Alunbrig

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

brigatinib

Available from:

Takeda Pharma A/S

ATC code:

L01XE43

INN (International Name):

brigatinib

Therapeutic group:

Aġenti antineoplastiċi

Therapeutic area:

Karċinoma, Pulmun Mhux taċ-Ċellula Żgħira

Therapeutic indications:

Alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase (ALK)‑positive advanced non‑small cell lung cancer (NSCLC) previously not treated with an ALK inhibitor. Alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase ALKpositive advanced NSCLC previously treated with crizotinib.

Product summary:

Revision: 9

Authorization status:

Awtorizzat

Authorization date:

2018-11-22

Patient Information leaflet

                                59
B. FULJETT TA
’
TAGĦRIF
60
FULJETT TA
’
TAGĦRIF: INFORMAZZJONI GĦALL-PAZJENT
ALUNBRIG 30 MG PILLOLI MIKSIJA B
’
RITA
ALUNBRIG 90 MG PILLOLI MIKSIJA B
’
RITA
ALUNBRIG 180 MG
PILLOLI MIKSIJA B
’
RITA
brigatinib
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 sezzjoni 4.
F
’
DAN IL-FULJETT
1.
X
’
inhu Alunbrig u għalxiex jintuża
2.
X
’
għandek tkun taf qabel ma tieħu Alunbrig
3.
Kif għandek tieħu Alunbrig
4.
Effetti sekondarji possibbli
5.
Kif taħżen Alunbrig
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X
’
INHU ALUNBRIG U GĦALXIEX JINTUŻA
Alunbrig fih is-sustanza attiva brigatinib, tip ta’ mediċina kontra
l-kanċer li tissejjaħ inibitur
tal-kinase. Alunbrig jintuża biex jittratta adulti bi stadju avvanzat
ta
’
KANĊER TAL-PULMUN
li jissejjaħ
kanċer tal-pulmun ta
’
ċelluli mhux żgħar. Jingħata lil pazjenti li għandhom il-kanċer
tal-pulmun
tagħhom relatat ma’ forma ta’ ġene mhux normali li tissejjaħ
kinase limfoma anaplastika (ALK,
_anaplastic lymphoma kinase_
).
KIF JAĦDEM ALUNBRIG
Il-ġene mhux normali tipproduċi proteina magħrufa bħala kinase li
tistimula l-iżvilupp taċ-ċelluli
tal-kanċer. Alunbrig jimblokka l-azzjoni ta
’
din il-proteina anormali u b
’
hekk inaqqas ir-rata
tat-tkabbir u l-firxa tal-kanċer.
2.
X
’
GĦANDEK TKUN TAF QABEL MA TIEĦU ALUNBRIG
_ _
TIĦUX ALUNBRIG
•
jekk inti
ALLERĠIKU
għal brigatinib jew għal xi sustanza oħra ta
’
din il-mediċina (imn
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Alunbrig 30 mg pilloli miksija b
’
rita
Alunbrig 90 mg pilloli miksija b
’
rita
Alunbrig 180 mg pilloli miksija b
’
rita
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Alunbrig 30 mg pilloli miksija b
’
rita
Kull pillola miksija b
’
rita fiha 30 mg ta
’
brigatinib.
_Eċċipjent b_
’
_effett magħruf _
Kull pillola miksija b
’
rita fiha 56 mg ta
’
lactose monohydrate.
Alunbrig 90 mg pilloli miksija b
’
rita
Kull pillola miksija fiha 90 mg ta
’
brigatinib.
_Eċċipjent b_
’
_effett magħruf _
Kull pillola miksija b
’
rita fiha 168 mg ta
’
lactose monohydrate.
Alunbrig 180 mg pilloli miksija b
’
rita
Kull pillola miksija b
’
rita fiha 180 mg ta
’
brigatinib.
_Eċċipjent b_
’
_effett magħruf _
Kull pillola miksija b
’
rita fiha 336 mg ta
’
lactose monohydrate.
Għal-lista sħiħa ta
’
eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Pillola miksija b
’
rita (pillola)
Alunbrig 30 mg pilloli miksija b
’
rita
Pillola miksija b
’
rita tonda, bajda għal kważi bajda b
’
dijametru ta
’
madwar 7 mm imnaqqxa b
“’
U3
”
fuq naħa waħda u xejn fuq in-naħa l-oħra.
Alunbrig 90 mg pilloli miksija b
’
rita
Pillola miksija b
’
rita ovali, bajda għal kważi bajda b
’
tul ta
’
madwar 15 mm imnaqqxa b
“’
U7
”
fuq naħa
waħda u xejn fuq in-naħa l-oħra.
Alunbrig 180 mg pilloli miksija b
’
rita
Pillola miksija b
’
rita ovali, bajda għal kważi bajda b
’
tul ta
’
madwar 19 mm imnaqqxa b
“’
U13
”
fuq
naħa waħda u xejn fuq in-naħa l-oħra.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Alunbrig huwa indikat bħala monoterapija għat-trattament ta’
pazjenti adulti b’kanċer avvanzat
tal-pulmun ta’ ċelluli mhux żgħar (NSCLC,
_non-small cell lung cancer_
) pożittiv għal kinase
3
anaplastika tal-limfoma (ALK,
