Voncento

Country: European Union

Language: Icelandic

Source: EMA (European Medicines Agency)

Active ingredient:

Mönnum storknun þáttur VIII, mönnum von willebrand þáttur

Available from:

CSL Behring GmbH

ATC code:

B02BD06

INN (International Name):

human coagulation factor VIII / human von willebrand factor

Therapeutic group:

Blood coagulation factors, von Willebrand factor and coagulation factor VIII in combination, Antihemorrhagics

Therapeutic area:

Hemophilia A; von Willebrand Diseases

Therapeutic indications:

Von Willebrand sjúkdómur (VWD)Fyrirbyggja og meðferð blæðing eða skurðaðgerð blæðingar í sjúklinga með VWD, þegar desmópressín (DDAVP) meðferð einn er ófullnægjandi eða handa. Dreyrasýki (meðfædda þáttur-VIII skort)Fyrirbyggja og meðferð blæðingar í sjúklinga með dreyrasýki A.

Product summary:

Revision: 15

Authorization status:

Leyfilegt

Authorization date:

2013-08-12

Patient Information leaflet

                                41
B. FYLGISEÐILL
42
FYLGISEÐILL: UPPLÝSINGAR FYRIR NOTANDA LYFSINS
VONCENTO 250 A.E. FVIII / 600 A.E. VWF (5 ML LEYSIR)
STUNGULYFS-/INNRENNSLISSTOFN OG LEYSIR, LAUSN
VONCENTO 500 A.E. FVIII / 1200 A.E. VWF (10 ML LEYSIR)
STUNGULYFS-/INNRENNSLISSTOFN OG LEYSIR,
LAUSN
VONCENTO 500 A.E. FVIII / 1200 A.E. VWF (5 ML LEYSIR)
STUNGULYFS-/INNRENNSLISSTOFN OG LEYSIR,
LAUSN
VONCENTO 1000 A.E. FVIII / 2400 A.E. VWF (10 ML LEYSIR)
STUNGULYFS-/INNRENNSLISSTOFN OG LEYSIR,
LAUSN
manna storkuþáttur VIII
manna von Willebrand þáttur,
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, lyfjafræðings eða hjúkrunarfræðingsins
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, lyfjafræðing eða hjúkrunarfræðinginn 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 Voncento og við hverju það er notað
2.
Áður en byrjað er að nota Voncento
3.
Hvernig nota á Voncento
4.
Hugsanlegar aukaverkanir
5.
Hvernig geyma á Voncento
6.
Pakkningar og aðrar upplýsingar
1.
UPPLÝSINGAR UM VONCENTO OG VIÐ HVERJU ÞAÐ ER NOTAÐ
Lyfið er búið til úr blóðvökva manna og inniheldur virk efni
sem nefnast manna storkuþáttur VIII
(FVIII) og manna von Willebrand þáttur (VWF).
Voncento er notað til að fyrirbyggja eða stöðva blæðingar af
völdum skorts á VWF í von Willebrand
sjúkdómi (VWD) eða skorts á FVIII í dreyrasýki A hjá
sjúklingum á öllum aldri. Voncento er aðeins
notað ef meðferð með öðru lyfi, desmópressíni, dugar ekki ein
sér eða ef ekki er hægt að beita henni.
VWF og FVIII taka þátt í blóðstork
                                
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Summary of Product characteristics

