Mircera

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

Метокси полиетилен гликол-эпоэтин бета

Available from:

Roche Registration GmbH

ATC code:

B03XA03

INN (International Name):

methoxy polyethylene glycol-epoetin beta

Therapeutic group:

Антианемични препарати

Therapeutic area:

Anemia; Kidney Failure, Chronic

Therapeutic indications:

Treatment of symptomatic anaemia associated with chronic kidney disease (CKD) in adult patients (see section 5. Treatment of symptomatic anaemia associated with chronic kidney disease (CKD) in paediatric patients from 3 months to less than 18 years of age who are converting from another erythropoiesis stimulating agent (ESA) after their haemoglobin level was stabilised with the previous ESA (see section 5.

Product summary:

Revision: 29

Authorization status:

упълномощен

Authorization date:

2007-07-20

Patient Information leaflet

                                58
Б. ЛИСТОВКА
59
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
MIRCERA
30 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
40 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
50 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
60 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
75 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
100 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
120 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
150 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
200 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
250 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
360 МИКРОГРАМА/0,6 ML ИНЖЕКЦИОНЕН РАЗТВОР
В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА СПРИНЦОВКА
метоксиполиетилен гликол – епоетин
бета (methoxy polyethylene glycol-epoetin beta)
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ЗАПОЧНЕТЕ ДА ИЗПОЛЗВАТЕ ТОВА
ЛЕКАРСТВО, ТЪЙ КАТО ТЯ СЪДЪРЖА ВАЖНА
ЗА ВАС ИНФОРМАЦИЯ.
•
Запазете тази листовка. М
                                
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Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
MIRCERA 30 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 40 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 50 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 60 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 75 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 100 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 120 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 150 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 200 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 250 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
MIRCERA 360 МИКРОГРАМА/0,6 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
MIRCERA 30 МИКРОГРАМА/0,3 ML ИНЖЕКЦИОНЕН
РАЗТВОР В ПРЕДВАРИТЕЛНО НАПЪЛНЕНА
СПРИНЦОВКА
Една предварително напълнена
спринцов
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 07-12-2023
Public Assessment Report Public Assessment Report Spanish 11-08-2023
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Patient Information leaflet Patient Information leaflet Danish 07-12-2023
Public Assessment Report Public Assessment Report Danish 11-08-2023
Patient Information leaflet Patient Information leaflet German 07-12-2023
Public Assessment Report Public Assessment Report German 11-08-2023
Patient Information leaflet Patient Information leaflet Estonian 07-12-2023
Public Assessment Report Public Assessment Report Estonian 11-08-2023
Patient Information leaflet Patient Information leaflet Greek 07-12-2023
Public Assessment Report Public Assessment Report Greek 11-08-2023
Patient Information leaflet Patient Information leaflet English 07-12-2023
Public Assessment Report Public Assessment Report English 11-08-2023
Patient Information leaflet Patient Information leaflet French 07-12-2023
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Patient Information leaflet Patient Information leaflet Italian 07-12-2023
Public Assessment Report Public Assessment Report Italian 11-08-2023
Patient Information leaflet Patient Information leaflet Latvian 07-12-2023
Public Assessment Report Public Assessment Report Latvian 11-08-2023
Patient Information leaflet Patient Information leaflet Lithuanian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 07-12-2023
Public Assessment Report Public Assessment Report Lithuanian 11-08-2023
Patient Information leaflet Patient Information leaflet Hungarian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 07-12-2023
Public Assessment Report Public Assessment Report Hungarian 11-08-2023
Patient Information leaflet Patient Information leaflet Maltese 07-12-2023
Public Assessment Report Public Assessment Report Maltese 11-08-2023
Patient Information leaflet Patient Information leaflet Dutch 07-12-2023
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Patient Information leaflet Patient Information leaflet Polish 07-12-2023
Public Assessment Report Public Assessment Report Polish 11-08-2023
Patient Information leaflet Patient Information leaflet Portuguese 07-12-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 07-12-2023
Public Assessment Report Public Assessment Report Portuguese 11-08-2023
Patient Information leaflet Patient Information leaflet Romanian 07-12-2023
Public Assessment Report Public Assessment Report Romanian 11-08-2023
Patient Information leaflet Patient Information leaflet Slovak 07-12-2023
Public Assessment Report Public Assessment Report Slovak 11-08-2023
Patient Information leaflet Patient Information leaflet Slovenian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 07-12-2023
Public Assessment Report Public Assessment Report Slovenian 11-08-2023
Patient Information leaflet Patient Information leaflet Finnish 07-12-2023
Public Assessment Report Public Assessment Report Finnish 11-08-2023
Patient Information leaflet Patient Information leaflet Swedish 07-12-2023
Public Assessment Report Public Assessment Report Swedish 11-08-2023
Patient Information leaflet Patient Information leaflet Norwegian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 07-12-2023
Patient Information leaflet Patient Information leaflet Icelandic 07-12-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 07-12-2023
Patient Information leaflet Patient Information leaflet Croatian 07-12-2023
Public Assessment Report Public Assessment Report Croatian 11-08-2023

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