Vpriv

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

velagluceraza alfa

Available from:

Takeda Pharmaceuticals International AG Ireland Branch

ATC code:

A16AB10

INN (International Name):

velaglucerase alfa

Therapeutic group:

Drugi zdravljene bolezni prebavil in presnove izdelki,

Therapeutic area:

Gaucher bolezen

Therapeutic indications:

Vpriv je indiciran za dolgoročno encimsko nadomestno zdravljenje (ERT) pri bolnikih z Gaucherjevo boleznijo tipa 1.

Product summary:

Revision: 20

Authorization status:

Pooblaščeni

Authorization date:

2010-08-26

Patient Information leaflet

                                22
Po rekonstituciji in redčenju
Uporabite takoj. Ne shranjujte dlje kot 24 ur pri temperaturi od 2

C do 8

C.
9.
POSEBNA NAVODILA ZA SHRANJEVANJE
Shranjujte v hladilniku.
Ne zamrzujte.
Vialo shranjujte v zunanji škatli za zagotovitev zaščite pred
svetlobo.
10.
POSEBNI VARNOSTNI UKREPI ZA ODSTRANJEVANJE NEUPORABLJENIH
ZDRAVIL ALI IZ NJIH NASTALIH ODPADNIH SNOVI, KADAR SO POTREBNI
Ne uporabljajte, če je raztopina obarvana ali če so v njej prisotni
vidni tujki.
11.
IME IN NASLOV IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
Takeda Pharmaceuticals International AG Ireland Branch
Block 2 Miesian Plaza
50-58 Baggot Street Lower
Dublin 2
D02 HW68
Irska
12.
Š
TEVILKA(E) DOVOLJENJA (DOVOLJENJ) ZA PROMET
EU/1/10/646/002
13.
Š
TEVILKA SERIJE
Serija
14.
NAČIN IZDAJANJA ZDRAVILA
15.
NAVODILA ZA UPORABO
16.
PODATKI V BRAILLOVI PISAVI
Sprejeta je utemeljitev, da Braillova pisava ni potrebna.
17.
EDINSTVENA OZNAKA – DVODIMENZIONALNA ČRTNA KODA
Vsebuje dvodimenzionalno črtno kodo z edinstveno oznako.
23
18.
EDINSTVENA OZNAKA – V BERLJIVI OBLIKI
PC
SN
NN
24
PODATKI NA ZUNANJI OVOJNINI
ZUNANJA
Š
KATLA – 400 ENOT (PAKIRANJE S 5 VIALAMI)
1.
IME ZDRAVILA
VPRIV 400 enot prašek za raztopino za infundiranje
velagluceraza alfa
2.
NAVEDBA ENE ALI VEČ UČINKOVIN
Ena viala vsebuje 400 enot velagluceraze alfa.
Po rekonstituciji en ml raztopine vsebuje 100 enot velagluceraze alfa.
3.
SEZNAM POMO
Ž
NIH SNOVI
Vsebuje tudi:
saharozo
natrijev citrat, dihidrat
monohidrat citronske kisline
polisorbat 20
Dodatne informacije so v navodilu.
4.
FARMACEVTSKA OBLIKA IN VSEBINA
Prašek za raztopino za infundiranje
5 vial
5.
POSTOPEK IN POT(I) UPORABE ZDRAVILA
Samo za enkratno uporabo.
Pred uporabo preberite priloženo navodilo!
Intravenska uporaba
6.
POSEBNO OPOZORILO O SHRANJEVANJU ZDRAVILA ZUNAJ DOSEGA IN
POGLEDA OTROK
Zdravilo shranjujte nedosegljivo otrokom!
7.
DRUGA POSEBNA OPOZORILA, ČE SO POTREBNA
8.
DATUM IZTEKA ROKA UPORABNOSTI ZDRAVILA
Uporabno do
25
Po rekonstituciji in redčenju
Uporabite takoj. Ne shranjujte dlje kot 
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
PRILOGA I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
2
1.
IME ZDRAVILA
VPRIV 400 enot prašek za raztopino za infundiranje
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Ena viala vsebuje 400 enot* velagluceraze alfa**.
Po rekonstituciji en ml raztopine vsebuje 100 enot velagluceraze alfa.
* Encimska enota je opredeljena kot količina encima, potrebna za
pretvorbo enega mikromola
p-nitrofenil ß-D-glukopiranozida v p-nitrofenol na minuto pri 37 ºC.
** Izdelano s tehnologijo rekombinantne DNA v humani fibroblastni
celični liniji HT-1080.
Pomožna(e) snov(i) z znanim učinkom:
Ena viala vsebuje 12,15 mg natrija.
Za celoten seznam pomožnih snovi glejte poglavje 6.1.
3.
FARMACEVTSKA OBLIKA
prašek za raztopino za infundiranje
Bel ali belkast prašek.
4.
KLINIČNI PODATKI
4.1
TERAPEVTSKE INDIKACIJE
Zdravilo VPRIV je indicirano za dolgoročno nadomestno encimsko
zdravljenje (NEZ) bolnikov z
Gaucherjevo boleznijo tipa 1.
4.2
ODMERJANJE IN NAČIN UPORABE
Zdravljenje z zdravilom VPRIV mora nadzirati zdravnik z izkušnjami
pri obravnavanju bolnikov z
Gaucherjevo boleznijo.
Odmerjanje
Priporočeni odmerek je 60 enot/kg, vsak drugi teden.
Prilagoditve odmerka se lahko izvedejo za vsakega posameznika posebej
na podlagi doseganja in
vzdrževanja terapevtskih ciljev. V kliničnih študijah so ocenili
odmerke od 15 do 60 enot/kg vsak
drugi teden. Študij z odmerki, večjimi od 60 enot/kg, niso izvedli.
Bolniki, ki trenutno prejemajo nadomestno encimsko zdravljenje z
imiglucerazo za Gaucherjevo
