Briviact (in Italy: Nubriveo)

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

Brivaracetam

Available from:

UCB Pharma SA

ATC code:

N03AX23

INN (International Name):

brivaracetam

Therapeutic group:

Anti-epilettiċi,

Therapeutic area:

Epilessija

Therapeutic indications:

Briviact huwa indikat bħala terapija aġġuntiva fit-trattament ta 'aċċessjonijiet ta' bidu parzjali bi jew mingħajr ġeneralizzazzjoni sekondarja f'pazjenti adulti u adolexxenti minn 16-il sena b'epilessija.

Product summary:

Revision: 22

Authorization status:

Awtorizzat

Authorization date:

2016-01-13

Patient Information leaflet

                                100
B. FULJETT TA’ TAGĦRIF
101
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-PAZJENT
BRIVIACT 10 MG PILLOLI MIKSIJA B’RITA
BRIVIACT 25 MG PILLOLI MIKSIJA B’RITA
BRIVIACT 50 MG PILLOLI MIKSIJA B’RITA
BRIVIACT 75 MG PILLOLI MIKSIJA B’RITA
BRIVIACT 100 MG PILLOLI MIKSIJA B’RITA
Brivaracetam
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 ikollhom l-istess sinjali ta’ mard
bħal tiegħek.
-
Jekk ikollok xi effett sekondarju kellem lit-tabib, jew
lill-ispiżjar. Dan jinkludi xi effett
sekondarju possibbli li mhuwiex elenkat f’dan il-fuljett. Ara
sezzjoni 4.
F’DAN IL-FULJETT:
1.
X’inhu Briviact u għalxiex jintuża
2.
X’għandek tkun taf qabel ma tieħu Briviact
3.
Kif għandek tieħu Briviact
4.
Effetti sekondarji possibbli
5.
Kif taħżen Briviact
6.
Kontenut tal-pakkett u informazzjoni oħra
1.
X’INHU BRIVIACT U GЋALXIEX JINTUŻA
X’INHU BRIVIACT
Briviact fih is-sustanza attiva brivaracetam. Dan jagħmel parti minn
grupp ta’ mediċini li jisimhom
‘mediċini kontra l-epilessija’. Dawn il-mediċini jintużaw
fit-trattament tal-epilessija.
GĦAL XIEX JINTUŻA BRIVIACT
-
Briviact jintuża f’adulti, adoloxxenti u tfal minn età ta’
sentejn ’il fuq.
-
Huwa użat fit-trattament ta’ tip ta’ epilessija
b’aċċessjonijiet parzjali bi jew mingħajr
ġeneralizzazzjoni sekondarja.
-
Aċċessjonijiet parzjali huma aċċessjonijiet li jibdew billi
jaffetwaw naħa waħda biss tal-moħħ.
Dawn jistgħu jinfirxu u jilħqu partijiet akbar fiż-żewġt naħat
tal-moħħ – dan jissejjaħ
‘ġeneralizzazzjoni sekondarja’.
-
Din il-mediċina ġie mogħtija lilek sabiex tnaqqaslek in-numru ta’
aċċessjonijiet li jkollok.
-
Briviact huwa użat flim
                                
