Ketoconazole HRA

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

Ketoconazole

Available from:

HRA Pharma Rare Diseases

ATC code:

J02AB02

INN (International Name):

ketoconazole

Therapeutic group:

Antimikotiċi għal użu sistemiku

Therapeutic area:

Is-Sindromu ta 'Cushing

Therapeutic indications:

Ketoconazole HRA huwa indikat għat-trattament tas-sindrome endoġenu ta 'Cushing f'adulti u adolexxenti' l fuq minn 12-il sena.

Product summary:

Revision: 10

Authorization status:

Awtorizzat

Authorization date:

2014-11-18

Patient Information leaflet

                                32
B. FULJETT TA’ TAGĦRIF
33
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-PAZJENT
KETOCONAZOLE HRA 200 MG PILLOLI
ketoconazole
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 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, anki jekk ikollhom 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 Ketoconazole HRA u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tieħu Ketoconazole HRA
3.
Kif għandek tieħu Ketoconazole HRA
4.
Effetti sekondarji possibbli
5.
Kif taħżen Ketoconazole HRA
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU KETOCONAZOLE HRA U GĦALXIEX JINTUŻA
Ketoconazole HRA huwa mediċina li fiha s-sustanza attiva ketoconazole
b’attività antikortikosterojde. Jintuża
għall-kura tas-sindrome endoġenu ta’ Cushing (meta l-ġisem
jipproduċi eċċess ta’ kortisol) f’persuni adulti u
adolexxenti minn 12-il sena ’l fuq.
Is-sindrome ta’ Cushing huwa kkawżat minn produzzjoni eċċessiva
ta’ ormon imsejjaħ kortisol li jiġi prodott
mill-glandoli adrenali. Ketoconazole HRA huwa kapaċi jimblokka
l-attività tal-enzimi responsabbli għas-
sintesi tal-kortisol u konsegwentement huwa kapaċi jnaqqas
il-produzzjoni eċċessiva tal-kortisol mill-ġisem
tiegħe
                                
