Lumark

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

lutetium (177Lu) chloride

Available from:

I.D.B. Radiopharmacy B.V.

ATC code:

V10

INN (International Name):

lutetium (177 Lu) chloride

Therapeutic group:

Radjofarmaċewtiċi terapewtiċi

Therapeutic area:

Radjonuklidi Imaging

Therapeutic indications:

Lumark huwa prekursur radjofarmaċewtiku. Mhuwiex maħsub għal użu dirett f'pazjenti. Din il-mediċina għandha tintuża biss għar-radjutikkettar ta 'molekuli ta' carrier, li ġew żviluppati u awtorizzati speċifikament għal radjutikkettar ma 'dan ir-radjonuklide.

Product summary:

Revision: 9

Authorization status:

Awtorizzat

Authorization date:

2015-06-18

Patient Information leaflet

                                21
B.
FULJETT TA’ TAGĦRIF
22
FULJETT TA' TAGĦRIF:
INFORMAZZJONI GĦALL-PAZJENT
LUMARK 80 GBQ/ML SOLUZZJONI TA’ PREKURSUR RADJUFARMAĊEWTIKU
Klorur tal-Lutezju (
177
Lu)
AQRA SEW DAN IL-FULJETT KOLLU QABEL TIBDA TINGĦATA L-MEDIĊINA
KKUMBINATA MA’ LUMARK PERESS LI FIH
INFORMAZZJONI IMPORTANTI GĦALIK.
-
Żomm dan il-fuljett. Jista’ jkollok bżonn terġa taqrah.
-
Jekk ikollok aktar mistoqsijiet, staqsi lit-tabib tal-mediċina
nukleari tiegħek li jkun qed jissorvelja l-
proċedura.
-
Jekk ikollok xi effett sekondarju kellem lit-tabib tal-mediċina
nukleari tiegħek. Dan jinkludi xi effett
sekondarju possibbli li mhuwiex elenkat f’dan il-fuljett. Ara
s-sezzjoni 4.
F'DAN IL-FULJETT
1.
X’inhu Lumark u għal xiex jintuża
2.
X’għandek tkun taf qabel ma tuża l-mediċina radjutikkettata
b’Lumark
3.
Kif għandek tuża mediċina radjutikkettata b’Lumark
4.
Effetti sekondarji possibbli
5.
Kif taħżen Lumark
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU LUMARK U GĦAL XIEX JINTUŻA
Lumark mhuwiex mediċina u mhuwiex maħsub li jintuża waħdu.
Lumark huwa imsejjaħ prekursur radjufarmaċewtiku. Fih is-sustanza
attiva klorur tal-lutezju (
177
Lu).
Lumark jintuża għar-radjutikkettar ta’ mediċini, teknika li biha
mediċini jiġu mmarkati (radjutikkettati)
b’forma radjuattiva tal-element Lutezju, magħruf bħala Lutezju (
177
Lu). Dawn il-mediċini imbagħad jistgħu
jintużaw fi proċeduri mediċi biex iġorru r-radjuattività sa fejn
hija meħtieġa fil-ġisem bħal siti ta’ ċelloli ta’
tumur.
Lumark jintuża biss biex jiġu radjutikkettati mediċini li ġew
żviluppati speċifikament għall-użu mas-sustanza
attiva klorur tal-Lutezju (
177
Lu).
L-użu ta’ mediċini tikkettati b’lutezju (
177
Lu) jinvolvi esponiment għal ammonti żgħar ta’ radjuattività.
It-
tabib tiegħek u t-tabib tal-mediċina nukleari tiegħek kkunsidraw li
l-benefiċċju kliniku li inti tikseb mill-
proċedura bil-prodott radjufarmaċewtiku huwa akbar mir-riskju
tar-radjazzjoni.
Jekk jogħġbok irr
                                
