Tukysa

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

Tucatinib

Available from:

Seagen B.V.

ATC code:

L01EH03

INN (International Name):

tucatinib

Therapeutic group:

Aġenti antineoplastiċi

Therapeutic area:

Breast Neoplasms; Neoplasm Metastasis

Therapeutic indications:

Tukysa is indicated in combination with trastuzumab and capecitabine for the treatment of adult patients with HER2‑positive locally advanced or metastatic breast cancer who have received at least 2 prior anti‑HER2 treatment regimens.

Product summary:

Revision: 5

Authorization status:

Awtorizzat

Authorization date:

2021-02-11

Patient Information leaflet

                                29
B. FULJETT TA’ TAGĦRIF_ _
30
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-PAZJENT
TUKYSA 50 MG PILLOLI MIKSIJA B’RITA
TUKYSA 150 MG PILLOLI MIKSIJA B’RITA
tucatinib
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 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 TUKYSA u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tieħu TUKYSA
3.
Kif għandek tieħu TUKYSA
4.
Effetti sekondarji possibbli
5.
Kif taħżen TUKYSA
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU TUKYSA U GĦALXIEX JINTUŻA
X’INHU TUKYSA
TUKYSA huwa mediċina għall-kanċer tas-sider. Dan fih is-sustanza
attiva tucatinib u jappartjeni għal
grupp ta’ mediċini msejħa inibituri ta’ protein kinase li
jipprevjenu t-tkabbir ta’ xi tipi ta’ ċelluli tal-
kanċer fil-ġisem.
GĦALXIEX JINTUŻA TUKYSA
TUKYSA jintuża għall-adulti li għandhom kanċer tas-sider li:
-
għandu riċettur (mira) fuq iċ-ċelluli tal-kanċer imsejħa
riċettur 2 tal-fattur tat-tkabbir epidermali
tal-bniedem (kanċer tas-sider pożittiv għall-HER2)
-
infirex lil hinn mit-tumur oriġinali jew għal organi oħra
bħall-moħħ jew ma jistax jitneħħa
b’k
                                
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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 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
TUKYSA 50 mg pilloli miksija b’rita
TUKYSA 150 mg pilloli miksija b’rita
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
TUKYSA 50 mg pilloli miksija b’rita
Kull pillola miksija b’rita fiha 50 mg ta’ tucatinib.
TUKYSA 150 mg pilloli miksija b’rita
Kull pillola miksija b’rita fiha 150 mg ta’ tucatinib.
Eċċipjenti b’effett magħruf
Kull pillola miksija b’rita ta’ 150 mg fiha 27.64 mg ta’ sodium
u 30.29 mg ta’ potassium.
Doża ta’ 300 mg ta’ TUKYSA fiha 55.3 mg ta’ sodium u 60.6 mg
ta’ potassium.
_ _
Għal-lista sħiħa ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Pillola miksija b’rita (pillola).
TUKYSA 50 mg pilloli miksija b’rita
Pillola miksija b’rita tonda u safra, li għandha “TUC” imnaqqax
fuq naħa waħda u “50” fuq in-naħa l-
oħra. Il-pillola ta’ 50 mg għandha dijametru ta’ madwar 8 mm.
TUKYSA 150 mg pilloli miksija b’rita
Pillola miksija b’rita ovali u safra, li għandha “TUC” imnaqqax
fuq naħa waħda u “150” fuq in-naħa l-
oħra. Il-pillola ta’ 150 mg hija twila madwar 17-il mm u wiesgħa 7
mm.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
TUKYSA huwa indikat flimkien ma’ trastuzumab u capecitabine
għat-trattament ta’ pazjenti adulti
b’kanċer tas-sider pożittiv għall-HER2 lokalment avvanzat jew
metastatiku li rċevew mill-inqas 2
korsijiet ta’ trattament kontra HER2 qabel.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
It-trattament b’TUKYSA għandu jinbeda u jkun sorveljat minn tabib
b’esperjenza fl-għoti ta’ prodotti
mediċinali kontra l-kanċer.
3
Pożoloġija
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 04-04-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 04-04-2024
Public Assessment Report Public Assessment Report Bulgarian 18-02-2021
Patient Information leaflet Patient Information leaflet Spanish 04-04-2024
Public Assessment Report Public Assessment Report Spanish 18-02-2021
Patient Information leaflet Patient Information leaflet Czech 04-04-2024
Public Assessment Report Public Assessment Report Czech 18-02-2021
Patient Information leaflet Patient Information leaflet Danish 04-04-2024
Public Assessment Report Public Assessment Report Danish 18-02-2021
Patient Information leaflet Patient Information leaflet German 04-04-2024
Public Assessment Report Public Assessment Report German 18-02-2021
Patient Information leaflet Patient Information leaflet Estonian 04-04-2024
Public Assessment Report Public Assessment Report Estonian 18-02-2021
Patient Information leaflet Patient Information leaflet Greek 04-04-2024
Public Assessment Report Public Assessment Report Greek 18-02-2021
Patient Information leaflet Patient Information leaflet English 04-04-2024
Public Assessment Report Public Assessment Report English 18-02-2021
Patient Information leaflet Patient Information leaflet French 04-04-2024
Public Assessment Report Public Assessment Report French 18-02-2021
Patient Information leaflet Patient Information leaflet Italian 04-04-2024
Public Assessment Report Public Assessment Report Italian 18-02-2021
Patient Information leaflet Patient Information leaflet Latvian 04-04-2024
Public Assessment Report Public Assessment Report Latvian 18-02-2021
Patient Information leaflet Patient Information leaflet Lithuanian 04-04-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 04-04-2024
Public Assessment Report Public Assessment Report Lithuanian 18-02-2021
Patient Information leaflet Patient Information leaflet Hungarian 04-04-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 04-04-2024
Public Assessment Report Public Assessment Report Hungarian 18-02-2021
Patient Information leaflet Patient Information leaflet Dutch 04-04-2024
Public Assessment Report Public Assessment Report Dutch 18-02-2021
Patient Information leaflet Patient Information leaflet Polish 04-04-2024
Public Assessment Report Public Assessment Report Polish 18-02-2021
Patient Information leaflet Patient Information leaflet Portuguese 04-04-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 04-04-2024
Public Assessment Report Public Assessment Report Portuguese 18-02-2021
Patient Information leaflet Patient Information leaflet Romanian 04-04-2024
Public Assessment Report Public Assessment Report Romanian 18-02-2021
Patient Information leaflet Patient Information leaflet Slovak 04-04-2024
Public Assessment Report Public Assessment Report Slovak 18-02-2021
Patient Information leaflet Patient Information leaflet Slovenian 04-04-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 04-04-2024
Public Assessment Report Public Assessment Report Slovenian 18-02-2021
Patient Information leaflet Patient Information leaflet Finnish 04-04-2024
Public Assessment Report Public Assessment Report Finnish 18-02-2021
Patient Information leaflet Patient Information leaflet Swedish 04-04-2024
Public Assessment Report Public Assessment Report Swedish 18-02-2021
Patient Information leaflet Patient Information leaflet Norwegian 04-04-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 04-04-2024
Patient Information leaflet Patient Information leaflet Icelandic 04-04-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 04-04-2024
Patient Information leaflet Patient Information leaflet Croatian 04-04-2024
Public Assessment Report Public Assessment Report Croatian 18-02-2021

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