Zydelig

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

Idelalisib

Available from:

Gilead Sciences Ireland UC

ATC code:

L01XX47

INN (International Name):

idelalisib

Therapeutic group:

Antineoplastic agents, Other antineoplastic agents

Therapeutic area:

Lymphoma, Non-Hodgkin; Leukemia, Lymphocytic, Chronic, B-Cell

Therapeutic indications:

Zydelig is indicated in combination with an anti‑CD20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (CLL):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or TP53 mutation in patients who are not eligible for any other therapies. Zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (FL) that is refractory to two prior lines of treatment.

Product summary:

Revision: 20

Authorization status:

упълномощен

Authorization date:

2014-09-18

Patient Information leaflet

                                59
Б. ЛИСТОВКА
60
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПАЦИЕНТА
ZYDELIG 100 MG ФИЛМИРАНИ ТАБЛЕТКИ
иделалисиб (idelalisib)
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ЗАПОЧНЕТЕ ДА ПРИЕМАТЕ ТОВА
ЛЕКАРСТВО,
ТЪЙ КАТО ТЯ СЪДЪРЖА ВАЖНА ЗА ВАС
ИНФОРМАЦИЯ.
-
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въпроси, попитайте Вашия лекар.
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Вас. Не го преотстъпвайте на други
хора. То може
да им навреди, независимо че
признаците на тяхното заболяване са
същите като Вашите.
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реакции, уведомете Вашия лекар. Това
включва и
всички възможни нежелани реакции,
неописани в тази листовка. Вижте точка
4.
КАКВО СЪДЪРЖА ТАЗИ ЛИСТОВКА
1.
Какво представлява Zydelig и за какво се
използва
2.
Какво трябва да знаете, преди да
приемете Zydelig
3.
Как да приемате Zydelig
4.
Възможни нежелани реакции
5.
Как да съхранявате Zydelig
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА ZYDELIG И ЗА КАКВО СЕ
ИЗПОЛЗВА
Zydelig е противораково лекарство, което
съдържа активното вещество
иделалисиб. То действа
като блокира действието на един ензим,
който участв
                                
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Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Zydelig 100 mg филмирани таблетки
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Всяка филмирана таблетка съдържа 100 mg
иделалисиб (idelalisib).
Помощно(и) вещество(а) с известно
действие
Всяка таблетка съдържа 0,1 mg сънсет
жълто FCF (E110) (вж. точка 4.4).
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Филмирана таблетка
Оранжева филмирана таблетка с овална
форма, с размери 9,7 mm на 6,0 mm, с
вдлъбнато
релефно означение “GSI” от едната
страна и “100” от другата страна.
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Zydelig е показан в комбинация с
ритуксимаб за лечение на възрастни
пациенти с хронична
лимфоцитна левкемия (ХЛЛ):
•
които са били подложени на поне една
предходна терапия (вж. точка 4.4), или
•
като лечение от първа линия при
наличие на делеция 17p или
_TP53 _
мутация при
пациенти, които не са подходящи за
други терапии (вж. точка 4.4).
Zydelig е показан като монотерапия за
лечение на възрастни пациенти с
фоликуларен лимфом
(ФЛ), рефрактерен към две предишни
линии на лечение (вж. точка 4.4).
4.2
ДОЗИРОВКА И НАЧИН НА ПРИЛОЖЕНИЕ
Лечението със Zydelig трябва да се

                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 23-06-2023
Public Assessment Report Public Assessment Report Spanish 10-01-2020
Patient Information leaflet Patient Information leaflet Czech 23-06-2023
Public Assessment Report Public Assessment Report Czech 10-01-2020
Patient Information leaflet Patient Information leaflet Danish 23-06-2023
Public Assessment Report Public Assessment Report Danish 10-01-2020
Patient Information leaflet Patient Information leaflet German 23-06-2023
Public Assessment Report Public Assessment Report German 10-01-2020
Patient Information leaflet Patient Information leaflet Estonian 23-06-2023
Public Assessment Report Public Assessment Report Estonian 10-01-2020
Patient Information leaflet Patient Information leaflet Greek 23-06-2023
Public Assessment Report Public Assessment Report Greek 10-01-2020
Patient Information leaflet Patient Information leaflet English 23-06-2023
Public Assessment Report Public Assessment Report English 10-01-2020
Patient Information leaflet Patient Information leaflet French 23-06-2023
Public Assessment Report Public Assessment Report French 10-01-2020
Patient Information leaflet Patient Information leaflet Italian 23-06-2023
Public Assessment Report Public Assessment Report Italian 10-01-2020
Patient Information leaflet Patient Information leaflet Latvian 23-06-2023
Public Assessment Report Public Assessment Report Latvian 10-01-2020
Patient Information leaflet Patient Information leaflet Lithuanian 23-06-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 23-06-2023
Public Assessment Report Public Assessment Report Lithuanian 10-01-2020
Patient Information leaflet Patient Information leaflet Hungarian 23-06-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 23-06-2023
Public Assessment Report Public Assessment Report Hungarian 10-01-2020
Patient Information leaflet Patient Information leaflet Maltese 23-06-2023
Public Assessment Report Public Assessment Report Maltese 10-01-2020
Patient Information leaflet Patient Information leaflet Dutch 23-06-2023
Public Assessment Report Public Assessment Report Dutch 10-01-2020
Patient Information leaflet Patient Information leaflet Polish 23-06-2023
Public Assessment Report Public Assessment Report Polish 10-01-2020
Patient Information leaflet Patient Information leaflet Portuguese 23-06-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 23-06-2023
Public Assessment Report Public Assessment Report Portuguese 10-01-2020
Patient Information leaflet Patient Information leaflet Romanian 23-06-2023
Public Assessment Report Public Assessment Report Romanian 10-01-2020
Patient Information leaflet Patient Information leaflet Slovak 23-06-2023
Public Assessment Report Public Assessment Report Slovak 10-01-2020
Patient Information leaflet Patient Information leaflet Slovenian 23-06-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 23-06-2023
Public Assessment Report Public Assessment Report Slovenian 10-01-2020
Patient Information leaflet Patient Information leaflet Finnish 23-06-2023
Public Assessment Report Public Assessment Report Finnish 10-01-2020
Patient Information leaflet Patient Information leaflet Swedish 23-06-2023
Public Assessment Report Public Assessment Report Swedish 10-01-2020
Patient Information leaflet Patient Information leaflet Norwegian 23-06-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 23-06-2023
Patient Information leaflet Patient Information leaflet Icelandic 23-06-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 23-06-2023
Patient Information leaflet Patient Information leaflet Croatian 23-06-2023
Public Assessment Report Public Assessment Report Croatian 10-01-2020

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