Elfabrio

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

Pegunigalsidase alfa

Available from:

Chiesi Farmaceutici S.p.A

ATC code:

A16AB20

INN (International Name):

pegunigalsidase alfa

Therapeutic group:

Oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti,

Therapeutic area:

Marda ta 'Fabry

Therapeutic indications:

Elfabrio is indicated for long-term enzyme replacement therapy in adult patients with a confirmed diagnosis of Fabry disease (deficiency of alpha-galactosidase).

Product summary:

Revision: 1

Authorization status:

Awtorizzat

Authorization date:

2023-05-04

Patient Information leaflet

                                22
B. FULJETT TA’ TAGĦRIF
23
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-UTENT
ELFABRIO 2 MG/ML KONĊENTRAT GĦAL SOLUZZJONI GĦALL-INFUŻJONI
pegunigalsidase alfa
Dan il-prodott mediċinali huwa suġġett għal monitoraġġ
addizzjonali. Dan ser jippermetti
identifikazzjoni ta’ malajr ta’ informazzjoni ġdida dwar
is-sigurtà. Inti tista’ tgħin billi tirrapporta
kwalunkwe effett sekondarju li jista’ jkollok. Ara t-tmiem ta’
sezzjoni 4 biex tara kif għandek
tirrapporta effetti sekondarji.
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 jew lill-ispiżjar
tiegħek.
-
Din il-mediċina ġiet mogħtija lilek biss. M’għandekx tgħaddiha
lil persuni oħra. Tista’
tagħmlilhom il-ħsara anke jekk għandhom l-istess sinjali ta’ mard
bħal tiegħek.
-
Jekk ikollok xi effett sekondarju kellem lit-tabib jew lill-ispiżjar
tiegħek. Dan jinkludi xi effett
sekondarju possibbli li mhuwiex elenkat f’dan il-fuljett. Ara
sezzjoni 4.
F’DAN IL-FULJETT
1.
X’inhu Elfabrio u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tingħata Elfabrio
3.
Kif jingħata Elfabrio
4.
Effetti sekondarji possibbli
5.
Kif taħżen Elfabrio
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU ELFABRIO U GĦALXIEX JINTUŻA
Elfabrio fih is-sustanza attiva pegunigalsidase alfa, u jintuża
bħala terapija ta’ sostituzzjoni tal-enżimi
f’pazjenti adulti bil-marda ta’ Fabry ikkonfermata. Il-marda ta’
Fabry hija marda ġenetika rari li tista’
taffettwa ħafna partijiet tal-ġisem. F’pazjenti bil-marda ta’
Fabry, sustanza ta’ xaħam ma titneħħiex
miċ-ċelluli ta’ ġisimhom, u takkumula fil-ħitan tal-kanali
tad-demm u dan jista’ jwassal għal
insuffiċjenza tal-organi. Dan ix-xaħam jakkumula fiċ-ċelluli ta’
dawn il-pazjenti minħabba li
m’għandhomx biżżejjed enżima msejħa α-galactosidase-A,
l-enżima respons
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
Dan il-prodott mediċinali huwa suġġett għal monitoraġġ
addizzjonali. Dan ser jippermetti
identifikazzjoni ta’ malajr ta’ informazzjoni ġdida dwar
is-sigurtà. Il-professjonisti tal-kura tas-saħħa
huma mitluba jirrappurtaw kwalunkwe reazzjoni avversa suspettata. Ara
sezzjoni 4.8 dwar kif
għandhom jiġu rappurtati reazzjonijiet avversi.
1.
ISEM IL-PRODOTT MEDIĊINALI
Elfabrio 2 mg/mL konċentrat għal soluzzjoni għall-infużjoni
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Kull kunjett fih 20 mg ta’ pegunigalsidase alfa f’volum ta’ 10
mL f’konċentrazzjoni ta’ 2 mg/mL.
Il-qawwa tindika l-kwantità ta’ pegunigalsidase alfa
b’konsiderazzjoni tal-pegilazzjoni.
Pegunigalsidase alfa huwa magħmul fiċ-ċelluli tat-tabakk (ċelluli
_Nicotiana tabacum_ BY2) permezz
ta’ teknoloġija rikombinanti tad-DNA.
Is-sustanza attiva, pegunigalsidase alfa, hija konjugat kovalenti
ta’ prh-alpha-GAL-A ma’
polyethylene glycol (PEG).
Il-qawwa ta’ dan il-prodott mediċinali m’għandhiex titqabbel
ma’ dik ta’ proteina pegilata jew mhux
pegilata oħra tal-istess klassi terapewtika. Għal aktar
informazzjoni, ara sezzjoni 5.1.
Eċċipjent b’effett magħruf
Kull kunjett fih 48 mg ta’ sodium.
Għal-lista sħiħa ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Konċentrat għal soluzzjoni għall-infużjoni
Soluzzjoni ċara u bla kulur.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Elfabrio huwa indikat għal terapija ta’ sostituzzjoni tal-enżimi
fit-tul f’pazjenti adulti b’dijanjosi
kkonfermata tal-marda ta’ Fabry (defiċjenza ta’
alpha-galactosidase).
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