                                1
VIÐAUKI I
SAMANTEKT Á EIGINLEIKUM LYFS
2
1.
HEITI LYFS
Voncento 250 a.e. FVIII / 600 a.e. VWF (5 ml leysir)
stungulyfs-/innrennslisstofn og leysir, lausn
(a.e. = alþjóðlegar einingar)
Voncento 500 a.e. FVIII / 1200 a.e. VWF (10 ml leysir)
stungulyfs-/innrennslisstofn og leysir, lausn
(a.e. = alþjóðlegar einingar)
Voncento 500 a.e. FVIII / 1200 a.e. VWF (5 ml leysir)
stungulyfs-/innrennslisstofn og leysir, lausn
(a.e. = alþjóðlegar einingar)
Voncento 1000 a.e. FVIII / 2400 a.e. VWF (10 ml leysir)
stungulyfs-/innrennslisstofn og leysir, lausn
(a.e. = alþjóðlegar einingar)
2.
INNIHALDSLÝSING
Voncento 250 a.e. FVIII / 600 a.e. VWF stungulyfs-/innrennslisstofn og
leysir, lausn
Hvert hettuglas af stofni inniheldur:
-
250 a.e.* af storkuþætti VIII (coagulation factor VIII, FVIII) úr
mönnum**.
-
600 a.e.*** af von Willebrand þætti (von Willebrand factor, VWF) úr
mönnum**.
Eftir blöndun með meðfylgjandi 5 ml af vatni fyrir stungulyf
inniheldur lausnin 50 a.e./ml af FVIII og
120 a.e./ml af VWF.
Voncento 500 a.e. FVIII / 1200 a.e. VWF stungulyfs-/innrennslisstofn
og leysir, lausn
Hvert hettuglas af stofni inniheldur:
-
500 a.e.* af storkuþætti VIII (coagulation factor VIII, FVIII) úr
mönnum**.
-
1200 a.e.*** af von Willebrand þætti (von Willebrand factor, VWF)
úr mönnum**.
Eftir blöndun með meðfylgjandi 10 ml af vatni fyrir stungulyf
inniheldur lausnin 50 a.e./ml af FVIII
og 120 a.e./ml af VWF.
Voncento 500 a.e. FVIII / 1200 a.e. VWF stungulyfs-/innrennslisstofn
og leysir, lausn
Hvert hettuglas af stofni inniheldur:
-
500 a.e.* af storkuþætti VIII (coagulation factor VIII, FVIII) úr
mönnum**.
-
1200 a.e.*** af von Willebrand þætti (von Willebrand factor, VWF)
úr mönnum**.
Eftir blöndun með meðfylgjandi 5 ml af vatni fyrir stungulyf
inniheldur lausnin 100 a.e./ml af FVIII
og 240 a.e./ml af VWF.
Voncento 1000 a.e. FVIII / 2400 a.e. VWF stungulyfs-/innrennslisstofn
og leysir, lausn
Hvert hettuglas af stofni inniheldur:
-
1000 a.e.* af storkuþætti VIII (coagulation factor VIII
                                
                                Read the complete document
                                
                            

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Summary of Product characteristics Summary of Product characteristics Bulgarian 13-05-2022
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Patient Information leaflet Patient Information leaflet German 13-05-2022
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Public Assessment Report Public Assessment Report Estonian 16-01-2018
Patient Information leaflet Patient Information leaflet Greek 13-05-2022
Public Assessment Report Public Assessment Report Greek 16-01-2018
Patient Information leaflet Patient Information leaflet English 13-05-2022
Public Assessment Report Public Assessment Report English 16-01-2018
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Public Assessment Report Public Assessment Report French 16-01-2018
Patient Information leaflet Patient Information leaflet Italian 13-05-2022
Public Assessment Report Public Assessment Report Italian 16-01-2018
Patient Information leaflet Patient Information leaflet Latvian 13-05-2022
Public Assessment Report Public Assessment Report Latvian 16-01-2018
Patient Information leaflet Patient Information leaflet Lithuanian 13-05-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 13-05-2022
Public Assessment Report Public Assessment Report Lithuanian 16-01-2018
Patient Information leaflet Patient Information leaflet Hungarian 13-05-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 13-05-2022
Public Assessment Report Public Assessment Report Hungarian 16-01-2018
Patient Information leaflet Patient Information leaflet Maltese 13-05-2022
Public Assessment Report Public Assessment Report Maltese 16-01-2018
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Public Assessment Report Public Assessment Report Polish 16-01-2018
Patient Information leaflet Patient Information leaflet Portuguese 13-05-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 13-05-2022
Public Assessment Report Public Assessment Report Portuguese 16-01-2018
Patient Information leaflet Patient Information leaflet Romanian 13-05-2022
Public Assessment Report Public Assessment Report Romanian 16-01-2018
Patient Information leaflet Patient Information leaflet Slovak 13-05-2022
Public Assessment Report Public Assessment Report Slovak 16-01-2018
Patient Information leaflet Patient Information leaflet Slovenian 13-05-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 13-05-2022
Public Assessment Report Public Assessment Report Slovenian 16-01-2018
Patient Information leaflet Patient Information leaflet Finnish 13-05-2022
Public Assessment Report Public Assessment Report Finnish 16-01-2018
Patient Information leaflet Patient Information leaflet Swedish 13-05-2022
Public Assessment Report Public Assessment Report Swedish 16-01-2018
Patient Information leaflet Patient Information leaflet Norwegian 13-05-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 13-05-2022
Patient Information leaflet Patient Information leaflet Croatian 13-05-2022
Public Assessment Report Public Assessment Report Croatian 16-01-2018

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