Evicel

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

fibrinoġen uman, trombina umana

Available from:

Omrix Biopharmaceuticals N. V.

ATC code:

B02BC

INN (International Name):

human fibrinogen, human thrombin

Therapeutic group:

Sustanzi kontra l-emorraġija

Therapeutic area:

Hemostasi, kirurġiċi

Therapeutic indications:

Evicel jintuża bħala kura ta 'appoġġ fil-kirurġija fejn it-tekniki kirurġiċi standard mhumiex biżżejjed, għal titjib fl-emostasi. Evicel huwa wkoll indikat bħala appoġġ għas-sutura għall-emostażi f'kirurġija vaskulari.

Product summary:

Revision: 18

Authorization status:

Awtorizzat

Authorization date:

2008-10-05

Patient Information leaflet

                                23
B. FULJETT TA’ TAGĦRIF
24
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-UTENT
EVICEL SOLUZZJONIJIET TA’ SIĠILLANT
fibrinoġen uman
trombina umana
AQRA SEW DAN IL-FULJETT KOLLU QABEL TIBDA TUŻA DIN IL-MEDIĊINA
PERESS LI FIH INFORMAZZJONI IMPORTANTI
GĦALIK.
-
Żomm dan il-fuljett. Jista’ jkollok bżonn terġa’ taqrah.
-
Jekk ikollok aktar mistoqsijiet, staqsi lit-tabib tiegħek.
-
Jekk ikollok xi effett sekondarju kellem lit-tabib, lill-ispiżjar jew
l-infermier tiegħek. Dan jinkludi xi
effett sekondarju possibbli li m’huwiex elenkat f’dan il-fuljett.
Ara sezzjoni 4.
F’DAN IL-FULJETT:
1.
X’inhu EVICEL u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tuża EVICEL
3.
Kif għandek tuża EVICEL
4.
Effetti sekondarji possibbli
5.
Kif taħżen EVICEL
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU EVICEL U GĦALXIEX JINTUŻA
EVICEL huwa Siġillant li fih il-Fibrina Umana li huwa fornut bħala
pakkett li fih żewġ kunjetti separati, kull
wieħed fih 1 ml, 2 ml jew 5 ml ta’ soluzzjoni (Fibrinoġen uman u
Trombina umana, rispettivament).
Apparat ta’ applikazzjoni u truf aċċessorji adattati huma fornuti
separatament.
Fibrinoġen huwa konċentrat ta’ proteina li tgħaqqad u t-trombina
hija enzima li tikkawża l-fużjoni
tal-proteina li tgħaqqad. Għalhekk, meta ż-żewġ komponenti
jitħalltu flimkien huma jagħqdu fil-pront.
EVICEL huwa applikat f’adulti waqt operazzjonijiet kirurġiċi biex
inaqqas il-fsada u tnixxija waqt u wara l-
operazzjoni.
EVICEL jista’ jintuża f’kirurġija tal-vażi tad-demm u
kirurġija li sseħħ fuq il-ħajt addominali posterjuri.
EVICEL jista’ jintuża wkoll biex jappoġġja l-għeluq li ma
jippermettix tnixxija ta’ ilma mill-enveloppi
ċerebrali (dura mater) matul newrokirurġija meta tekniki kirurġiċi
oħrajn ikunu insuffiċjenti.
Huwa jitqattar jew jiġi sprejjat għal fuq tessut maqtugħ fejn
jifforma saff irqiq li jissiġilla t-tessut u jwaqqaf
il-fsada.
2.
X’GĦANDEK TKUN TAF QABEL MA TUŻA EVICEL
TUŻAX EVICEL

