Dengvaxia

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

chimeric yellow fever dengue virus serotype 1 (live, attenuated), chimeric yellow fever dengue virus serotype 2 (live, attenuated), chimeric yellow fever dengue virus serotype 3 (live, attenuated), chimeric yellow fever dengue virus serotype 4 (live, attenuated)

Available from:

Sanofi Pasteur

ATC code:

J07BX

INN (International Name):

dengue tetravalent vaccine (live, attenuated)

Therapeutic group:

Ваксини

Therapeutic area:

Денга

Therapeutic indications:

Dengvaxia is indicated for the prevention of dengue disease caused by dengue virus serotypes 1, 2, 3 and 4 in individuals 6 to 45 years of age with test-confirmed previous dengue infection (see sections 4. 2, 4. 4 и 4. Използването на Dengvaxia трябва да бъде в съответствие с официалните препоръки.

Product summary:

Revision: 5

Authorization status:

упълномощен

Authorization date:

2018-12-12

Patient Information leaflet

                                49
Б. ЛИСТОВКА
50
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
DENGVAXIA ПРАХ И РАЗТВОРИТЕЛ ЗА
ИНЖЕКЦИОННА СУСПЕНЗИЯ В
ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
четиривалентна ваксина срещу денга
(жива, атенюирана)
[dengue tetravalent vaccine (live, attenuated)]
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ВИЕ ИЛИ ВАШЕТО ДЕТЕ БЪДЕТЕ
ВАКСИНИРАНИ,
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 Вашето дете. Не я преотстъпвайте
на други
хора.
•
Ако Вие или Вашето дете получите
някакви нежелани реакции, уведомете
Вашия лекар,
фармацевт или медицинска сестра. Това
включва и всички възможни нежелани
реакции,
неописани в тази листовка. Вижте точка
4.
КАКВО СЪДЪРЖА ТАЗИ ЛИСТОВКА
1.
Какво представлява Dengvaxia и за какво се
използва
2.
Какво трябва да знаете, преди Вие или
Вашето дете използвате Dengvaxia
3.
Как да използвате Dengvaxia
4.
Възможни нежелани реакции
5.
Как да съхранявате Dengvaxia
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА DENGVAXIA 
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Dengvaxia прах и разтворител за
инжекционна суспензия в
предварително напълнена
спринцовка
Четиривалентна ваксина срещу денга
(жива, атенюирана)
[dengue tetravalent vaccine (live, attenuated)]
2
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
След реконституиране, една доза (0,5 ml)
съдържа:
Химерен жълта треска/денга вирус
серотип 1
*
(жив, атенюиран) ........ 4,5 - 6,0 log
10
CCID
50
/доза
**
[Chimeric yellow fever dengue virus serotype 1*(live, attenuated)]
Химерен жълта треска/денга вирус
серотип 2*(жив, атенюиран) ....... 4,5 – 6,0 log
10
CCID
50
/доза
**
[Chimeric yellow fever dengue virus serotype 2*(live, attenuated)]
Химерен жълта треска/денга вирус
серотип 3*(жив, атенюиран) ....... 4,5 – 6,0 log
10
CCID
50
/доза
**
[Chimeric yellow fever dengue virus serotype 3*(live, attenuated)]
Химерен жълта треска/денга вирус
серотип 4*(жив, атенюиран) ....... 4,5 – 6,0 log
10
CCID
50
/доза
**
[Chimeric yellow fever dengue virus serotype 4*(live, attenuated)]
*
Произведен във Vero клетки чрез
рекомбинантна ДНК технология. Този
продукт съдържа
генетично модифицирани организми
(ГМО).
**
CCID
50
: 50% инфекциозна доза за клетъчна
култура.
Помощни вещества с известно действие:
Една доза (0,5 ml) съдържа 41 микрограма
фенилаланин и 9,38 милиграма сорбитол.
За пълния списък на помо
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 04-01-2024
Public Assessment Report Public Assessment Report Spanish 26-01-2022
Patient Information leaflet Patient Information leaflet Czech 04-01-2024
Public Assessment Report Public Assessment Report Czech 26-01-2022
Patient Information leaflet Patient Information leaflet Danish 04-01-2024
Public Assessment Report Public Assessment Report Danish 26-01-2022
Patient Information leaflet Patient Information leaflet German 04-01-2024
Public Assessment Report Public Assessment Report German 26-01-2022
Patient Information leaflet Patient Information leaflet Estonian 04-01-2024
Public Assessment Report Public Assessment Report Estonian 26-01-2022
Patient Information leaflet Patient Information leaflet Greek 04-01-2024
Public Assessment Report Public Assessment Report Greek 26-01-2022
Patient Information leaflet Patient Information leaflet English 04-01-2024
Public Assessment Report Public Assessment Report English 26-01-2022
Patient Information leaflet Patient Information leaflet French 04-01-2024
Public Assessment Report Public Assessment Report French 26-01-2022
Patient Information leaflet Patient Information leaflet Italian 04-01-2024
Public Assessment Report Public Assessment Report Italian 26-01-2022
Patient Information leaflet Patient Information leaflet Latvian 04-01-2024
Public Assessment Report Public Assessment Report Latvian 26-01-2022
Patient Information leaflet Patient Information leaflet Lithuanian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 04-01-2024
Public Assessment Report Public Assessment Report Lithuanian 26-01-2022
Patient Information leaflet Patient Information leaflet Hungarian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 04-01-2024
Public Assessment Report Public Assessment Report Hungarian 26-01-2022
Patient Information leaflet Patient Information leaflet Maltese 04-01-2024
Public Assessment Report Public Assessment Report Maltese 26-01-2022
Patient Information leaflet Patient Information leaflet Dutch 04-01-2024
Public Assessment Report Public Assessment Report Dutch 26-01-2022
Patient Information leaflet Patient Information leaflet Polish 04-01-2024
Public Assessment Report Public Assessment Report Polish 26-01-2022
Patient Information leaflet Patient Information leaflet Portuguese 04-01-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 04-01-2024
Public Assessment Report Public Assessment Report Portuguese 26-01-2022
Patient Information leaflet Patient Information leaflet Romanian 04-01-2024
Public Assessment Report Public Assessment Report Romanian 26-01-2022
Patient Information leaflet Patient Information leaflet Slovak 04-01-2024
Public Assessment Report Public Assessment Report Slovak 26-01-2022
Patient Information leaflet Patient Information leaflet Slovenian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 04-01-2024
Public Assessment Report Public Assessment Report Slovenian 26-01-2022
Patient Information leaflet Patient Information leaflet Finnish 04-01-2024
Public Assessment Report Public Assessment Report Finnish 26-01-2022
Patient Information leaflet Patient Information leaflet Swedish 04-01-2024
Public Assessment Report Public Assessment Report Swedish 26-01-2022
Patient Information leaflet Patient Information leaflet Norwegian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 04-01-2024
Patient Information leaflet Patient Information leaflet Icelandic 04-01-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 04-01-2024
Patient Information leaflet Patient Information leaflet Croatian 04-01-2024
Public Assessment Report Public Assessment Report Croatian 26-01-2022

View documents history