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Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM TAL-PRODOTT MEDIĊINALI
Lumark 80 GBq/mL prekursur radjufarmaċewtiku, soluzzjoni
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Kull mL wieħed ta’ soluzzjoni fih 80 GBq ta’ klorur tal-lutezju (
177
Lu) f’ħin ta’ referenza tal-attività (ART -
activity reference time), li jikkorrispondi bħala massimu għal
massimu ta' 160 mikrogramma ta’ lutezju. L-
ART huwa definit bħala t-tmiem tal-produzzjoni.
Kull kunjett fih volum li jvarja minn 0.1 sa 5 mL li jikkorrespondi
ma’ attività li tvarja minn 8 sa 400 GBq
(f’ART)
L-attività speċifika minima hija 500 GBq/mg ta’ lutezju (
177
Lu) f’ART.
Lutezju (
177
Lu) għandu semiħajja (half-life) ta’ 6.647 jiem. Lutezju (
177
Lu) jiġi prodott minn irradjazzjoni ta’
newtroni ta' lutezju (
176
Lu) arrikkit. Lutezju (
177
Lu) jiddekomponi b’emissjonijiet
-
β għal Hafnium (
177
Hf)
stabbli, bl-iktar β
-
abbundanti (79.3%) jkollu enerġija massima ta’ 0.497 MeV. Enerġija
gamma baxxa hija
wkoll emessa, pereżempju f’113 keV (6.2%) u 208 keV (11%).
Għal-lista sħiħa tal-eċċipjenti, ara s-sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Prekursur radjufarmaċewtiku, soluzzjoni.
Soluzzjoni ċara, mingħajr kulur
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Lumark huwa prekursur radjufarmaċewtiku. Mhuwiex maħsub għall-użu
dirett fil-pazjenti. Dan għandu
jintuża biss għar-radjutikkettar ta’ molekuli trasportaturi, li
jkunu ġew żviluppati apposta u awtorizzati għar-
radjutikkettar b’dan ir-radjunuklid.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Lumark għandu jintuża biss minn speċjalisti b’esperjenza
fir-radjutikkettar
_in vitro_
.
Pożoloġija
Il-kwantità
ta’
Lumark
meħtieġ
għal
radjutikkettar
u
l-kwantità
tal-prodott
mediċinali
li
għandu
jiġi
radjutikkettat
b’lutezju(
177
Lu)
li
tingħata
wara
jiddependu
fuq
il-prodott
mediċinali
li
għandu
jiġi
radjutikkettat u l-użu intiż tiegħu. Irreferi għas-Sommarju
tal-Karatteristiċi tal-Prodott/il-fuljet
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 29-09-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 29-09-2020
Public Assessment Report Public Assessment Report Bulgarian 14-01-2019
Patient Information leaflet Patient Information leaflet Spanish 29-09-2020
Public Assessment Report Public Assessment Report Spanish 14-01-2019
Patient Information leaflet Patient Information leaflet Czech 29-09-2020
Public Assessment Report Public Assessment Report Czech 14-01-2019
Patient Information leaflet Patient Information leaflet Danish 29-09-2020
Public Assessment Report Public Assessment Report Danish 14-01-2019
Patient Information leaflet Patient Information leaflet German 29-09-2020
Public Assessment Report Public Assessment Report German 14-01-2019
Patient Information leaflet Patient Information leaflet Estonian 29-09-2020
Public Assessment Report Public Assessment Report Estonian 14-01-2019
Patient Information leaflet Patient Information leaflet Greek 29-09-2020
Public Assessment Report Public Assessment Report Greek 14-01-2019
Patient Information leaflet Patient Information leaflet English 29-09-2020
Public Assessment Report Public Assessment Report English 14-01-2019
Patient Information leaflet Patient Information leaflet French 29-09-2020
Public Assessment Report Public Assessment Report French 14-01-2019
Patient Information leaflet Patient Information leaflet Italian 29-09-2020
Public Assessment Report Public Assessment Report Italian 14-01-2019
Patient Information leaflet Patient Information leaflet Latvian 29-09-2020
Public Assessment Report Public Assessment Report Latvian 14-01-2019
Patient Information leaflet Patient Information leaflet Lithuanian 29-09-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 29-09-2020
Public Assessment Report Public Assessment Report Lithuanian 14-01-2019
Patient Information leaflet Patient Information leaflet Hungarian 29-09-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 29-09-2020
Public Assessment Report Public Assessment Report Hungarian 14-01-2019
Patient Information leaflet Patient Information leaflet Dutch 29-09-2020
Public Assessment Report Public Assessment Report Dutch 14-01-2019
Patient Information leaflet Patient Information leaflet Polish 29-09-2020
Public Assessment Report Public Assessment Report Polish 14-01-2019
Patient Information leaflet Patient Information leaflet Portuguese 29-09-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 29-09-2020
Public Assessment Report Public Assessment Report Portuguese 14-01-2019
Patient Information leaflet Patient Information leaflet Romanian 29-09-2020
Public Assessment Report Public Assessment Report Romanian 14-01-2019
Patient Information leaflet Patient Information leaflet Slovak 29-09-2020
Public Assessment Report Public Assessment Report Slovak 14-01-2019
Patient Information leaflet Patient Information leaflet Slovenian 29-09-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 29-09-2020
Public Assessment Report Public Assessment Report Slovenian 14-01-2019
Patient Information leaflet Patient Information leaflet Finnish 29-09-2020
Public Assessment Report Public Assessment Report Finnish 14-01-2019
Patient Information leaflet Patient Information leaflet Swedish 29-09-2020
Public Assessment Report Public Assessment Report Swedish 14-01-2019
Patient Information leaflet Patient Information leaflet Norwegian 29-09-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 29-09-2020
Patient Information leaflet Patient Information leaflet Icelandic 29-09-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 29-09-2020
Patient Information leaflet Patient Information leaflet Croatian 29-09-2020
Public Assessment Report Public Assessment Report Croatian 14-01-2019

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