It-trattament b’Elfabrio irid jiġi mmaniġġjat minn tabib
b’esperjenza fit-trattament ta’ pazjenti bil-
marda ta’ Fabry.
Miżuri xierqa ta’ appoġġ mediku għandhom ikunu disponibbli
fil-pront meta Elfabrio jingħata lil
pazjenti li qatt ma kienu ħadu trattament qabel, jew li kellhom
reazzjonijiet seve
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 08-05-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 08-05-2023
Public Assessment Report Public Assessment Report Bulgarian 08-05-2023
Patient Information leaflet Patient Information leaflet Spanish 08-05-2023
Public Assessment Report Public Assessment Report Spanish 08-05-2023
Patient Information leaflet Patient Information leaflet Czech 08-05-2023
Public Assessment Report Public Assessment Report Czech 08-05-2023
Patient Information leaflet Patient Information leaflet Danish 08-05-2023
Public Assessment Report Public Assessment Report Danish 08-05-2023
Patient Information leaflet Patient Information leaflet German 08-05-2023
Public Assessment Report Public Assessment Report German 08-05-2023
Patient Information leaflet Patient Information leaflet Estonian 08-05-2023
Public Assessment Report Public Assessment Report Estonian 08-05-2023
Patient Information leaflet Patient Information leaflet Greek 08-05-2023
Public Assessment Report Public Assessment Report Greek 08-05-2023
Patient Information leaflet Patient Information leaflet English 08-05-2023
Public Assessment Report Public Assessment Report English 08-05-2023
Patient Information leaflet Patient Information leaflet French 08-05-2023
Public Assessment Report Public Assessment Report French 08-05-2023
Patient Information leaflet Patient Information leaflet Italian 08-05-2023
Public Assessment Report Public Assessment Report Italian 08-05-2023
Patient Information leaflet Patient Information leaflet Latvian 08-05-2023
Public Assessment Report Public Assessment Report Latvian 08-05-2023
Patient Information leaflet Patient Information leaflet Lithuanian 08-05-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 08-05-2023
Public Assessment Report Public Assessment Report Lithuanian 08-05-2023
Patient Information leaflet Patient Information leaflet Hungarian 08-05-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 08-05-2023
Public Assessment Report Public Assessment Report Hungarian 08-05-2023
Patient Information leaflet Patient Information leaflet Dutch 08-05-2023
Public Assessment Report Public Assessment Report Dutch 08-05-2023
Patient Information leaflet Patient Information leaflet Polish 08-05-2023
Public Assessment Report Public Assessment Report Polish 08-05-2023
Patient Information leaflet Patient Information leaflet Portuguese 08-05-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 08-05-2023
Public Assessment Report Public Assessment Report Portuguese 08-05-2023
Patient Information leaflet Patient Information leaflet Romanian 08-05-2023
Public Assessment Report Public Assessment Report Romanian 08-05-2023
Patient Information leaflet Patient Information leaflet Slovak 08-05-2023
Public Assessment Report Public Assessment Report Slovak 08-05-2023
Patient Information leaflet Patient Information leaflet Slovenian 08-05-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 08-05-2023
Public Assessment Report Public Assessment Report Slovenian 08-05-2023
Patient Information leaflet Patient Information leaflet Finnish 08-05-2023
Public Assessment Report Public Assessment Report Finnish 08-05-2023
Patient Information leaflet Patient Information leaflet Swedish 08-05-2023
Public Assessment Report Public Assessment Report Swedish 08-05-2023
Patient Information leaflet Patient Information leaflet Norwegian 08-05-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 08-05-2023
Patient Information leaflet Patient Information leaflet Icelandic 08-05-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 08-05-2023
Patient Information leaflet Patient Information leaflet Croatian 08-05-2023
Public Assessment Report Public Assessment Report Croatian 08-05-2023

Search alerts related to this product

View documents history