Bortezomib Fresenius Kabi

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

bortezomib

Available from:

Fresenius Kabi Deutschland GmbH

ATC code:

L01XG01

INN (International Name):

bortezomib

Therapeutic group:

Aġenti antineoplastiċi

Therapeutic area:

Majloma Multipla

Therapeutic indications:

Bortezomib bħala monoterapija jew flimkien ma 'liposomal doxorubicin jew dexamethasone hu indikat għall-kura ta' pazjenti adulti b'progressiva majeloma multipla li rċevew mill-anqas terapija 1 minn qabel u li diġà għaddew jew li mhumiex tajbin għal trapjant b ' ċelluli staminali ematopojetiċi. Bortezomib flimkien ma 'melphalan u prednisone huwa indikat għall-kura ta' pazjenti adulti li ma kienux ikkurati qabel mjeloma multipla li mhumiex eliġibbli għal doża għolja ta 'kimoterapija bi trapjant b' ċelluli staminali ematopojetiċi. Bortezomib flimkien ma 'dexamethasone, jew ma' dexamethasone u thalidomide, huwa indikat għall-kura ta 'induzzjoni ta' pazjenti adulti li ma kienux ikkurati qabel mjeloma multipla li huma eliġibbli għal doża għolja ta 'kimoterapija bi trapjant b' ċelluli staminali ematopojetiċi. Bortezomib flimkien ma 'rituximab, cyclophosphamide, doxorubicin u prednisone huwa indikat għall-kura ta' pazjenti adulti li ma kienux ikkurati qabel f'forma ta'tubu taċ-ċelluli tal-limfoma li mhumiex tajbin għal trapjant b ' ċelluli staminali ematopojetiċi.

Product summary:

Revision: 5

Authorization status:

Awtorizzat

Authorization date:

2019-11-14

Patient Information leaflet

                                84
B. FULJETT TA’ TAGĦRIF
85
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦAL MIN QED JAGĦMEL UŻU
MINNU
BORTEZOMIB FRESENIUS KABI 1 MG TRAB GĦAL SOLUZZJONI GĦALL-INJEZZJONI
bortezomib
AQRA SEW DAN IL-FULJETT KOLLU QABEL TIBDA TUŻA 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.
-
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 Bortezomib Fresenius Kabi u għal xiex jintuża
2.
Xgħandek tkun taf qabel ma tuża Bortezomib Fresenius Kabi
3.
Kif għandek tuża Bortezomib Fresenius Kabi
4.
Effetti sekondarji possibbli
5.
Kif taħżen Bortezomib Fresenius Kabi
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU BORTEZOMIB FRESENIUS KABI U GĦAL XIEX JINTUŻA
Din il-mediċina fiha s-sustanza attiva bortezomib, hekk imsejjaħ
‘impeditur ta’ proteasome’.
Il-proteasomes għandhom rwol important fil-kontroll tal-funzjoni u
t-tkabbir taċ-ċellula. Billi
jinterferixxi mal-funzjoni tagħhom, bortezomib jista’ joqtol
iċ-ċelluli tal-kanċer.
Bortezomib jintuża għat-trattament ta’ majeloma multipla (kanċer
tal-mudullun) f’pazjenti li diġà
għalqu it-18-il sena:
-
waħdu jew flimkien mal-mediċini pegylated liposomal doxorubicin jew
dexamethasone għal
pazjenti li l-marda tagħhom qed tiħrax (progressiva) wara li jkunu
rċivew mill-anqas trattament
ieħor qabel u li għalihom trapjant b’ċelluli steminali tad-demm
ma kienx irnexxa fihom jew
mhuwiex tajjeb għalihom.
-
flimkien mal-mediċini melphalan u prednisone, għal pazjenti li
l-marda tagħhom qatt ma ġietx
ittrattata qabel u li mhumiex eliġibbli għal doża għolja ta’
kimoterapija ma’ trapjant ta’ ċelluli
steminali tad-demm.
-
flimkien mal-mediċini oħra dexamethasone jew dexamethasone flimkien
ma’thalidomide
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Bortezomib Fresenius Kabi 1 mg trab għal soluzzjoni għall-injezzjoni
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Kull kunjett fih 1 mg ta’ bortezomib (bħala mannitol boronic
ester).
Wara li jiġi rrikostitwit, 1 ml tas-soluzzjoni għall-injezzjoni
ġol-vina jkun fih 1 mg bortezomib
Għal-lista sħiħa ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Trab għal soluzzjoni għall-injezzjoni.
Trab lijofilizzat jew kejk minn abjad sa offwajt.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Bortezomib huwa indikat biex jingħata bħala trattament waħdu jew
f’kombinazzjoni ma’ pegylated
liposomal doxorubicin jew dexamethasome għal pazjenti adulti
b’majeloma multipla progressiva li
ngħataw mill-inqas terapija waħda qabel u li diġà kellhom jew mhux
eliġibbli għal trapjant ta’ ċelluli
steminali ematopojetiċi.
Bortezomib flimkien ma’ melphalan u prednisone huwa indikat
għat-trattament ta’ pazjenti adulti
b’majeloma multipla li qatt ma kienet ittrattata qabel li mhumiex
eleġibbli għal doża għolja ta’
kimoterapija bi trapjant ta’ ċelluli steminali ematopojetiċi.
Bortezomib flimkien ma’ dexamethasone, jew b’dexamethasone u
thalidomide, huwa indikat għat-
trattament ta’ pazjenti adulti b’majeloma multipla li qatt ma
kienet ittrattata qabel u li mhumiex
eleġibbli għal doża għolja ta’ kimoterapija bi trapjant ta’
ċelluli steminali ematopojetiċi.
Bortezomib flimkien ma’ rituximab, cyclophosphamide, doxorubicin u
prednisone huwa indikat għat-
trattament ta’ pazjenti adulti b’limfoma taċ-ċellula mantle li
qatt ma kienet ittrattata qabel li mhumiex
addattati għal trapjant taċ-ċellula steminali ematopojetika.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
It-trattament bi bortezomib għandu jinbeda taħt is-superviżjoni
ta’ tabib b’esperjenza fit-trattament ta’
pazjenti bil-kanċer, madankollu bortezomib jista’ jingħata minn
professjonist fil-qasam
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 07-02-2024
Public Assessment Report Public Assessment Report Bulgarian 25-11-2019
Patient Information leaflet Patient Information leaflet Spanish 07-02-2024
Public Assessment Report Public Assessment Report Spanish 25-11-2019
Patient Information leaflet Patient Information leaflet Czech 07-02-2024
Public Assessment Report Public Assessment Report Czech 25-11-2019
Patient Information leaflet Patient Information leaflet Danish 07-02-2024
Public Assessment Report Public Assessment Report Danish 25-11-2019
Patient Information leaflet Patient Information leaflet German 07-02-2024
Public Assessment Report Public Assessment Report German 25-11-2019
Patient Information leaflet Patient Information leaflet Estonian 07-02-2024
Public Assessment Report Public Assessment Report Estonian 25-11-2019
Patient Information leaflet Patient Information leaflet Greek 07-02-2024
Public Assessment Report Public Assessment Report Greek 25-11-2019
Patient Information leaflet Patient Information leaflet English 07-02-2024
Public Assessment Report Public Assessment Report English 25-11-2019
Patient Information leaflet Patient Information leaflet French 07-02-2024
Public Assessment Report Public Assessment Report French 25-11-2019
Patient Information leaflet Patient Information leaflet Italian 07-02-2024
Public Assessment Report Public Assessment Report Italian 25-11-2019
Patient Information leaflet Patient Information leaflet Latvian 07-02-2024
Public Assessment Report Public Assessment Report Latvian 25-11-2019
Patient Information leaflet Patient Information leaflet Lithuanian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 07-02-2024
Public Assessment Report Public Assessment Report Lithuanian 25-11-2019
Patient Information leaflet Patient Information leaflet Hungarian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 07-02-2024
Public Assessment Report Public Assessment Report Hungarian 25-11-2019
Patient Information leaflet Patient Information leaflet Dutch 07-02-2024
Public Assessment Report Public Assessment Report Dutch 25-11-2019
Patient Information leaflet Patient Information leaflet Polish 07-02-2024
Public Assessment Report Public Assessment Report Polish 25-11-2019
Patient Information leaflet Patient Information leaflet Portuguese 07-02-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 07-02-2024
Public Assessment Report Public Assessment Report Portuguese 25-11-2019
Patient Information leaflet Patient Information leaflet Romanian 07-02-2024
Public Assessment Report Public Assessment Report Romanian 25-11-2019
Patient Information leaflet Patient Information leaflet Slovak 07-02-2024
Public Assessment Report Public Assessment Report Slovak 25-11-2019
Patient Information leaflet Patient Information leaflet Slovenian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 07-02-2024
Public Assessment Report Public Assessment Report Slovenian 25-11-2019
Patient Information leaflet Patient Information leaflet Finnish 07-02-2024
Public Assessment Report Public Assessment Report Finnish 25-11-2019
Patient Information leaflet Patient Information leaflet Swedish 07-02-2024
Public Assessment Report Public Assessment Report Swedish 25-11-2019
Patient Information leaflet Patient Information leaflet Norwegian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 07-02-2024
Patient Information leaflet Patient Information leaflet Icelandic 07-02-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 07-02-2024
Patient Information leaflet Patient Information leaflet Croatian 07-02-2024
Public Assessment Report Public Assessment Report Croatian 25-11-2019

Search alerts related to this product