Myocet liposomal (previously Myocet)

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

doxorubicin hydrochloride

Available from:

Teva B.V.

ATC code:

L01DB01

INN (International Name):

doxorubicin

Therapeutic group:

Aġenti antineoplastiċi

Therapeutic area:

Neoplażmi tas-Sider

Therapeutic indications:

Myocet doxorubicin, f'kombinazzjoni ma 'cyclophosphamide, huwa indikat għall-kura preferita ta' kanċer metastatiku tas-sider f'nisa adulti.

Product summary:

Revision: 24

Authorization status:

Awtorizzat

Authorization date:

2000-07-13

Patient Information leaflet

                                31
B. FULJETT TA’ TAGĦRIF
32
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-UTENT
MYOCET LIPOSOMAL 50 MG TRAB, TIXRID U SOLVENT GĦAL KONĊENTRAT
GĦAT-TIXRID GĦALL-INFUŻJONI
Liposomali doxorubicin hydrochloride
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, 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-infermier
tiegħek. Dan jinkludi xi effett
sekondarju possibbli li mhuwiex elenkat f’dan il-fuljett. Ara
sezzjoni 4.
F’DAN IL-FULJETT
1.
X’inhu Myocet liposomal u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tieħu Myocet liposomal
3.
Kif għandu jingħata Myocet liposomal
4.
Effetti sekondarji possibbli
5.
Kif taħżen Myocet liposomal
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU MYOCET LIPOSOMAL U GĦALXIEX JINTUŻA
Myocet liposomal fih a mediċina msejħa “doxorubicin”, li
tagħmel ħsara liċ-ċelluli tat-tumur. Din it-
tip ta’ mediċina hi msejħa “kimoterapija”. Il-mediċina tinsab
ġo qtar żgħir ħafna ta’ xaħam imsejjaħ
“liposomi”.
Myocet liposomal jintuża f’nisa adulti għall-kura primarja ta’
kanċer tas-sider li jkun infirex (“kanċer
metastatiku tas-sider”). Jintuża ma’ mediċina oħra msejħa
“cyclophosphamide”. Jekk jogħġbok aqra
wkoll b’attenzjoni l-fuljett ta’ tagħrif għall-pazjent li jiġi
ma’ dik il-mediċina.
2.
X'GĦANDEK TKUN TAF QABEL MA TIEĦU MYOCET LIPOSOMAL
TIĦUX MYOCET LIPOSOMAL:
•
jekk inti allerġiku għal doxorubicin jew għal xi sustanza oħra
ta’ din il-mediċina (imniżżla fis-
sezzjoni 6).
M’għandekx tirċievi Myocet liposomal jekk dan japplika għalik.
Jekk m’intix ċert
                                
