Lojuxta

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

Lomitapide

Available from:

Amryt Pharmaceuticals DAC

ATC code:

C10AX12

INN (International Name):

lomitapide

Therapeutic group:

Aġenti li jimmodifikaw il-lipidi

Therapeutic area:

Iperkolesterolemija

Therapeutic indications:

Lojuxta huwa indikat bħala frozen dieta low‑fat u lipid‑lowering prodotti mediċinali oħra jew mingħajru baxxa density-lipoprotein (LDL) aferesi fil-pazjenti adulti ma hypercholesterolaemia homozygous familjari (HoFH). Ġenetiċi-konferma tal-HoFH għandu jinkiseb kull meta jkun possibbli. - Forom l-oħra tal-primarja hyperlipoproteinaemia u l-kawżi sekondarji ta ' l-iperkolesterolimja (e. sindromu nefrotiku, ipotirojdiżmu) għandhom jiġu esklużi.

Product summary:

Revision: 18

Authorization status:

Awtorizzat

Authorization date:

2013-07-31

Patient Information leaflet

                                35
B. FULJETT TA’ TAGĦRIF
36
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-UTENT
LOJUXTA 5 MG KAPSULI IBSIN
LOJUXTA 10 MG KAPSULI IBSIN
LOJUXTA 20 MG KAPSULI IBSIN
lomitapide
Dan il-prodott mediċinali huwa soġġett 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 TIEĦU 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
s-sezzjoni 4.
F’DAN IL-FULJETT
1.
X’inhu Lojuxta u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tieħu Lojuxta
3.
Kif għandek tieħu Lojuxta
4.
Effetti sekondarji possibbli
5.
Kif taħżen Lojuxta
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU LOJUXTA U GĦALXIEX JINTUŻA
Lojuxta fih is-sustanza attiva msejħa lomitapide. Lomitapide huwa
“aġent li jimmodifika l-lipidi” li
jaħdem billi jimblokka l-azzjoni ta’ “proteina tat-trasferiment
mikrosomali tat-trigliċeridi.” Din il-
proteina tinstab fiċ-ċelloli tal-fwied u tal-imsaren, fejn hija
involuta fil-bini ta’ sustanzi xaħmin
f’partikoli akbar li mbagħad jiġu rilaxxati fid-demm. Billi
timblokka din il-proteina, il-mediċina
tnaqqas il-livell ta’ xaħam u ta’ kolesterol (lipidi) fid-demm.
Lojuxta jintuża fil-kura ta’ pazjenti adulti b’kolesterol għoli
ħafna minħabba kundizzjoni fil-familji
tagħ
                                
