Mircera

Country: European Union

Language: Icelandic

Source: EMA (European Medicines Agency)

Active ingredient:

Metoxý annara hættu efst-epóetín beta

Available from:

Roche Registration GmbH

ATC code:

B03XA03

INN (International Name):

methoxy polyethylene glycol-epoetin beta

Therapeutic group:

Sýklalyf

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:

Leyfilegt

Authorization date:

2007-07-20

Patient Information leaflet

                                53
B. FYLGISEÐILL
54
FYLGISEÐILL: UPPLÝSINGAR FYRIR NOTANDA LYFSINS
MIRCERA
30 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
40 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
50 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
60 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
75 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
100 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
120 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
150 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
200 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
250 MÍKRÓGRÖMM/0,3 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
360 MÍKRÓGRÖMM/0,6 ML AF STUNGULYFI, LAUSN Í ÁFYLLTRI SPRAUTU
metoxýpólýetýlen glýkól-epóetín beta
LESIÐ ALLAN FYLGISEÐILINN VANDLEGA ÁÐUR EN BYRJAÐ ER AÐ NOTA
LYFIÐ. Í HONUM ERU MIKILVÆGAR
UPPLÝSINGAR.
•
Geymið fylgiseðilinn. Nauðsynlegt getur verið að lesa hann
síðar.
•
Leitið til læknisins eða lyfjafræðings ef þörf er á frekari
upplýsingum.
•
Þessu lyfi hefur verið ávísað til persónulegra nota. Ekki má
gefa það öðrum. Það getur valdið
þeim skaða, jafnvel þótt um sömu sjúkdómseinkenni sé að
ræða.
•
Látið lækninn vita um allar aukaverkanir. Þetta gildir einnig um
aukaverkanir sem ekki er
minnst á í þessum fylgiseðli. Sjá kafla 4.
Í FYLGISEÐLINUM ERU EFTIRFARANDI KAFLAR
:
1.
Upplýsingar um MIRCERA og við hverju það er notað
2.
Áður en byrjað er að nota MIRCERA
3.
Hvernig nota á MIRCERA
4.
Hugsanlegar aukaverkanir
5.
Hvernig geyma á MIRCERA
6.
Pakkningar og aðrar upplýsingar
1.
UPPLÝSINGAR UM MIRCERA OG VIÐ HVERJU ÞAÐ ER NOTAÐ
Þessu lyfi hefur verið ávísað vegna blóðleysis sem er af
völdum langvinns nýrnasjúkdóms og tengist
dæmigerðum einkennum eins og þreytu, þróttleysi og mæði. Það
þýðir að of lítið er af rauðum
blóðkornum í blóðinu og blóðrauðagild
                                
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Summary of Product characteristics

                                1
VIÐAUKI I
SAMANTEKT Á EIGINLEIKUM LYFS
2
1.
HEITI LYFS
MIRCERA 30 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 40 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 50 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 60 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 75 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 100 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 120 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 150 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 200 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 250 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
MIRCERA 360 MÍKRÓGRÖMM/0,6 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
2.
INNIHALDSLÝSING
MIRCERA 30 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
Ein áfyllt sprauta inniheldur 30 míkrógrömm af
metoxýpólýetýlen glýkól-epóetín beta* í
styrkleikanum 100 míkrógrömm/ml.
MIRCERA 40 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
Ein áfyllt sprauta inniheldur 40 míkrógrömm af
metoxýpólýetýlen glýkól-epóetín beta* í
styrkleikanum 133 míkrógrömm/ml.
MIRCERA 50 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
Ein áfyllt sprauta inniheldur 50 míkrógrömm af
metoxýpólýetýlen glýkól-epóetín beta* í
styrkleikanum 167 míkrógrömm/ml.
MIRCERA 60 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
Ein áfyllt sprauta inniheldur 60 míkrógrömm af
metoxýpólýetýlen glýkól-epóetín beta* í
styrkleikanum 200 míkrógrömm/ml.
MIRCERA 75 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
Ein áfyllt sprauta inniheldur 75 míkrógrömm af
metoxýpólýetýlen glýkól-epóetín beta* í
styrkleikanum 250 míkrógrömm/ml.
MIRCERA 100 MÍKRÓGRÖMM/0,3 ML STUNGULYF, LAUSN Í ÁFYLLTRI SPRAUTU
Ein áfyllt sprauta inniheldur 100 míkrógrömm af
metoxýpólýetýlen glýkól-epóetín 
                                
                                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 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
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 Croatian 07-12-2023
Public Assessment Report Public Assessment Report Croatian 11-08-2023

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