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Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Myocet liposomal 50 mg trab, tixrid u solvent għal konċentrat
għat-tixrid għall-infużjoni
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Kumpless ta’ doxorubicin-citrate enkapsulat f’liposoma li
jikkorispondi għal 50 mg doxorubicin
hydrochloride (HCl).
Eċċipjent(i) b’effett magħruf: Il-prodott mediċinali rikostitwit
fih madwar 108 mg ta’ sodium għal
doża ta’ 50 mg ta’ doxorubicin HCl.
Għal-lista sħiħa ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Trab, tixrid u solvent għal konċentrat għat-tixrid
għall-infużjoni.
Myocet liposomal huwa provdut bħala sistema bi 3 kunjetti kif ġej:
Kunjett 1 - doxorubicin HCl hu trab aħmar lajofilizzat.
Kunjett 2 - liposomi hi tixrid bajda tagħti fl-offwajt, opaka u
omoġena.
Kunjett 3 - baffer hu soluzzjoni ċara ta’ bla kulur.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Myocet liposomal, flimkien ma’ cyclophosphamide, huwa intiż bħala
l-ewwel fazi fil-kura ta’ kanċer
tas-sider fl-istadju metastatiku f’nisa adulti.
_ _
_ _
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Myocet liposomal għandu jingħata biss f’entitajiet li huma
speċjalizzati fl-għoti ta’ kemjoterapija
ċitotossika, u għandu jingħata biss taħt superviżjoni ta’ tabib
b’experjenza fl-użu ta’ kemjoterapija.
Pożoloġija
Meta Myocet liposomal jiġi mogħti flimkien ma’ cyclophosphamide
(600 mg/m
2
) d-doża inizjali
rakkomandata ta’ Myocet liposomal hi ta’ 60-75 mg/m
2
darba kull tlett ġimgħat.
_Persuni akbar fl-età_
Is-sigurtà u l-effikaċja ta’ Myocet liposomal ġew studjati f’61
pazjent li kellhom 65 sena jew aktar,
b’kanċer fis-sider fl-istadju metastatiku. Informazzjoni miġbura
minn
_randomised controlled clinical _
_trtials_
turi li l-effikaċja u s-sigurtà kardijaka ta’ Myocet liposomal
f’din il-popolazzjoni kienu
paragunabbli ma’ dawk osservati f’pazjenti li għandhom inqas minn
65 sena.
_Pazjenti b’indebolime
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 24-03-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 24-03-2023
Public Assessment Report Public Assessment Report Bulgarian 04-02-2020
Patient Information leaflet Patient Information leaflet Spanish 24-03-2023
Public Assessment Report Public Assessment Report Spanish 04-02-2020
Patient Information leaflet Patient Information leaflet Czech 24-03-2023
Public Assessment Report Public Assessment Report Czech 04-02-2020
Patient Information leaflet Patient Information leaflet Danish 24-03-2023
Public Assessment Report Public Assessment Report Danish 04-02-2020
Patient Information leaflet Patient Information leaflet German 24-03-2023
Public Assessment Report Public Assessment Report German 04-02-2020
Patient Information leaflet Patient Information leaflet Estonian 24-03-2023
Public Assessment Report Public Assessment Report Estonian 04-02-2020
Patient Information leaflet Patient Information leaflet Greek 24-03-2023
Public Assessment Report Public Assessment Report Greek 04-02-2020
Patient Information leaflet Patient Information leaflet English 24-03-2023
Public Assessment Report Public Assessment Report English 04-02-2020
Patient Information leaflet Patient Information leaflet French 24-03-2023
Public Assessment Report Public Assessment Report French 04-02-2020
Patient Information leaflet Patient Information leaflet Italian 24-03-2023
Public Assessment Report Public Assessment Report Italian 04-02-2020
Patient Information leaflet Patient Information leaflet Latvian 24-03-2023
Public Assessment Report Public Assessment Report Latvian 04-02-2020
Patient Information leaflet Patient Information leaflet Lithuanian 24-03-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 24-03-2023
Public Assessment Report Public Assessment Report Lithuanian 04-02-2020
Patient Information leaflet Patient Information leaflet Hungarian 24-03-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 24-03-2023
Public Assessment Report Public Assessment Report Hungarian 04-02-2020
Patient Information leaflet Patient Information leaflet Dutch 24-03-2023
Public Assessment Report Public Assessment Report Dutch 04-02-2020
Patient Information leaflet Patient Information leaflet Polish 24-03-2023
Public Assessment Report Public Assessment Report Polish 04-02-2020
Patient Information leaflet Patient Information leaflet Portuguese 24-03-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 24-03-2023
Public Assessment Report Public Assessment Report Portuguese 04-02-2020
Patient Information leaflet Patient Information leaflet Romanian 24-03-2023
Public Assessment Report Public Assessment Report Romanian 04-02-2020
Patient Information leaflet Patient Information leaflet Slovak 24-03-2023
Public Assessment Report Public Assessment Report Slovak 04-02-2020
Patient Information leaflet Patient Information leaflet Slovenian 24-03-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 24-03-2023
Public Assessment Report Public Assessment Report Slovenian 04-02-2020
Patient Information leaflet Patient Information leaflet Finnish 24-03-2023
Public Assessment Report Public Assessment Report Finnish 04-02-2020
Patient Information leaflet Patient Information leaflet Swedish 24-03-2023
Public Assessment Report Public Assessment Report Swedish 04-02-2020
Patient Information leaflet Patient Information leaflet Norwegian 24-03-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 24-03-2023
Patient Information leaflet Patient Information leaflet Icelandic 24-03-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 24-03-2023
Patient Information leaflet Patient Information leaflet Croatian 24-03-2023
Public Assessment Report Public Assessment Report Croatian 04-02-2020

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