_anaplastic lymphoma kinase_
) li qatt ma ġew ittrattati b’inibitur ta’
ALK.
Alunbrig huwa indikat bħala monoterapija għat-trattame
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 22-09-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 22-09-2023
Public Assessment Report Public Assessment Report Bulgarian 11-06-2020
Patient Information leaflet Patient Information leaflet Spanish 22-09-2023
Public Assessment Report Public Assessment Report Spanish 11-06-2020
Patient Information leaflet Patient Information leaflet Czech 22-09-2023
Public Assessment Report Public Assessment Report Czech 11-06-2020
Patient Information leaflet Patient Information leaflet Danish 22-09-2023
Public Assessment Report Public Assessment Report Danish 11-06-2020
Patient Information leaflet Patient Information leaflet German 22-09-2023
Public Assessment Report Public Assessment Report German 11-06-2020
Patient Information leaflet Patient Information leaflet Estonian 22-09-2023
Public Assessment Report Public Assessment Report Estonian 11-06-2020
Patient Information leaflet Patient Information leaflet Greek 22-09-2023
Public Assessment Report Public Assessment Report Greek 11-06-2020
Patient Information leaflet Patient Information leaflet English 22-09-2023
Public Assessment Report Public Assessment Report English 11-06-2020
Patient Information leaflet Patient Information leaflet French 22-09-2023
Public Assessment Report Public Assessment Report French 11-06-2020
Patient Information leaflet Patient Information leaflet Italian 22-09-2023
Public Assessment Report Public Assessment Report Italian 11-06-2020
Patient Information leaflet Patient Information leaflet Latvian 22-09-2023
Public Assessment Report Public Assessment Report Latvian 11-06-2020
Patient Information leaflet Patient Information leaflet Lithuanian 22-09-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 22-09-2023
Public Assessment Report Public Assessment Report Lithuanian 11-06-2020
Patient Information leaflet Patient Information leaflet Hungarian 22-09-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 22-09-2023
Public Assessment Report Public Assessment Report Hungarian 11-06-2020
Patient Information leaflet Patient Information leaflet Dutch 22-09-2023
Public Assessment Report Public Assessment Report Dutch 11-06-2020
Patient Information leaflet Patient Information leaflet Polish 22-09-2023
Public Assessment Report Public Assessment Report Polish 11-06-2020
Patient Information leaflet Patient Information leaflet Portuguese 22-09-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 22-09-2023
Public Assessment Report Public Assessment Report Portuguese 11-06-2020
Patient Information leaflet Patient Information leaflet Romanian 22-09-2023
Public Assessment Report Public Assessment Report Romanian 11-06-2020
Patient Information leaflet Patient Information leaflet Slovak 22-09-2023
Public Assessment Report Public Assessment Report Slovak 11-06-2020
Patient Information leaflet Patient Information leaflet Slovenian 22-09-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 22-09-2023
Public Assessment Report Public Assessment Report Slovenian 11-06-2020
Patient Information leaflet Patient Information leaflet Finnish 22-09-2023
Public Assessment Report Public Assessment Report Finnish 11-06-2020
Patient Information leaflet Patient Information leaflet Swedish 22-09-2023
Public Assessment Report Public Assessment Report Swedish 11-06-2020
Patient Information leaflet Patient Information leaflet Norwegian 22-09-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 22-09-2023
Patient Information leaflet Patient Information leaflet Icelandic 22-09-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 22-09-2023
Patient Information leaflet Patient Information leaflet Croatian 22-09-2023
Public Assessment Report Public Assessment Report Croatian 11-06-2020

Search alerts related to this product

View documents history