Jekk inti a
                                
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Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
EVICEL soluzzjonijiet ta’ siġillanti
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Is-sustanzi attivi huma kif ġejjin:
KUNJETT TA’ 1 ML
KUNJETT TA’ 2 ML
KUNJETT TA’ 5 ML
KOMPONENT 1
Proteina umana li tagħqad li fiha
prinċipalment
fibrinoġen
u
fibronektina *
50 – 90 mg
100 – 180 mg
250 – 450 mg
KOMPONENT 2
Trombina umana
800 – 1,200 IU
1,600 – 2,400 IU
4,000 – 6,000 IU
* Il-kwantità totali ta’ proteina hija 80 - 120 mg/ml
Għal-lista kompluta ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Soluzzjonijiet ta’ siġillant.
Soluzzjonijiet ċari jew xi ftit opalexxenti.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
EVICEL huwa indikat f’adulti bħala kura ta’ appoġġ
fil-kirurġija, għal titjib tal-emostażi, fejn tekniċi kirurġiċi
standard mhumiex biżżejjed (ara sezzjoni 5.1).
EVICEL huwa wkoll indikat f’adulti bħala appoġġ għas-sutura
għall-emostażi f’kirurġija vaskulari u għall-
issiġillar ta’ linja ta’ suturi fl-għeluq tad-dura mater.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
L-użu ta’ EVICEL huwa ristrett għall-kirurgi esperti li ġew
imħarrġa fl-użu ta’ EVICEL.
_Pożoloġija_
Il-volum ta’ EVICEL li jrid jiġi applikat u l-frekwenza
tal-applikazzjoni għandhom dejjem ikunu orjentati lejn
il-ħtiġijiet kliniċi bażiċi tal-pazjent.
Id-doża li trid tiġi applikata hija regolata permezz ta’ varjabbli
li jinkludu, iżda mhux limitati għal, it-tip ta’
intervent kirurġiku, id-daqs tal-erja u l-mod ta’ applikazzjoni
intenzjonata u n-numru ta’ applikazzjonijiet.
L-applikazzjoni tal-prodott jeħtieġ li tkun individwalizzata
mit-tabib li jkun qiegħed jagħti t-trattament. Fi
provi kliniċi kkontrollati f’kirurġija vaskulari, id-dożaġġ
individwali użat kien sa 4 ml; għall-issiġillar ta’
linja ta’ suturi fl-għeluq tad-dura mater, intużaw dożi ta’ sa
8 ml, filwaqt li f’kirurġija retroperitoneali u
3
intraddomin
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 11-05-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 11-05-2023
Public Assessment Report Public Assessment Report Bulgarian 17-09-2013
Patient Information leaflet Patient Information leaflet Spanish 11-05-2023
Public Assessment Report Public Assessment Report Spanish 17-09-2013
Patient Information leaflet Patient Information leaflet Czech 11-05-2023
Public Assessment Report Public Assessment Report Czech 17-09-2013
Patient Information leaflet Patient Information leaflet Danish 11-05-2023
Public Assessment Report Public Assessment Report Danish 17-09-2013
Patient Information leaflet Patient Information leaflet German 11-05-2023
Public Assessment Report Public Assessment Report German 17-09-2013
Patient Information leaflet Patient Information leaflet Estonian 11-05-2023
Public Assessment Report Public Assessment Report Estonian 17-09-2013
Patient Information leaflet Patient Information leaflet Greek 11-05-2023
Public Assessment Report Public Assessment Report Greek 17-09-2013
Patient Information leaflet Patient Information leaflet English 11-05-2023
Public Assessment Report Public Assessment Report English 17-09-2013
Patient Information leaflet Patient Information leaflet French 11-05-2023
Public Assessment Report Public Assessment Report French 17-09-2013
Patient Information leaflet Patient Information leaflet Italian 11-05-2023
Public Assessment Report Public Assessment Report Italian 17-09-2013
Patient Information leaflet Patient Information leaflet Latvian 11-05-2023
Public Assessment Report Public Assessment Report Latvian 17-09-2013
Patient Information leaflet Patient Information leaflet Lithuanian 11-05-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 11-05-2023
Public Assessment Report Public Assessment Report Lithuanian 17-09-2013
Patient Information leaflet Patient Information leaflet Hungarian 11-05-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 11-05-2023
Public Assessment Report Public Assessment Report Hungarian 17-09-2013
Patient Information leaflet Patient Information leaflet Dutch 11-05-2023
Public Assessment Report Public Assessment Report Dutch 17-09-2013
Patient Information leaflet Patient Information leaflet Polish 11-05-2023
Public Assessment Report Public Assessment Report Polish 17-09-2013
Patient Information leaflet Patient Information leaflet Portuguese 11-05-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 11-05-2023
Public Assessment Report Public Assessment Report Portuguese 17-09-2013
Patient Information leaflet Patient Information leaflet Romanian 11-05-2023
Public Assessment Report Public Assessment Report Romanian 17-09-2013
Patient Information leaflet Patient Information leaflet Slovak 11-05-2023
Public Assessment Report Public Assessment Report Slovak 17-09-2013
Patient Information leaflet Patient Information leaflet Slovenian 11-05-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 11-05-2023
Public Assessment Report Public Assessment Report Slovenian 17-09-2013
Patient Information leaflet Patient Information leaflet Finnish 11-05-2023
Public Assessment Report Public Assessment Report Finnish 17-09-2013
Patient Information leaflet Patient Information leaflet Swedish 11-05-2023
Public Assessment Report Public Assessment Report Swedish 17-09-2013
Patient Information leaflet Patient Information leaflet Norwegian 11-05-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 11-05-2023
Patient Information leaflet Patient Information leaflet Icelandic 11-05-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 11-05-2023
Patient Information leaflet Patient Information leaflet Croatian 11-05-2023

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