Lacosamide UCB

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

lacosamide

Available from:

UCB Pharma S.A.

ATC code:

N03AX18

INN (International Name):

lacosamide

Therapeutic group:

Anti-epilettiċi,

Therapeutic area:

Epilettiji, Parzjali

Therapeutic indications:

Lacosamide UCB huwa indikat bħala monoterapija u terapija aġġuntiva fil-kura ta 'aċċessjonijiet ta' bidu parzjali bi jew mingħajr ġeneralizzazzjoni sekondarja f'adulti, adolexxenti u tfal minn 4 snin b'epilessija.

Product summary:

Revision: 6

Authorization status:

Awtorizzat

Authorization date:

2019-08-26

Patient Information leaflet

                                125
B. FULJETT TA’ TAGĦRIF
126
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦAL PAZJENT
LACOSAMIDE UCB 50 MG PILLOLI MIKSIJA B’RITA
LACOSAMIDE UCB 100 MG PILLOLI MIKSIJA B’RITA
LACOSAMIDE UCB 150 MG PILLOLI MIKSIJA B’RITA
LACOSAMIDE UCB 200 MG PILLOLI MIKSIJA B’RITA
lacosamide
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, anki jekk għandhom l-istess sinjali ta’
mard bħal tiegħek.
•
Jekk ikollok xi effett sekondarju kellem lit-tabib,jew lill-ispiżjar
jew l-infermier tiegħek. Dan
jinkludi xi effett sekondarju possibbli li m’huwiex elenkat f’dan
il-fuljett. Ara sezzjoni 4.
F’DAN IL-FULJETT:
1.
X’inhu Lacosamide UCB u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tieħu Lacosamide UCB
3.
Kif għandek tieħu Lacosamide UCB
4.
Effetti sekondarji possibli
5.
Kif taħżen Lacosamide UCB
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU LACOSAMIDE UCB U GЋALXIEX JINTUŻA
X’INHU LACOSAMIDE UCB
Lacosamide UCB fih lacosamide. Dan jappartjeni għal grupp ta’
mediċini li jissejħu “mediċini kontra
l-epilessija”. Dawn il-mediċini jintużaw biex jittrattaw
l-epilessija.
•
Int ingħatajt din il-mediċina biex tnaqqas in-numru ta’
aċċessjonijiet li għandek.
GĦALXIEX JINTUŻA LACOSAMIDE UCB
•
Lacosamide UCB jintuża:

waħdu jew flimkien ma’ mediċini oħrajn kontra l-epilessija
fl-adulti, fl-adolexxenti u
fit-tfal minn età ta’ sentejn u aktar biex jittratta ċertu tip
ta’ epilessija kkaratterizzata
bl-okkorrenza ta’ aċċessjonijiet tat-tip feġġa parzjali kemm
b’ġeneralizzazzjoni
sekondarja kif ukoll mingħajr. F’dan it-tip ta’ epilessija,
l-aċċessjonijiet l-ewwel
ikollhom effett fuq naħa waħda biss ta’ mo
                                
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Summary of Product characteristics

