Arsenic trioxide medac

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

Арсеник Триоксид

Available from:

medac Gesellschaft für klinische Spezialpräparate mbH

ATC code:

L01XX27

INN (International Name):

arsenic trioxide

Therapeutic group:

Антинеопластични средства

Therapeutic area:

Левкемия, промиелоцитна, остра

Therapeutic indications:

Arsenic trioxide medac is indicated for induction of remission, and consolidation in adult patients with:Newly diagnosed low-to-intermediate risk acute promyelocytic leukaemia (APL) (white blood cell count, ≤ 10 x 10³/μl) in combination with all-trans-retinoic acid (ATRA)Relapsed/refractory APL (previous treatment should have included a retinoid and chemotherapy) characterised by the presence of the t(15;17) translocation and/or the presence of the pro-myelocytic leukaemia/retinoic-acid-receptor-alpha (PML/RARα) gene. Скоростта на реакция друг остър миелобластный подтипове на левкемия до триоксида арсен не е считан за.

Product summary:

Revision: 2

Authorization status:

упълномощен

Authorization date:

2020-09-17

Patient Information leaflet

                                27
Б. ЛИСТОВКА
28
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
АРСЕНОВ ТРИОКСИД MEDAC 1 MG/ML КОНЦЕНТРАТ
ЗА ИНФУЗИОНЕН РАЗТВОР
arsenic trioxide (арсенов триоксид)
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ВИ СЕ ДАДЕ 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 Арсенов триоксид
medac и за какво се използва
2.
Какво трябва да знаете, преди да Ви се
даде Арсенов триоксид medac
3.
Как се използва Арсенов триоксид medac
4.
Възможни нежелани реакции
5
Как да съхранявате Арсенов триоксид
medac
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА АРСЕНОВ ТРИОКСИД
MEDAC И ЗА КАКВО СЕ ИЗПОЛЗВА
Арсенов триоксид medac съдържа
активното вещество арсенов триоксид,
което е лекарство
против рак. Механизмът на действие на
Арсено
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Арсенов триоксид medac 1 mg/ml концентрат
за инфузионен разтвор
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Всеки ml от концентрата съдържа 1 mg
арсенов триоксид (arsenic trioxide).
Един флакон от 10 ml съдържа 10 mg арсенов
триоксид (arsenic trioxide).
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Концентрат за инфузионен разтвор
(стерилен концентрат).
Стерилен, бистър, безцветен, воден
разтвор, без видими частици. pH на
разтвора е 6,0-8,0.
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Арсенов триоксид medac е показан за
индукция на ремисия и консолидация
при възрастни
пациенти с:
•
новодиагностицирана, ниско до средно
рискова, остра промиелоцитна левкемия
(ОПЛ)
(брой на белите кръвни клетки ≤10 x
10³/µl) в комбинация с
_транс_
-ретиноева киселина
(all-
_trans_
-retinoic acid, ATRA),
•
рецидивираща/рефрактерна ОПЛ
(предходното лечение трябва да е
включвало ретиноид
и химиотерапия),
характеризираща се с наличието на t
(15;17) транслокация и/или наличието на
ген за
промиелоцитна левкемия/алфа рецептор
на ретиноевата киселина (pro-myelocytic
leukaemia/retinoic-acid-receptor-alpha, PML/RARα).
Степента н
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 26-04-2022
Public Assessment Report Public Assessment Report Spanish 01-10-2020
Patient Information leaflet Patient Information leaflet Czech 26-04-2022
Public Assessment Report Public Assessment Report Czech 01-10-2020
Patient Information leaflet Patient Information leaflet Danish 26-04-2022
Public Assessment Report Public Assessment Report Danish 01-10-2020
Patient Information leaflet Patient Information leaflet German 26-04-2022
Public Assessment Report Public Assessment Report German 01-10-2020
Patient Information leaflet Patient Information leaflet Estonian 26-04-2022
Public Assessment Report Public Assessment Report Estonian 01-10-2020
Patient Information leaflet Patient Information leaflet Greek 26-04-2022
Public Assessment Report Public Assessment Report Greek 01-10-2020
Patient Information leaflet Patient Information leaflet English 26-04-2022
Public Assessment Report Public Assessment Report English 01-10-2020
Patient Information leaflet Patient Information leaflet French 26-04-2022
Public Assessment Report Public Assessment Report French 01-10-2020
Patient Information leaflet Patient Information leaflet Italian 26-04-2022
Public Assessment Report Public Assessment Report Italian 01-10-2020
Patient Information leaflet Patient Information leaflet Latvian 26-04-2022
Public Assessment Report Public Assessment Report Latvian 01-10-2020
Patient Information leaflet Patient Information leaflet Lithuanian 26-04-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 26-04-2022
Public Assessment Report Public Assessment Report Lithuanian 01-10-2020
Patient Information leaflet Patient Information leaflet Hungarian 26-04-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 26-04-2022
Public Assessment Report Public Assessment Report Hungarian 01-10-2020
Patient Information leaflet Patient Information leaflet Maltese 26-04-2022
Public Assessment Report Public Assessment Report Maltese 01-10-2020
Patient Information leaflet Patient Information leaflet Dutch 26-04-2022
Public Assessment Report Public Assessment Report Dutch 01-10-2020
Patient Information leaflet Patient Information leaflet Polish 26-04-2022
Public Assessment Report Public Assessment Report Polish 01-10-2020
Patient Information leaflet Patient Information leaflet Portuguese 26-04-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 26-04-2022
Public Assessment Report Public Assessment Report Portuguese 01-10-2020
Patient Information leaflet Patient Information leaflet Romanian 26-04-2022
Public Assessment Report Public Assessment Report Romanian 01-10-2020
Patient Information leaflet Patient Information leaflet Slovak 26-04-2022
Public Assessment Report Public Assessment Report Slovak 01-10-2020
Patient Information leaflet Patient Information leaflet Slovenian 26-04-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 26-04-2022
Public Assessment Report Public Assessment Report Slovenian 01-10-2020
Patient Information leaflet Patient Information leaflet Finnish 26-04-2022
Public Assessment Report Public Assessment Report Finnish 01-10-2020
Patient Information leaflet Patient Information leaflet Swedish 26-04-2022
Public Assessment Report Public Assessment Report Swedish 01-10-2020
Patient Information leaflet Patient Information leaflet Norwegian 26-04-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 26-04-2022
Patient Information leaflet Patient Information leaflet Icelandic 26-04-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 26-04-2022
Patient Information leaflet Patient Information leaflet Croatian 26-04-2022
Public Assessment Report Public Assessment Report Croatian 01-10-2020