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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 dwar il-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
Ketoconazole HRA 200 mg pilloli
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Kull pillola fiha 200 mg ketoconazole.
Eċċipjent b’effett magħruf:
Kull pillola fiha 19 mg ta’ lactose (bħala monohydrate).
Għal-lista kompluta ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Pillola.
Offwajt għal lewn il-krema ċar, tonda, b’dijametru ta’ 10 mm,
bikonvessa.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Ketoconazole HRA huwa indikat għall-kura tas-sindrome endoġenu ta’
Cushing f’persuni adulti u adolexxenti
minn 12-il sena ’l fuq.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Il-kura għandha tinbeda u tiġi sorveljata minn tobba li jkollhom
esperjenza fl-endokrinoloġija jew il-mediċina
interna u li jkollhom il-faċilitajiet xierqa għall-monitoraġġ
tar-reazzjonijiet bijokimiċi billi d-doża trid tiġi
aġġustata biex tilħaq il-ħtieġa terapewtika tal-pazjent, abbażi
tan-normalizzazzjoni tal-livelli tal-kortisol.
Pożoloġija
_Bidu _
Id-doża rakkomandata fil-bidu fl-adulti u l-adolexxenti hija 400-600
mg/jum meħuda b’mod orali f’żewġ jew
tliet dożi maqsumin u din id-doża tista’ tiżdied malajr għal
800-1,200 mg/jum f’żewġ jew tliet dożi maqsumin.
Fil-bidu tal-kura, kull ftit jiem/ġimgħat għandu jiġi kkontrollat
li ma jkunx hemm kortisol għal 24 siegħa fl-
awrina.
_Aġġustament tal-pożoloġija _
Id-doża ta’ kuljum ta’ ketoconazole għandha tiġi aġġustata
b’mod perjodiku fuq bażi individwali bil-għan li
jiġu normalizzati l-livelli tal-kortisol liberu fl-awrina u/jew
tal-kortisol fil-plażma.
3
-
T
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 07-06-2021
Summary of Product characteristics Summary of Product characteristics Bulgarian 07-06-2021
Public Assessment Report Public Assessment Report Bulgarian 30-01-2015
Patient Information leaflet Patient Information leaflet Spanish 07-06-2021
Public Assessment Report Public Assessment Report Spanish 30-01-2015
Patient Information leaflet Patient Information leaflet Czech 07-06-2021
Public Assessment Report Public Assessment Report Czech 30-01-2015
Patient Information leaflet Patient Information leaflet Danish 07-06-2021
Public Assessment Report Public Assessment Report Danish 30-01-2015
Patient Information leaflet Patient Information leaflet German 07-06-2021
Public Assessment Report Public Assessment Report German 30-01-2015
Patient Information leaflet Patient Information leaflet Estonian 07-06-2021
Public Assessment Report Public Assessment Report Estonian 30-01-2015
Patient Information leaflet Patient Information leaflet Greek 07-06-2021
Public Assessment Report Public Assessment Report Greek 30-01-2015
Patient Information leaflet Patient Information leaflet English 07-06-2021
Public Assessment Report Public Assessment Report English 30-01-2015
Patient Information leaflet Patient Information leaflet French 07-06-2021
Public Assessment Report Public Assessment Report French 30-01-2015
Patient Information leaflet Patient Information leaflet Italian 07-06-2021
Public Assessment Report Public Assessment Report Italian 30-01-2015
Patient Information leaflet Patient Information leaflet Latvian 07-06-2021
Public Assessment Report Public Assessment Report Latvian 30-01-2015
Patient Information leaflet Patient Information leaflet Lithuanian 07-06-2021
Summary of Product characteristics Summary of Product characteristics Lithuanian 07-06-2021
Public Assessment Report Public Assessment Report Lithuanian 30-01-2015
Patient Information leaflet Patient Information leaflet Hungarian 07-06-2021
Summary of Product characteristics Summary of Product characteristics Hungarian 07-06-2021
Public Assessment Report Public Assessment Report Hungarian 30-01-2015
Patient Information leaflet Patient Information leaflet Dutch 07-06-2021
Public Assessment Report Public Assessment Report Dutch 30-01-2015
Patient Information leaflet Patient Information leaflet Polish 07-06-2021
Public Assessment Report Public Assessment Report Polish 30-01-2015
Patient Information leaflet Patient Information leaflet Portuguese 07-06-2021
Summary of Product characteristics Summary of Product characteristics Portuguese 07-06-2021
Public Assessment Report Public Assessment Report Portuguese 30-01-2015
Patient Information leaflet Patient Information leaflet Romanian 07-06-2021
Public Assessment Report Public Assessment Report Romanian 30-01-2015
Patient Information leaflet Patient Information leaflet Slovak 07-06-2021
Public Assessment Report Public Assessment Report Slovak 30-01-2015
Patient Information leaflet Patient Information leaflet Slovenian 07-06-2021
Summary of Product characteristics Summary of Product characteristics Slovenian 07-06-2021
Public Assessment Report Public Assessment Report Slovenian 30-01-2015
Patient Information leaflet Patient Information leaflet Finnish 07-06-2021
Public Assessment Report Public Assessment Report Finnish 30-01-2015
Patient Information leaflet Patient Information leaflet Swedish 07-06-2021
Public Assessment Report Public Assessment Report Swedish 30-01-2015
Patient Information leaflet Patient Information leaflet Norwegian 07-06-2021
Summary of Product characteristics Summary of Product characteristics Norwegian 07-06-2021
Patient Information leaflet Patient Information leaflet Icelandic 07-06-2021
Summary of Product characteristics Summary of Product characteristics Icelandic 07-06-2021
Patient Information leaflet Patient Information leaflet Croatian 07-06-2021
Public Assessment Report Public Assessment Report Croatian 30-01-2015

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