Mircera

Country: European Union

Language: Italian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

Metossi polietilene glicole-epoetina beta

Available from:

Roche Registration GmbH

ATC code:

B03XA03

INN (International Name):

methoxy polyethylene glycol-epoetin beta

Therapeutic group:

Preparazioni antianemiche

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:

autorizzato

Authorization date:

2007-07-20

Patient Information leaflet

                                54
B. FOGLIO ILLUSTRATIVO
55
FOGLIO ILLUSTRATIVO: INFORMAZIONI PER L’UTILIZZATORE
MIRCERA
30 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
40 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
50 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
60 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
75 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
100 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
120 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
150 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
200 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
250 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
360 MICROGRAMMI/0,6 ML SOLUZIONE INIETTABILE IN SIRINGA PRERIEMPITA
metossipolietilenglicole-epoetina
beta
LEGGA ATTENTAMENTE QUESTO FOGLIO PRIMA DI USARE QUESTO MEDICINALE
PERCHÈ CONTIENE IMPORTANTI
INFORMAZIONI PER LEI.
•
Conservi questo foglio. Potrebbe aver bisogno di leggerlo di nuovo.
•
Se ha qualsiasi dubbio, si rivolga al medico o al farmacista.
•
Questo medicinale è stato prescritto soltanto per lei. Non lo dia ad
altre persone, anche se i
sintomi della malattia sono uguali ai suoi, perché potrebbe essere
pericoloso.
•
Se si manifesta un qualsiasi effetto indesiderato, compresi quelli non
elencati in questo foglio, si
rivolga al medico. Vedere paragrafo 4.
CONTENUTO DI QUESTO FOGLIO
:
1.
Cos’è MIRCERA e a cosa serve
2.
Cosa deve sapere prima di usare MIRCERA
3.
Come usare MIRCERA
4.
Possibili effetti indesiderati
5.
Come conservare MIRCERA
6.
Contenuto della confezione e altre informazioni
1.
COS' È MIRCERA E A COSA SERVE
Questo medicinale le è stato prescritto perché soffre di anemia
causata da malattia renale cronica e
associata a sintomi tipici quali stanchezza, debolezza e affanno.
Questo significa che il sangue
contiene una quantità insufficiente di globuli rossi e il livello
dell'emoglobina è troppo basso (i tessuti
del corpo p
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ALLEGATO I
RIASSUNTO DELLE CARATTERISTICHE DEL PRODOTTO
2
1.
DENOMINAZIONE DEL MEDICINALE
MIRCERA 30 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 40 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 50 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 60 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 75 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 100 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 120 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 150 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 200 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 250 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
MIRCERA 360 MICROGRAMMI/0,6 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
2.
COMPOSIZIONE QUALITATIVA E QUANTITATIVA
MIRCERA 30 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
Una siringa preriempita contiene 30 microgrammi di
metossipolietilenglicole-epoetina beta*, ad una
concentrazione di 100 microgrammi/mL.
MIRCERA 40 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
Una siringa preriempita contiene 40 microgrammi di
metossipolietilenglicole-epoetina beta*, ad una
concentrazione di 133 microgrammi/mL.
MIRCERA 50 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
Una siringa preriempita contiene 50 microgrammi di
metossipolietilenglicole-epoetina beta*, ad una
concentrazione di 167 microgrammi/mL.
MIRCERA 60 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
Una siringa preriempita contiene 60 microgrammi di
metossipolietilenglicole-epoetina beta*, ad una
concentrazione di 200 microgrammi/mL.
MIRCERA 75 MICROGRAMMI/0,3 ML SOLUZIONE INIETTABILE IN SIRINGA
PRERIEMPITA
Una siringa preriempita contiene 75 microgrammi di
metossipolietilenglicole-epoetina beta*, ad una
concentrazione di 250 microgrammi/mL.
MIRCERA 100 MICROGRAMM
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 07-12-2023
Public Assessment Report Public Assessment Report Bulgarian 11-08-2023
Patient Information leaflet Patient Information leaflet Spanish 07-12-2023
Public Assessment Report Public Assessment Report Spanish 11-08-2023
Patient Information leaflet Patient Information leaflet Czech 07-12-2023
Public Assessment Report Public Assessment Report Czech 11-08-2023
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
Public Assessment Report Public Assessment Report French 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
Public Assessment Report Public Assessment Report Dutch 11-08-2023
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

View documents history