Nitisinone MDK (previously Nitisinone MendeliKABS)

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

nitisinone

Available from:

MendeliKABS Europe Ltd

ATC code:

A16AX04

INN (International Name):

nitisinone

Therapeutic group:

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

Therapeutic area:

Tyrosinemias

Therapeutic indications:

Trattament ta ' l-adulti u paediatric (fi kwalunkwe medda ta ' età) pazjenti ma dijanjosi konfermati ta ' tyrosinemia ereditarji tat-tip 1 (HT 1) flimkien ma ' restrizzjoni tad-dieta ta ' tyrosine u fenilalanina.

Product summary:

Revision: 6

Authorization status:

Irtirat

Authorization date:

2017-08-24

Patient Information leaflet

                                27
B. FULJETT TA’ TAGĦRIF
Prodott mediċinali li m’għadux awtorizzat
28
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-UTENT
NITISINONE MDK 2 MG KAPSULI IEBSIN
NITISINONE MDK 5 MG KAPSULI IEBSIN
NITISINONE MDK 10 MG KAPSULI IEBSIN
NITISINONE MDK 20 MG KAPSULI IEBSIN
nitisinone
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, lill-ispiżjar jew
lill-infermier 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 Nitisinone MDK u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tieħu Nitisinone MDK
3.
Kif għandek tieħu Nitisinone MDK
4.
Effetti sekondarji possibbli
5.
Kif taħżen Nitisinone MDK
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU NITISINONE MDK U GĦALXIEX JINTUŻA
Nitisinone MDK fih is-sustanza attiva nitisinone. Din il-mediċina
tintuża għall-kura ta’ marda rari
msejħa tirosinemija ereditarja tip 1 fl- adulti, adolexxenti u
fit-tfal (f’kull medda ta’ età).
F’din il-marda, ġismek ma jkunx kapaċi jkisser kompletament
l-amino acid tyrosine (amino acids
huma blokok tal-bini tal-proteini tagħna), b’hekk jifforma sustanzi
ta’ ħsara. Dawn is-sustanzi
jakkumulaw f’ġismek. Nitisinone MDK
jimblokka t-tkissir ta’ tyrosine u s-sustanzi li jagħmlu l-ħsara
ma jiffurmawx.
Għandek issegwi dieta speċjali meta tkun qed tieħu din
il-mediċina, għax tyrosine jibqa’ f’ġismek. Din
id-dieta speċjali hija bbażata fuq kontenut baxx ta’ tyrosine u
ta’ phenylalanine (amino aċidu ieħor).
2.
X’GĦANDEK TKUN TAF QABEL MA TIEĦU NITISI
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
Prodott mediċinali li m’għadux awtorizzat
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Nitisinone MDK 2 mg kapsuli iebsin
Nitisinone MDK 5 mg kapsuli iebsin
Nitisinone MDK 10 mg kapsuli iebsin
Nitisinone MDK 20 mg kapsuli iebsin
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Nitisinone MDK 2 mg kapsuli iebsin
Kull kapsula iebsa fiha 2 mg ta’ nitisinone.
Nitisinone MDK 5
mg kapsuli iebsin
Kull kapsula iebsa fiha 5 mg ta’ nitisinone.
Nitisinone MDK 10 mg kapsuli iebsin
Kull kapsula iebsa fiha 10 mg ta’ nitisinone.
Nitisinone MDK 20
mg kapsuli iebsin
Kull kapsula iebsa fiha 20 mg ta’ nitisinone.
Għal-lista sħiħa ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Kapsula iebsa.
Il-kapsuli fihom trab abjad għal abjad mitfi.
Nitisinone MDK 2 mg kapsuli iebsin
Kapsuli bojod, opaki (15.7 mm), stampati b’linka sewda “2 mg”
fuq it-tapp u “Nitisinone” fuq il-parti
ta’ barra.
Nitisinone MDK 5
mg kapsuli iebsin
Kapsuli bojod, opaki (15.7 mm), stampati b’linka sewda “5 mg”
fuq it-tapp u “Nitisinone” fuq il-parti
ta’ barra.
Nitisinone MDK 10 mg kapsuli iebsin
Kapsuli bojod, opaki (15.7 mm), stampati b’linka sewda “10 mg”
fuq it-tapp u “Nitisinone” fuq il-
parti ta’ barra.
Nitisinone MDK 20
mg kapsuli iebsin
Kapsuli bojod, opaki (15.7 mm), stampati b’linka sewda “20 mg”
fuq it-tapp u “Nitisinone” fuq il-
parti ta’ barra.
Prodott mediċinali li m’għadux awtorizzat
3
4
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Kura ta’ pazjenti adulti u pedjatriċi (f’kull medda ta’ età)
b’dijanjożi kkonfermata ta’ tirosinemija
ereditarja ta’ tip 1 (HT-1) flimkien ma’ restrizzjoni tad-dieta
ta’ tyrosine u phenylalanine.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Il-kura b’nitisinone trid tinbeda u tiġi mmaniġġjata minn tabib
