuals 18 years of age and older. Вижте раздели 4. 4 и 5. 1 за информация относно защитата срещу специфични пневмококови серотипове. The use of Vaxneuvance should be in accordance with official recommendations.

Product summary:

Revision: 5

Authorization status:

упълномощен

Authorization date:

2021-12-13

Patient Information leaflet

                                39
Б. ЛИСТОВКА
40
Листовка: информация за потребителя
VAXNEUVANCE
инжекционна суспензия в
предварително напълнена спринцовка
Пневмококова полизахаридна конюгатна
ваксина
(15-
валентна
,
адсорбирана
)
[Pneumococcal polysaccharide conjugate vaccine (15
-
valent, adsorbed)]
Този лекарствен продукт подлежи на
допълнително наблюдение.
Това ще позволи бързото
установяване на нова информация
относно безопасността.
Можете да дадете своя принос като
съобщите всяка нежелана реакция,
която сте получили
Вие или Вашето дете
.
За начина на
съобщаване на нежелани реакции вижте
края на точка
4.
Прочетете внимателно цялата листовка,
преди да ваксинирате
себе си или Вашето дете
,
тъй като тя съдържа важна за Вас
информация.
•
Запазете тази листовка.
Може да се наложи
да я прочетете отново.
•
Ако имате някакви допълнителни
въпроси, попитайте Вашия лекар
,
фармацевт
или
медицинска сестра
.
•
Тази ваксина е предписана лично
на Вас
или на Вашето дете
.
Не я преотстъпвайте на
други хора.
•
Ако получите някакви нежелани реакции
,
уведомете Вашия
лекар
,
фармацевт
или
медицинска сестра.
Това включва и всички възможни
нежелани реакции, неописани в
тази листовка. Вижте т
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
Този лекарствен продукт подлежи на
допълнително наблюдение. Това ще
позволи бързото
установяване на нова информация
относно безопасността. От
медицинските специалисти се
изисква да съобщават всяка подозирана
нежелана реакция. За начина на
съобщаване на
нежелани реакции вижте точка
4.8
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Vaxneuvance
инжекционна суспензия в
предварително напълнена спринцовка
Пневмококова полизахаридна конюгатна
ваксина
(15-
валентна
,
адсорбирана
)
[
Pneumococcal polysaccharide conjugate vaccine (15
-
valent, adsorbed)
]
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
1
доза (0,5
ml) съдържа:
Пневмококов полизахариден серотип
1
1,2
(Pneumococcal polysaccharide serotype 1
1,2
)
2,0
микрограма
Пневмококов полизахариден серотип
3
1,2
(Pneumococcal polysaccharide serotype
3
1,2
)
2,0
микрограма
Пневмококов полизахариден серотип
4
1,2
(Pneumococcal polysaccharide serotype
4
1,2
)
2,0
микрограма
Пневмококов полизахариден серотип
5
1,2
(Pneumococcal polysaccharide serotype
5
1,2
)
2,0
микрограма
Пневмококов полизахариден серотип
6A
1,2
(Pneumococcal polysaccharide serotype
6A
1,2
)
2,0
микрограма
Пневмококов полизахариден серотип
6B
1,2
(Pneumococcal polysaccharide serotype
6B
1,2
)
4,0
микрограма
Пневмококов полизахариден серотип
7F
1,2
(Pneumococcal po
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 23-02-2024
Public Assessment Report Public Assessment Report Spanish 29-11-2022
Patient Information leaflet Patient Information leaflet Czech 23-02-2024
Public Assessment Report Public Assessment Report Czech 29-11-2022
Patient Information leaflet Patient Information leaflet Danish 23-02-2024
Public Assessment Report Public Assessment Report Danish 29-11-2022
Patient Information leaflet Patient Information leaflet German 23-02-2024
Public Assessment Report Public Assessment Report German 29-11-2022
Patient Information leaflet Patient Information leaflet Estonian 23-02-2024
Public Assessment Report Public Assessment Report Estonian 29-11-2022
Patient Information leaflet Patient Information leaflet Greek 23-02-2024
Public Assessment Report Public Assessment Report Greek 29-11-2022
Patient Information leaflet Patient Information leaflet English 23-02-2024
Public Assessment Report Public Assessment Report English 29-11-2022
Patient Information leaflet Patient Information leaflet French 23-02-2024
Public Assessment Report Public Assessment Report French 29-11-2022
Patient Information leaflet Patient Information leaflet Italian 23-02-2024
Public Assessment Report Public Assessment Report Italian 29-11-2022
Patient Information leaflet Patient Information leaflet Latvian 23-02-2024
Public Assessment Report Public Assessment Report Latvian 29-11-2022
Patient Information leaflet Patient Information leaflet Lithuanian 23-02-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 23-02-2024
Public Assessment Report Public Assessment Report Lithuanian 29-11-2022
Patient Information leaflet Patient Information leaflet Hungarian 23-02-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 23-02-2024
Public Assessment Report Public Assessment Report Hungarian 29-11-2022
Patient Information leaflet Patient Information leaflet Maltese 23-02-2024
Public Assessment Report Public Assessment Report Maltese 29-11-2022
Patient Information leaflet Patient Information leaflet Dutch 23-02-2024
Public Assessment Report Public Assessment Report Dutch 29-11-2022
Patient Information leaflet Patient Information leaflet Polish 23-02-2024
Public Assessment Report Public Assessment Report Polish 29-11-2022
Patient Information leaflet Patient Information leaflet Portuguese 23-02-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 23-02-2024
Public Assessment Report Public Assessment Report Portuguese 29-11-2022
Patient Information leaflet Patient Information leaflet Romanian 23-02-2024
Public Assessment Report Public Assessment Report Romanian 29-11-2022
Patient Information leaflet Patient Information leaflet Slovak 23-02-2024
Public Assessment Report Public Assessment Report Slovak 29-11-2022
Patient Information leaflet Patient Information leaflet Slovenian 23-02-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 23-02-2024
Public Assessment Report Public Assessment Report Slovenian 29-11-2022
Patient Information leaflet Patient Information leaflet Finnish 23-02-2024
Public Assessment Report Public Assessment Report Finnish 29-11-2022
Patient Information leaflet Patient Information leaflet Swedish 23-02-2024
Public Assessment Report Public Assessment Report Swedish 29-11-2022
Patient Information leaflet Patient Information leaflet Norwegian 23-02-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 23-02-2024
Patient Information leaflet Patient Information leaflet Icelandic 23-02-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 23-02-2024
Patient Information leaflet Patient Information leaflet Croatian 23-02-2024
Public Assessment Report Public Assessment Report Croatian 29-11-2022

View documents history