Pemetrexed Pfizer (previously Pemetrexed Hospira)

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

pemetrexed disodium, pemetrexed disodium hemipentahydrate

Available from:

Pfizer Europe MA EEIG

ATC code:

L01BA04

INN (International Name):

pemetrexed

Therapeutic group:

Антинеопластични средства

Therapeutic area:

Carcinoma, Non-Small-Cell Lung; Mesothelioma

Therapeutic indications:

Malignant pleural mesotheliomaPemetrexed Pfizer in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. Non-small cell lung cancerPemetrexed Pfizer in combination with cisplatin is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology. Pemetrexed Pfizer is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy. Pemetrexed Pfizer is indicated as monotherapy for the second-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.

Product summary:

Revision: 14

Authorization status:

упълномощен

Authorization date:

2015-11-19

Patient Information leaflet

                                63
Б. ЛИСТОВКА
64
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
ПЕМЕТРЕКСЕД PFIZER 100 MG ПРАХ ЗА
КОНЦЕНТРАТ ЗА ИНФУЗИОНЕН РАЗТВОР
ПЕМЕТРЕКСЕД PFIZER 500 MG ПРАХ ЗА
КОНЦЕНТРАТ ЗА ИНФУЗИОНЕН РАЗТВОР
ПЕМЕТРЕКСЕД PFIZER 1 000 MG ПРАХ ЗА
КОНЦЕНТРАТ ЗА ИНФУЗИОНЕН РАЗТВОР
пеметрексед (pemetrexed)
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,
фармацевт или
медицинска сестра.
-
Ако получите някакви нежелани
лекарствени 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 Пеметрексед Pfizer и
за какво се използва
2.
Какво трябва да знаете, преди да
използвате Пеметрексед Pfizer
3.
Как да използвате Пеметрексед Pfizer
4.
Възможни нежелани реакции
5.
Как да съхранявате Пеметрексед Pfizer
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА ПЕМЕТРЕКСЕД PFIZER И
ЗА КАКВО СЕ ИЗПОЛЗВА
Пем
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Пеметрексед Pfizer 100 mg прах за
концентрат за инфузионен разтвор
Пеметрексед Pfizer 500 mg прах за
концентрат за инфузионен разтвор
Пеметрексед Pfizer 1 000 mg прах за
концентрат за инфузионен разтвор
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Пеметрексед Pfizer 100 mg прах за
концентрат за инфузионен разтвор
Всеки флакон съдържа 100 mg пеметрексед
(_pemetrexed_) (като пеметрексед динатрий
хемипентахидрат).
_Помощно вещество с известно действие_
Всеки флакон съдържа приблизително 11
mg натрий.
Пеметрексед Pfizer 500 mg прах за
концентрат за инфузионен разтвор
Всеки флакон съдържа 500 mg пеметрексед
(_pemetrexed_) (като пеметрексед динатрий
хемипентахидрат).
_Помощно вещество с известно действие_
Всеки флакон съдържа приблизително 54
mg натрий.
Пеметрексед Pfizer 1 000 mg прах за
концентрат за инфузионен разтвор
Всеки флакон съдържа 1 000 mg пеметрексед
(_pemetrexed_) (като пеметрексед динатрий
хемипентахидрат).
_Помощно вещество с известно действие_
Всеки флакон съдържа приблизително 108
mg натрий.
След разтваряне (реконституиране) (вж.
точка 6.6), всеки флакон съдържа 25 mg/ml
пеметрексед.
За пълния спи
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 21-09-2022
Public Assessment Report Public Assessment Report Spanish 01-12-2015
Patient Information leaflet Patient Information leaflet Czech 21-09-2022
Public Assessment Report Public Assessment Report Czech 01-12-2015
Patient Information leaflet Patient Information leaflet Danish 21-09-2022
Public Assessment Report Public Assessment Report Danish 01-12-2015
Patient Information leaflet Patient Information leaflet German 21-09-2022
Public Assessment Report Public Assessment Report German 01-12-2015
Patient Information leaflet Patient Information leaflet Estonian 21-09-2022
Public Assessment Report Public Assessment Report Estonian 01-12-2015
Patient Information leaflet Patient Information leaflet Greek 21-09-2022
Public Assessment Report Public Assessment Report Greek 01-12-2015
Patient Information leaflet Patient Information leaflet English 21-09-2022
Public Assessment Report Public Assessment Report English 01-12-2015
Patient Information leaflet Patient Information leaflet French 21-09-2022
Public Assessment Report Public Assessment Report French 01-12-2015
Patient Information leaflet Patient Information leaflet Italian 21-09-2022
Public Assessment Report Public Assessment Report Italian 01-12-2015
Patient Information leaflet Patient Information leaflet Latvian 21-09-2022
Public Assessment Report Public Assessment Report Latvian 01-12-2015
Patient Information leaflet Patient Information leaflet Lithuanian 21-09-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 21-09-2022
Public Assessment Report Public Assessment Report Lithuanian 01-12-2015
Patient Information leaflet Patient Information leaflet Hungarian 21-09-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 21-09-2022
Public Assessment Report Public Assessment Report Hungarian 01-12-2015
Patient Information leaflet Patient Information leaflet Maltese 21-09-2022
Public Assessment Report Public Assessment Report Maltese 01-12-2015
Patient Information leaflet Patient Information leaflet Dutch 21-09-2022
Public Assessment Report Public Assessment Report Dutch 01-12-2015
Patient Information leaflet Patient Information leaflet Polish 21-09-2022
Public Assessment Report Public Assessment Report Polish 01-12-2015
Patient Information leaflet Patient Information leaflet Portuguese 21-09-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 21-09-2022
Public Assessment Report Public Assessment Report Portuguese 01-12-2015
Patient Information leaflet Patient Information leaflet Romanian 21-09-2022
Public Assessment Report Public Assessment Report Romanian 01-12-2015
Patient Information leaflet Patient Information leaflet Slovak 21-09-2022
Public Assessment Report Public Assessment Report Slovak 01-12-2015
Patient Information leaflet Patient Information leaflet Slovenian 21-09-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 21-09-2022
Public Assessment Report Public Assessment Report Slovenian 01-12-2015
Patient Information leaflet Patient Information leaflet Finnish 21-09-2022
Public Assessment Report Public Assessment Report Finnish 01-12-2015
Patient Information leaflet Patient Information leaflet Swedish 21-09-2022
Public Assessment Report Public Assessment Report Swedish 01-12-2015
Patient Information leaflet Patient Information leaflet Norwegian 21-09-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 21-09-2022
Patient Information leaflet Patient Information leaflet Icelandic 21-09-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 21-09-2022
Patient Information leaflet Patient Information leaflet Croatian 21-09-2022
Public Assessment Report Public Assessment Report Croatian 01-12-2015

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