bolezen tipa 1, lahko preidejo na zdravilo VPRIV, pri čemer se
uporabita enak odmerek in pogostnost
uporabe.
Posebne populacije
_Starejši bolniki (stari ≥ 65 let) _
Starejši bolniki se lahko zdravijo z enakim razponom odmerkov (od 15
do 60 enot/kg) kot drugi
odrasli bolniki (glejte poglavje 5.1).
3
Okvara ledvic
Na podlagi trenutnega znanja o farmakokinetiki in farmakodinamiki
velagluceraze alfa prilagoditev
odmerka pri bolnikih z okvaro ledvic ni priporočljiva (glejte
poglavje 5.2).
Okvara jeter
Na podlagi trenutnega znanja o farmakokinetiki
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 08-08-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 08-08-2023
Public Assessment Report Public Assessment Report Bulgarian 01-07-2016
Patient Information leaflet Patient Information leaflet Spanish 08-08-2023
Public Assessment Report Public Assessment Report Spanish 01-07-2016
Patient Information leaflet Patient Information leaflet Czech 08-08-2023
Public Assessment Report Public Assessment Report Czech 01-07-2016
Patient Information leaflet Patient Information leaflet Danish 08-08-2023
Public Assessment Report Public Assessment Report Danish 01-07-2016
Patient Information leaflet Patient Information leaflet German 08-08-2023
Public Assessment Report Public Assessment Report German 01-07-2016
Patient Information leaflet Patient Information leaflet Estonian 08-08-2023
Public Assessment Report Public Assessment Report Estonian 01-07-2016
Patient Information leaflet Patient Information leaflet Greek 08-08-2023
Public Assessment Report Public Assessment Report Greek 01-07-2016
Patient Information leaflet Patient Information leaflet English 08-08-2023
Public Assessment Report Public Assessment Report English 01-07-2016
Patient Information leaflet Patient Information leaflet French 08-08-2023
Public Assessment Report Public Assessment Report French 01-07-2016
Patient Information leaflet Patient Information leaflet Italian 08-08-2023
Public Assessment Report Public Assessment Report Italian 01-07-2016
Patient Information leaflet Patient Information leaflet Latvian 08-08-2023
Public Assessment Report Public Assessment Report Latvian 01-07-2016
Patient Information leaflet Patient Information leaflet Lithuanian 08-08-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 08-08-2023
Public Assessment Report Public Assessment Report Lithuanian 01-07-2016
Patient Information leaflet Patient Information leaflet Hungarian 08-08-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 08-08-2023
Public Assessment Report Public Assessment Report Hungarian 01-07-2016
Patient Information leaflet Patient Information leaflet Maltese 08-08-2023
Public Assessment Report Public Assessment Report Maltese 01-07-2016
Patient Information leaflet Patient Information leaflet Dutch 08-08-2023
Public Assessment Report Public Assessment Report Dutch 01-07-2016
Patient Information leaflet Patient Information leaflet Polish 08-08-2023
Public Assessment Report Public Assessment Report Polish 01-07-2016
Patient Information leaflet Patient Information leaflet Portuguese 08-08-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 08-08-2023
Public Assessment Report Public Assessment Report Portuguese 01-07-2016
Patient Information leaflet Patient Information leaflet Romanian 08-08-2023
Public Assessment Report Public Assessment Report Romanian 01-07-2016
Patient Information leaflet Patient Information leaflet Slovak 08-08-2023
Public Assessment Report Public Assessment Report Slovak 01-07-2016
Patient Information leaflet Patient Information leaflet Finnish 08-08-2023
Public Assessment Report Public Assessment Report Finnish 01-07-2016
Patient Information leaflet Patient Information leaflet Swedish 08-08-2023
Public Assessment Report Public Assessment Report Swedish 01-07-2016
Patient Information leaflet Patient Information leaflet Norwegian 08-08-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 08-08-2023
Patient Information leaflet Patient Information leaflet Icelandic 08-08-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 08-08-2023
Patient Information leaflet Patient Information leaflet Croatian 08-08-2023
Public Assessment Report Public Assessment Report Croatian 01-07-2016

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