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Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Briviact 10 mg pilloli miksija b’rita
Briviact 25 mg pilloli miksija b’rita
Briviact 50 mg pilloli miksija b’rita
Briviact 75 mg pilloli miksija b’rita
Briviact 100 mg pilloli miksija b’rita
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
_ _
Briviact 10 mg pilloli miksija b’rita
Kull pillola miksija b’rita fiha 10 mg brivaracetam.
Briviact 25 mg pilloli miksija b’rita
Kull pillola miksija b’rita fiha 25 mg brivaracetam.
Briviact 50 mg pilloli miksija b’rita
Kull pillola miksija b’rita fiha 50 mg brivaracetam.
Briviact 75 mg pilloli miksija b’rita
Kull pillola miksija b’rita fiha 75 mg brivaracetam.
Briviact 100 mg pilloli miksija b’rita
Kull pillola miksija b’rita fiha 100 mg brivaracetam.
Eċċipjent(i) b’effett magħruf:
Briviact 10 mg pilloli miksija b’rita
Kull pillola miksija b’rita 10 mg fiha 88 mg lactose.
Briviact 25 mg pilloli miksija b’rita
Kull pillola miksija b’rita 25 mg fiha 94 mg lactose.
Briviact 50 mg pilloli miksija b’rita
Kull pillola miksija b’rita 50 mg fiha 189 mg lactose.
Briviact 75 mg pilloli miksija b’rita
Kull pillola miksija b’rita 75 mg fiha 283 mg lactose.
Briviact 100 mg pilloli miksija b’rita
Kull pillola miksija b’rita 100 mg fiha 377 mg lactose.
Għal-lista kompluta ta’ eċċipjenti, ara sezzjoni 6.1.
3
3.
GĦAMLA FARMAĊEWTIKA
Pillola miksija b’rita (pillola)
Briviact 10 mg pilloli miksija b’rita
Pilloli miksija b’rita bajda għal abjad imdennes, tondi, ta’
dijametru ta’ 6.5 mm u mnaqqxa b’‘u10’
fuq naħa waħda.
Briviact 25 mg pilloli miksija b’rita
Pilloli miksija b’rita griża, ovali, b’dimensjonijiet ta’ 8.9 x
5.0 mm u mnaqqxa b’‘u25’ fuq naħa
waħda.
Briviact 50 mg pilloli miksija b’rita
Pilloli miksija b’rita safra, ovali, b’dimensjonijiet ta’ 11.7
mm x 6.6 mm u mnaqqxa b’‘u50’ fuq naħa
waħda.
Briviact 75 mg pilloli miksija b’rita
Pilloli miksija b’rita vjola, ovali, b’dimensjonijiet ta’ 1
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 10-01-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 10-01-2024
Public Assessment Report Public Assessment Report Bulgarian 17-03-2022
Patient Information leaflet Patient Information leaflet Spanish 10-01-2024
Public Assessment Report Public Assessment Report Spanish 17-03-2022
Patient Information leaflet Patient Information leaflet Czech 10-01-2024
Public Assessment Report Public Assessment Report Czech 17-03-2022
Patient Information leaflet Patient Information leaflet Danish 10-01-2024
Public Assessment Report Public Assessment Report Danish 17-03-2022
Patient Information leaflet Patient Information leaflet German 10-01-2024
Public Assessment Report Public Assessment Report German 17-03-2022
Patient Information leaflet Patient Information leaflet Estonian 10-01-2024
Public Assessment Report Public Assessment Report Estonian 17-03-2022
Patient Information leaflet Patient Information leaflet Greek 10-01-2024
Public Assessment Report Public Assessment Report Greek 17-03-2022
Patient Information leaflet Patient Information leaflet English 10-01-2024
Public Assessment Report Public Assessment Report English 17-03-2022
Patient Information leaflet Patient Information leaflet French 10-01-2024
Public Assessment Report Public Assessment Report French 17-03-2022
Patient Information leaflet Patient Information leaflet Italian 10-01-2024
Public Assessment Report Public Assessment Report Italian 17-03-2022
Patient Information leaflet Patient Information leaflet Latvian 10-01-2024
Public Assessment Report Public Assessment Report Latvian 17-03-2022
Patient Information leaflet Patient Information leaflet Lithuanian 10-01-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 10-01-2024
Public Assessment Report Public Assessment Report Lithuanian 17-03-2022
Patient Information leaflet Patient Information leaflet Hungarian 10-01-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 10-01-2024
Public Assessment Report Public Assessment Report Hungarian 17-03-2022
Patient Information leaflet Patient Information leaflet Dutch 10-01-2024
Public Assessment Report Public Assessment Report Dutch 17-03-2022
Patient Information leaflet Patient Information leaflet Polish 10-01-2024
Public Assessment Report Public Assessment Report Polish 17-03-2022
Patient Information leaflet Patient Information leaflet Portuguese 10-01-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 10-01-2024
Public Assessment Report Public Assessment Report Portuguese 17-03-2022
Patient Information leaflet Patient Information leaflet Romanian 10-01-2024
Public Assessment Report Public Assessment Report Romanian 17-03-2022
Patient Information leaflet Patient Information leaflet Slovak 10-01-2024
Public Assessment Report Public Assessment Report Slovak 17-03-2022
Patient Information leaflet Patient Information leaflet Slovenian 10-01-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 10-01-2024
Public Assessment Report Public Assessment Report Slovenian 17-03-2022
Patient Information leaflet Patient Information leaflet Finnish 10-01-2024
Public Assessment Report Public Assessment Report Finnish 17-03-2022
Patient Information leaflet Patient Information leaflet Swedish 10-01-2024
Public Assessment Report Public Assessment Report Swedish 17-03-2022
Patient Information leaflet Patient Information leaflet Norwegian 10-01-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 10-01-2024
Patient Information leaflet Patient Information leaflet Icelandic 10-01-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 10-01-2024
Patient Information leaflet Patient Information leaflet Croatian 10-01-2024
Public Assessment Report Public Assessment Report Croatian 17-03-2022

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