Jakavi

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

руксолитиниб (като фосфат)

Available from:

Novartis Europharm Limited

ATC code:

L01EJ01

INN (International Name):

ruxolitinib

Therapeutic group:

Антинеопластични средства

Therapeutic area:

Myeloproliferative Disorders; Polycythemia Vera; Graft vs Host Disease

Therapeutic indications:

Myelofibrosis (MF)Jakavi is indicated for the treatment of disease related splenomegaly or symptoms in adult patients with primary myelofibrosis (also known as chronic idiopathic myelofibrosis), post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis. Полицитемия Вера (PX)Jakavi е показан за лечение на възрастни пациенти с полицитемия вера, които са резистентни или с непоносимост към гидроксимочевины. Graft versus host disease (GvHD)Jakavi is indicated for the treatment of patients aged 12 years and older with acute graft versus host disease or chronic graft versus host disease who have inadequate response to corticosteroids or other systemic therapies (see section 5.

Product summary:

Revision: 28

Authorization status:

упълномощен

Authorization date:

2012-08-23

Patient Information leaflet

                                69
Б. ЛИСТОВКА
70
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПАЦИЕНТА
JAKAVI 5 MG ТАБЛЕТКИ
JAKAVI 10 MG ТАБЛЕТКИ
JAKAVI 15 MG ТАБЛЕТКИ
JAKAVI 20 MG ТАБЛЕТКИ
руксолитиниб (ruxolitinib)
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ЗАПОЧНЕТЕ ДА ПРИЕМАТЕ ТОВА
ЛЕКАРСТВО,
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 или
фармацевт.
-
Това лекарство е предписано лично на
Вас. Не го преотстъпвайте на други
хора. То може
да им навреди, независимо че
признаците на тяхното заболяване са
същите като Вашите.
-
Ако получите някакви нежелани
реакции, уведомете Вашия лекар или
фармацевт. Това
включва и всички възможни нежелани
реакции, неописани в тази листовка.
Вижте
точка 4.
КАКВО СЪДЪРЖА ТАЗИ ЛИСТОВКА
1.
Какво представлява Jakavi и за какво се
използва
2.
Какво трябва да знаете, преди да
приемете Jakavi
3.
Как да приемате Jakavi
4.
Възможни нежелани реакции
5.
Как да съхранявате Jakavi
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА JAKAVI И ЗА КАКВО СЕ
ИЗПОЛЗВА
Jakavi съдържа активното вещество
руксолитиниб.
Jakavi се използва за лечение н
                                
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Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Jakavi 5 mg таблетки
Jakavi 10 mg таблетки
Jakavi 15 mg таблетки
Jakavi 20 mg таблетки
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Jakavi 5 mg таблетки
Всяка таблетка съдържа 5 mg
руксолитиниб (ruxolitinib) (като фосфат).
_Помощно вещество с известно действие
_
Всяка таблетка съдържа 71,45 mg лактоза
монохидрат.
Jakavi 10 mg таблетки
Всяка таблетка съдържа 10 mg
руксолитиниб (ruxolitinib) (като фосфат).
_Помощно вещество с известно действие
_
Всяка таблетка съдържа 142,90 mg лактоза
монохидрат.
Jakavi 15 mg таблетки
Всяка таблетка съдържа 15 mg
руксолитиниб (ruxolitinib) (като фосфат).
_Помощно вещество с известно действие
_
Всяка таблетка съдържа 214,35 mg лактоза
монохидрат.
Jakavi 20 mg таблетки
Всяка таблетка съдържа 20 mg
руксолитиниб (ruxolitinib) (като фосфат).
_Помощно вещество с известно действие
_
Всяка таблетка съдържа 285,80 mg лактоза
монохидрат.
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Таблетка
Jakavi 5 mg таблетки
Бяла до почти бяла кръгла таблетка, с
диаметър приблизително 7,5 mm, с
вдлъбнато релефно
означение „NVR“ от едната страна и
„L5“ от другата.
Jakavi 10 mg таблетки
Бяла до почти бяла кръг
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 18-05-2022
Public Assessment Report Public Assessment Report Spanish 18-05-2022
Patient Information leaflet Patient Information leaflet Czech 18-05-2022
Public Assessment Report Public Assessment Report Czech 18-05-2022
Patient Information leaflet Patient Information leaflet Danish 18-05-2022
Public Assessment Report Public Assessment Report Danish 18-05-2022
Patient Information leaflet Patient Information leaflet German 18-05-2022
Public Assessment Report Public Assessment Report German 18-05-2022
Patient Information leaflet Patient Information leaflet Estonian 18-05-2022
Public Assessment Report Public Assessment Report Estonian 18-05-2022
Patient Information leaflet Patient Information leaflet Greek 18-05-2022
Public Assessment Report Public Assessment Report Greek 18-05-2022
Patient Information leaflet Patient Information leaflet English 18-05-2022
Public Assessment Report Public Assessment Report English 18-05-2022
Patient Information leaflet Patient Information leaflet French 18-05-2022
Public Assessment Report Public Assessment Report French 18-05-2022
Patient Information leaflet Patient Information leaflet Italian 18-05-2022
Public Assessment Report Public Assessment Report Italian 18-05-2022
Patient Information leaflet Patient Information leaflet Latvian 18-05-2022
Public Assessment Report Public Assessment Report Latvian 18-05-2022
Patient Information leaflet Patient Information leaflet Lithuanian 18-05-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 18-05-2022
Public Assessment Report Public Assessment Report Lithuanian 18-05-2022
Patient Information leaflet Patient Information leaflet Hungarian 18-05-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 18-05-2022
Public Assessment Report Public Assessment Report Hungarian 18-05-2022
Patient Information leaflet Patient Information leaflet Maltese 18-05-2022
Public Assessment Report Public Assessment Report Maltese 18-05-2022
Patient Information leaflet Patient Information leaflet Dutch 18-05-2022
Public Assessment Report Public Assessment Report Dutch 18-05-2022
Patient Information leaflet Patient Information leaflet Polish 18-05-2022
Public Assessment Report Public Assessment Report Polish 18-05-2022
Patient Information leaflet Patient Information leaflet Portuguese 18-05-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 18-05-2022
Public Assessment Report Public Assessment Report Portuguese 18-05-2022
Patient Information leaflet Patient Information leaflet Romanian 18-05-2022
Public Assessment Report Public Assessment Report Romanian 18-05-2022
Patient Information leaflet Patient Information leaflet Slovak 18-05-2022
Public Assessment Report Public Assessment Report Slovak 18-05-2022
Patient Information leaflet Patient Information leaflet Slovenian 18-05-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 18-05-2022
Public Assessment Report Public Assessment Report Slovenian 18-05-2022
Patient Information leaflet Patient Information leaflet Finnish 18-05-2022
Public Assessment Report Public Assessment Report Finnish 18-05-2022
Patient Information leaflet Patient Information leaflet Swedish 18-05-2022
Public Assessment Report Public Assessment Report Swedish 18-05-2022
Patient Information leaflet Patient Information leaflet Norwegian 18-05-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 18-05-2022
Patient Information leaflet Patient Information leaflet Icelandic 18-05-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 18-05-2022
Patient Information leaflet Patient Information leaflet Croatian 18-05-2022
Public Assessment Report Public Assessment Report Croatian 18-05-2022

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