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Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
Dan il-prodott mediċinali huwa soġġett għal monitoraġġ
addizzjonali. Dan ser jippermetti
identifikazzjoni ta’ malajr ta’ informazzjoni ġdida dwar
is-sigurtà. Il-professjonisti dwar il-kura
tas-saħħa huma mitluba jirrappurtaw kwalunkwe reazzjoni avversa
suspettata. Ara s-sezzjoni 4.8 dwar
kif għandhom jiġu rappurtati reazzjonijiet avversi.
1.
ISEM IL-PRODOTT MEDIĊINALI_ _
_ _
Lojuxta 5 mg kapsuli ibsin
Lojuxta 10 mg kapsuli ibsin
_ _
Lojuxta 20 mg kapsuli ibsin
Lojuxta 30 mg kapsuli ibsin
Lojuxta 40 mg kapsuli ibsin
Lojuxta 60 mg kapsuli ibsin
_ _
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Lojuxta 5 m
g kapsuli ibsin
Kull kapsula iebsa fiha lomitapide mesylate ekwivalenti għal 5 mg
ta’ lomitapide.
_Eċċipjent(i) b’effett magħruf _
Kull kapsula iebsa fiha 70.12 mg ta’ lattożju (bħala monoidrat)
(ara s-sezzjoni 4.4).
Lojuxta 10 m
g kapsuli ibsin
Kull kapsula iebsa fiha lomitapide mesylate ekwivalenti għal 10 mg
ta’ lomitapide.
_Eċċipjent(i) b’effett magħruf _
Kull kapsula iebsa fiha 140.23 mg ta’ lattożju (bħala monoidrat)
(ara s-sezzjoni 4.4).
Lojuxta 20 m
g kapsuli ibsin
Kull kapsula iebsa fiha lomitapide mesylate ekwivalenti għal 20 mg
ta’ lomitapide.
_Eċċipjent(i) b’effett magħruf _
Kull kapsula iebsa fiha 129.89 mg ta’ lattożju (bħala monoidrat)
(ara s-sezzjoni 4.4).
Lojuxta 30 m
g kapsuli ibsin
Kull kapsula iebsa fiha lomitapide mesylate ekwivalenti għal 30 mg
ta’ lomitapide.
_Eċċipjent(i) b’effett magħruf _
Kull kapsula iebsa fiha 194.84 mg ta’ lattożju (bħala monoidrat)
(ara s-sezzjoni 4.4).
Lojuxta 40 m
g kapsuli ibsin
Kull kapsula iebsa fiha lomitapide mesylate ekwivalenti għal 40 mg
ta’ lomitapide.
_Eċċipjent(i) b’effett magħruf _
Kull kapsula iebsa fiha 259.79 mg ta’ lattożju (bħala monoidrat)
(ara s-sezzjoni 4.4).
Lojuxta 60 m
g kapsuli ibsin
Kull kapsula iebsa fiha lomitapide mesylate ekwivalenti għal 60 mg
ta’ lomitapide.
3
_Eċċipjent(i) b’effett magħruf _
Kull kapsula
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 06-11-2023
Public Assessment Report Public Assessment Report Bulgarian 11-03-2016
Patient Information leaflet Patient Information leaflet Spanish 06-11-2023
Public Assessment Report Public Assessment Report Spanish 11-03-2016
Patient Information leaflet Patient Information leaflet Czech 06-11-2023
Public Assessment Report Public Assessment Report Czech 11-03-2016
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Public Assessment Report Public Assessment Report Danish 11-03-2016
Patient Information leaflet Patient Information leaflet German 06-11-2023
Public Assessment Report Public Assessment Report German 11-03-2016
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Public Assessment Report Public Assessment Report Estonian 11-03-2016
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Public Assessment Report Public Assessment Report Greek 11-03-2016
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Public Assessment Report Public Assessment Report English 11-03-2016
Patient Information leaflet Patient Information leaflet French 06-11-2023
Public Assessment Report Public Assessment Report French 11-03-2016
Patient Information leaflet Patient Information leaflet Italian 06-11-2023
Public Assessment Report Public Assessment Report Italian 11-03-2016
Patient Information leaflet Patient Information leaflet Latvian 06-11-2023
Public Assessment Report Public Assessment Report Latvian 11-03-2016
Patient Information leaflet Patient Information leaflet Lithuanian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 06-11-2023
Public Assessment Report Public Assessment Report Lithuanian 11-03-2016
Patient Information leaflet Patient Information leaflet Hungarian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 06-11-2023
Public Assessment Report Public Assessment Report Hungarian 11-03-2016
Patient Information leaflet Patient Information leaflet Dutch 06-11-2023
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Patient Information leaflet Patient Information leaflet Polish 06-11-2023
Public Assessment Report Public Assessment Report Polish 11-03-2016
Patient Information leaflet Patient Information leaflet Portuguese 06-11-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 06-11-2023
Public Assessment Report Public Assessment Report Portuguese 11-03-2016
Patient Information leaflet Patient Information leaflet Romanian 06-11-2023
Public Assessment Report Public Assessment Report Romanian 11-03-2016
Patient Information leaflet Patient Information leaflet Slovak 06-11-2023
Public Assessment Report Public Assessment Report Slovak 11-03-2016
Patient Information leaflet Patient Information leaflet Slovenian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 06-11-2023
Public Assessment Report Public Assessment Report Slovenian 11-03-2016
Patient Information leaflet Patient Information leaflet Finnish 06-11-2023
Public Assessment Report Public Assessment Report Finnish 11-03-2016
Patient Information leaflet Patient Information leaflet Swedish 06-11-2023
Public Assessment Report Public Assessment Report Swedish 11-03-2016
Patient Information leaflet Patient Information leaflet Norwegian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 06-11-2023
Patient Information leaflet Patient Information leaflet Icelandic 06-11-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 06-11-2023
Patient Information leaflet Patient Information leaflet Croatian 06-11-2023
Public Assessment Report Public Assessment Report Croatian 11-03-2016

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