Azacitidine Celgene

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

азацитидин

Available from:

Celgene Europe BV

ATC code:

L01BC07

INN (International Name):

azacitidine

Therapeutic group:

Антинеопластични средства

Therapeutic area:

Myelodysplastic Syndromes; Leukemia, Myelomonocytic, Chronic; Leukemia, Myeloid, Acute

Therapeutic indications:

Azacitidine Celgene is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (HSCT) with:intermediate 2 and high-risk myelodysplastic syndromes (MDS) according to the International Prognostic Scoring System (IPSS),chronic myelomonocytic leukaemia (CMML) with 10 29 % marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (AML) with 20 30 % blasts and multi-lineage dysplasia, according to World Health Organisation (WHO) classification,AML with >30% marrow blasts according to the WHO classification.

Product summary:

Revision: 2

Authorization status:

Отменено

Authorization date:

2019-08-02

Patient Information leaflet

                                29
Б. ЛИСТОВКА
Лекарствен продукт с невалидно
разрешение за употреба
30
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
АЗАЦИТИДИН CELGENE 25 MG/ML ПРАХ ЗА
ИНЖЕКЦИОННА СУСПЕНЗИЯ
Азацитидин (azacitidine)
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ЗАПОЧНЕТЕ ДА ИЗПОЛЗВАТЕ 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,
фармацевт или
медицинска сестра.
-
Ако 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 Азацитидин Celgene и
за какво се използва
2.
Какво трябва да знаете, преди да
използвате Азацитидин Celgene
3.
Как да използвате Азацитидин Celgene
4.
Възможни нежелани реакции
5
Как да съхранявате Азацитидин Celgene
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА АЗАЦИТИДИН CELGENE И
ЗА КАКВО СЕ ИЗПОЛЗВА
КАКВО ПРЕДСТАВЛЯВА АЗАЦИТИДИН CELGENE
Азацитидин Celgene е противораково
средство, което принадлежи къ
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
Лекарствен продукт с невалидно
разрешение за употреба
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Азацитидин Celgene 25 mg/ml прах за
инжекционна суспензия
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Всеки флакон съдържа 100 mg азацитидин
(azacitidine). След разтваряне всеки
милилитър
суспензия съдържа 25 mg азaцитидин.
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Прах за инжекционна суспензия
Бял лиофилизиран прах
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Азацитидин Celgene е показан за лечение
на възрастни пациенти, които не са
подходящи за
трансплантация на хемопоетични
стволови клетки (
_Haematopoietic stem cell transplantation,_
HSCT), с:
•
миелодиспластични синдроми (
_Myelodysplastic syndromes, _
MDS) с междинен-2 и висок
риск
според Международната прогностична
точкова система (
_International Prognostic _
_Scoring System,_
IPSS),
•
хронична миеломоноцитна левкемия (
_Chronic Myelomonocytic Leukaemia, _
CMML)
с 10-29% костномозъчни бласти без
миелопролиферативно нарушение,
•
остра миелоидна левкемия (
_Acute Myeloid Leukaemia, _
AML) с 20-30% бласти и
мултилинейна дисплазия според
класификацията на Световната здравна
организация (СЗО),
•
AML с > 30% костномозъчн
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 04-08-2021
Public Assessment Report Public Assessment Report Spanish 04-08-2021
Patient Information leaflet Patient Information leaflet Czech 04-08-2021
Public Assessment Report Public Assessment Report Czech 04-08-2021
Patient Information leaflet Patient Information leaflet Danish 04-08-2021
Public Assessment Report Public Assessment Report Danish 04-08-2021
Patient Information leaflet Patient Information leaflet German 04-08-2021
Public Assessment Report Public Assessment Report German 04-08-2021
Patient Information leaflet Patient Information leaflet Estonian 04-08-2021
Public Assessment Report Public Assessment Report Estonian 04-08-2021
Patient Information leaflet Patient Information leaflet Greek 04-08-2021
Public Assessment Report Public Assessment Report Greek 04-08-2021
Patient Information leaflet Patient Information leaflet English 04-08-2021
Public Assessment Report Public Assessment Report English 04-08-2021
Patient Information leaflet Patient Information leaflet French 04-08-2021
Public Assessment Report Public Assessment Report French 04-08-2021
Patient Information leaflet Patient Information leaflet Italian 04-08-2021
Public Assessment Report Public Assessment Report Italian 04-08-2021
Patient Information leaflet Patient Information leaflet Latvian 04-08-2021
Public Assessment Report Public Assessment Report Latvian 04-08-2021
Patient Information leaflet Patient Information leaflet Lithuanian 04-08-2021
Summary of Product characteristics Summary of Product characteristics Lithuanian 04-08-2021
Public Assessment Report Public Assessment Report Lithuanian 04-08-2021
Patient Information leaflet Patient Information leaflet Hungarian 04-08-2021
Summary of Product characteristics Summary of Product characteristics Hungarian 04-08-2021
Public Assessment Report Public Assessment Report Hungarian 04-08-2021
Patient Information leaflet Patient Information leaflet Maltese 04-08-2021
Public Assessment Report Public Assessment Report Maltese 04-08-2021
Patient Information leaflet Patient Information leaflet Dutch 04-08-2021
Public Assessment Report Public Assessment Report Dutch 04-08-2021
Patient Information leaflet Patient Information leaflet Polish 04-08-2021
Public Assessment Report Public Assessment Report Polish 04-08-2021
Patient Information leaflet Patient Information leaflet Portuguese 04-08-2021
Summary of Product characteristics Summary of Product characteristics Portuguese 04-08-2021
Public Assessment Report Public Assessment Report Portuguese 04-08-2021
Patient Information leaflet Patient Information leaflet Romanian 04-08-2021
Public Assessment Report Public Assessment Report Romanian 04-08-2021
Patient Information leaflet Patient Information leaflet Slovak 04-08-2021
Public Assessment Report Public Assessment Report Slovak 04-08-2021
Patient Information leaflet Patient Information leaflet Slovenian 04-08-2021
Summary of Product characteristics Summary of Product characteristics Slovenian 04-08-2021
Public Assessment Report Public Assessment Report Slovenian 04-08-2021
Patient Information leaflet Patient Information leaflet Finnish 04-08-2021
Public Assessment Report Public Assessment Report Finnish 04-08-2021
Patient Information leaflet Patient Information leaflet Swedish 04-08-2021
Public Assessment Report Public Assessment Report Swedish 04-08-2021
Patient Information leaflet Patient Information leaflet Norwegian 04-08-2021
Summary of Product characteristics Summary of Product characteristics Norwegian 04-08-2021
Patient Information leaflet Patient Information leaflet Icelandic 04-08-2021
Summary of Product characteristics Summary of Product characteristics Icelandic 04-08-2021
Patient Information leaflet Patient Information leaflet Croatian 04-08-2021
Public Assessment Report Public Assessment Report Croatian 04-08-2021

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