                                1
_ _
ANNESS I
SOMMARJU TAL-KARATTERISTIKI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Lacosamide UCB 50 mg pilloli miksijin b’rita
Lacosamide UCB 100 mg pilloli miksijin b’rita
Lacosamide UCB 150 mg pilloli miksijin b’rita
Lacosamide UCB 200 mg pilloli miksijin b’rita
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
_ _
Lacosamide UCB 50 mg pilloli miksijin b’rita
Kull pillola miksija b’rita fiha 50 mg lacosamide.
Lacosamide UCB 100 mg pilloli miksijin b’rita
Kull pillola miksija b’rita fiha 100 mg lacosamide.
Lacosamide UCB 150 mg pilloli miksijin b’rita
Kull pillola miksija b’rita fiha 150 mg lacosamide.
Lacosamide UCB 200 mg pilloli miksijin b’rita
Kull pillola miksija b’rita fiha 200 mg lacosamide.
Għal-lista sħiħa ta’ eċċipjenti, ara s-sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Pillola miksija b’rita.
Lacosamide UCB 50 mg pilloli miksijin b’rita
Pilloli miksijin b’rita ovali, jagħtu fir-roża, b’dimensjonijiet
ta’ madwar 10.4 mm x 4.9 mm, u
mnaqqxin b’‘SP’ fuq naħa waħda u b’‘50’ fuq in-naħa
l-oħra.
Lacosamide UCB 100 mg pilloli miksijin b’rita
Pilloli miksijin b’rita ovali, sofor skuri b’dimensjonijiet ta’
madwar 13.2 mm x 6.1 mm, u mnaqqxin
b’‘SP’ fuq naħa waħda u b’‘100’ fuq in-naħa l-oħra.
Lacosamide UCB 150 mg pilloli miksijin b’rita
Pilloli miksijin b’rita ovali, kulur is-salamun, b’dimensjonijiet
ta’ madwar 15.1 mm x 7.0 mm, u
mnaqqxin b’‘SP’ fuq naħa waħda u b’‘150’ fuq in-naħa
l-oħra.
Lacosamide UCB 200 mg pilloli miksijin b’rita
Pilloli miksijin b’rita ovali, blu, b’dimensjonijiet ta’ madwar
16.6 mm x 7.8 mm, u mnaqqxin b’‘SP’
fuq naħa waħda u b’‘200’ fuq in-naħa l-oħra.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Lacosamide UCB huwa indikat bħala monoterapija fit-trattament ta’
aċċessjonijiet tat-tip ‘partial-
onset’ kemm b’ġeneralizzazzjoni sekondarja kif ukoll mingħajr,
f’adulti, adolexxenti u tfal mill-età ta’
sentejn b’epilessija.
3
Lacosamide UCB
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 25-01-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 25-01-2023
Public Assessment Report Public Assessment Report Bulgarian 25-03-2024
Patient Information leaflet Patient Information leaflet Spanish 25-01-2023
Public Assessment Report Public Assessment Report Spanish 25-03-2024
Patient Information leaflet Patient Information leaflet Czech 25-01-2023
Public Assessment Report Public Assessment Report Czech 25-03-2024
Patient Information leaflet Patient Information leaflet Danish 25-01-2023
Public Assessment Report Public Assessment Report Danish 25-03-2024
Patient Information leaflet Patient Information leaflet German 25-01-2023
Public Assessment Report Public Assessment Report German 25-03-2024
Patient Information leaflet Patient Information leaflet Estonian 25-01-2023
Public Assessment Report Public Assessment Report Estonian 25-03-2024
Patient Information leaflet Patient Information leaflet Greek 25-01-2023
Public Assessment Report Public Assessment Report Greek 25-03-2024
Patient Information leaflet Patient Information leaflet English 25-01-2023
Public Assessment Report Public Assessment Report English 25-03-2024
Patient Information leaflet Patient Information leaflet French 25-01-2023
Public Assessment Report Public Assessment Report French 25-03-2024
Patient Information leaflet Patient Information leaflet Italian 25-01-2023
Public Assessment Report Public Assessment Report Italian 25-03-2024
Patient Information leaflet Patient Information leaflet Latvian 25-01-2023
Public Assessment Report Public Assessment Report Latvian 25-03-2024
Patient Information leaflet Patient Information leaflet Lithuanian 25-01-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 25-01-2023
Public Assessment Report Public Assessment Report Lithuanian 25-03-2024
Patient Information leaflet Patient Information leaflet Hungarian 25-01-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 25-01-2023
Public Assessment Report Public Assessment Report Hungarian 25-03-2024
Patient Information leaflet Patient Information leaflet Dutch 25-01-2023
Public Assessment Report Public Assessment Report Dutch 25-03-2024
Patient Information leaflet Patient Information leaflet Polish 25-01-2023
Public Assessment Report Public Assessment Report Polish 25-03-2024
Patient Information leaflet Patient Information leaflet Portuguese 25-01-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 25-01-2023
Public Assessment Report Public Assessment Report Portuguese 25-03-2024
Patient Information leaflet Patient Information leaflet Romanian 25-01-2023
Public Assessment Report Public Assessment Report Romanian 25-03-2024
Patient Information leaflet Patient Information leaflet Slovak 25-01-2023
Public Assessment Report Public Assessment Report Slovak 25-03-2024
Patient Information leaflet Patient Information leaflet Slovenian 25-01-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 25-01-2023
Public Assessment Report Public Assessment Report Slovenian 25-03-2024
Patient Information leaflet Patient Information leaflet Finnish 25-01-2023
Public Assessment Report Public Assessment Report Finnish 25-03-2024
Patient Information leaflet Patient Information leaflet Swedish 25-01-2023
Public Assessment Report Public Assessment Report Swedish 25-03-2024
Patient Information leaflet Patient Information leaflet Norwegian 25-01-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 25-01-2023
Patient Information leaflet Patient Information leaflet Icelandic 25-01-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 25-01-2023
Patient Information leaflet Patient Information leaflet Croatian 25-01-2023
Public Assessment Report Public Assessment Report Croatian 25-03-2024

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