li għandu esperjenza fil-kura ta’
pazjenti bl-HT-1.
Pożoloġija
Il-kura tal-ġenotipi kollha tal-marda għandhom jinbdew kmieni kemm
jista’ jkun biex iżidu s-
sopravi
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 14-06-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 14-06-2023
Public Assessment Report Public Assessment Report Bulgarian 14-06-2023
Patient Information leaflet Patient Information leaflet Spanish 14-06-2023
Public Assessment Report Public Assessment Report Spanish 14-06-2023
Patient Information leaflet Patient Information leaflet Czech 14-06-2023
Public Assessment Report Public Assessment Report Czech 14-06-2023
Patient Information leaflet Patient Information leaflet Danish 14-06-2023
Public Assessment Report Public Assessment Report Danish 14-06-2023
Patient Information leaflet Patient Information leaflet German 14-06-2023
Public Assessment Report Public Assessment Report German 14-06-2023
Patient Information leaflet Patient Information leaflet Estonian 14-06-2023
Public Assessment Report Public Assessment Report Estonian 14-06-2023
Patient Information leaflet Patient Information leaflet Greek 14-06-2023
Public Assessment Report Public Assessment Report Greek 14-06-2023
Patient Information leaflet Patient Information leaflet English 14-06-2023
Public Assessment Report Public Assessment Report English 14-06-2023
Patient Information leaflet Patient Information leaflet French 14-06-2023
Public Assessment Report Public Assessment Report French 14-06-2023
Patient Information leaflet Patient Information leaflet Italian 14-06-2023
Public Assessment Report Public Assessment Report Italian 14-06-2023
Patient Information leaflet Patient Information leaflet Latvian 14-06-2023
Public Assessment Report Public Assessment Report Latvian 14-06-2023
Patient Information leaflet Patient Information leaflet Lithuanian 14-06-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 14-06-2023
Public Assessment Report Public Assessment Report Lithuanian 14-06-2023
Patient Information leaflet Patient Information leaflet Hungarian 14-06-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 14-06-2023
Public Assessment Report Public Assessment Report Hungarian 14-06-2023
Patient Information leaflet Patient Information leaflet Dutch 14-06-2023
Public Assessment Report Public Assessment Report Dutch 14-06-2023
Patient Information leaflet Patient Information leaflet Polish 14-06-2023
Public Assessment Report Public Assessment Report Polish 14-06-2023
Patient Information leaflet Patient Information leaflet Portuguese 14-06-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 14-06-2023
Public Assessment Report Public Assessment Report Portuguese 14-06-2023
Patient Information leaflet Patient Information leaflet Romanian 14-06-2023
Public Assessment Report Public Assessment Report Romanian 14-06-2023
Patient Information leaflet Patient Information leaflet Slovak 14-06-2023
Public Assessment Report Public Assessment Report Slovak 14-06-2023
Patient Information leaflet Patient Information leaflet Slovenian 14-06-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 14-06-2023
Public Assessment Report Public Assessment Report Slovenian 14-06-2023
Patient Information leaflet Patient Information leaflet Finnish 14-06-2023
Public Assessment Report Public Assessment Report Finnish 14-06-2023
Patient Information leaflet Patient Information leaflet Swedish 14-06-2023
Public Assessment Report Public Assessment Report Swedish 14-06-2023
Patient Information leaflet Patient Information leaflet Norwegian 14-06-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 14-06-2023
Patient Information leaflet Patient Information leaflet Icelandic 14-06-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 14-06-2023
Patient Information leaflet Patient Information leaflet Croatian 14-06-2023
Public Assessment Report Public Assessment Report Croatian 14-06-2023

Search alerts related to this product