Vimpat

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

lakosamid

Available from:

UCB Pharma SA

ATC code:

N03AX18

INN (International Name):

lacosamide

Therapeutic group:

Antiepileptics,

Therapeutic area:

Epilepsija

Therapeutic indications:

Zdravilo Vimpat je indicirano kot monoterapija in dodatno zdravljenje pri zdravljenju epileptičnih napadov s sekundarno generalizacijo ali brez nje pri odraslih, mladostnikih in otrocih od 4. leta starosti z epilepsijo.

Product summary:

Revision: 46

Authorization status:

Pooblaščeni

Authorization date:

2008-08-29

Patient Information leaflet

                                84
10.
POSEBNI VARNOSTNI UKREPI ZA ODSTRANJEVANJE NEUPORABLJENIH
ZDRAVIL ALI IZ NJIH NASTALIH ODPADNIH SNOVI, KADAR SO POTREBNI
11.
IME IN NASLOV IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
UCB Pharma S.A.
Allée de la Recherche 60
B-1070 Bruxelles
Belgija
12.
ŠTEVILKA(E) DOVOLJENJA (DOVOLJENJ) ZA PROMET
EU/1/08/470/001 14 filmsko obloženih tablet
EU/1/08/470/002 56 filmsko obloženih tablet
EU/1/08/470/003 168 filmsko obloženih tablet
EU/1/08/470/020 56 x 1 filmsko obložena tableta
EU/1/08/470/024 14 x 1 filmsko obložena tableta
EU/1/08/470/025 28 filmsko obloženih tablet
EU/1/08/470/032 60 filmsko obloženih tablet
13.
ŠTEVILKA SERIJE
Lot
14.
NAČIN IZDAJANJA ZDRAVILA
15.
NAVODILA ZA UPORABO
16.
PODATKI V BRAILLOVI PISAVI
Vimpat 50 mg
 56 x 1 in 14 x 1
filmsko obložena tableta
17.
EDINSTVENA OZNAKA – DVODIMENZIONALNA ČRTNA KODA
_ _
Vsebuje dvodimenzionalno črtno kodo z edinstveno oznako.
18.
EDINSTVENA OZNAKA – V BERLJIVI OBLIKI
_ _
PC
SN
NN
85
PODATKI, KI MORAJO BITI NAJMANJ NAVEDENI NA PRETISNEM OMOTU ALI
DVOJNEM TRAKU
PRETISNI OMOT
1.
IME ZDRAVILA
Vimpat 50 mg filmsko obložene tablete
 Vimpat 50 mg tablete
lakozamid
2.
IME IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
UCB Pharma S.A.
3.
DATUM IZTEKA ROKA UPORABNOSTI ZDRAVILA
EXP
4.
ŠTEVILKA SERIJE
Lot
5.
DRUGI PODATKI
86
PODATKI NA PRIMARNI OVOJNINI
PLASTENKA
1.
IME ZDRAVILA
Vimpat 50 mg filmsko obložene tablete
lakozamid
2.
NAVEDBA ENE ALI VEČ UČINKOVIN
Ena filmsko obložena tableta vsebuje 50 mg lakozamida.
3.
SEZNAM POMOŽNIH SNOVI
4.
FARMACEVTSKA OBLIKA IN VSEBINA
60 filmsko obloženih tablet
5.
POSTOPEK IN POT(I) UPORABE ZDRAVILA
Pred uporabo preberite priloženo navodilo!
za peroralno uporabo
6.
POSEBNO OPOZORILO O SHRANJEVANJU ZDRAVILA ZUNAJ DOSEGA IN
POGLEDA OTROK
Zdravilo shranjujte nedosegljivo otrokom!
7.
DRUGA POSEBNA OPOZORILA, ČE SO POTREBNA
8.
DATUM IZTEKA ROKA UPORABNOSTI ZDRAVILA
EXP
9.
POSEBNA NAVODILA ZA SHRANJEVANJE
10.
POSEBNI 
                                
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Summary of Product characteristics

                                1
PRILOGA I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
2
1. IME ZDRAVILA
Vimpat 50 mg filmsko obložene tablete
Vimpat 100 mg filmsko obložene tablete
Vimpat 150 mg filmsko obložene tablete
Vimpat 200 mg filmsko obložene tablete
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Vimpat 50 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 50 mg lakozamida.
Vimpat 100 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 100 mg lakozamida.
Vimpat 150 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 150 mg lakozamida.
Vimpat 200 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 200 mg lakozamida.
Za celoten seznam pomožnih snovi glejte poglavje 6.1.
3.
FARMACEVTSKA OBLIKA
filmsko obložena tableta
Vimpat 50 mg filmsko obložene tablete
Rožnate, ovalne filmsko obložene tablete z merami približno 10,4 mm
x 4,9 mm, z vtisnjeno oznako
‘SP’ na eni strani in oznako ‘50’ na drugi strani.
Vimpat 100 mg filmsko obložene tablete
Temno rumene, ovalne filmsko obložene tablete z merami približno
13,2 mm x 6,1 mm, z vtisnjeno
oznako ‘SP’ na eni strani in oznako ‘100’ na drugi strani.
Vimpat 150 mg filmsko obložene tablete
Lososovo rožnate, ovalne filmsko obložene tablete z merami
približno 15,1 mm x 7,0 mm, z vtisnjeno
oznako ‘SP’ na eni strani in oznako ‘150’ na drugi strani.
Vimpat 200 mg filmsko obložene tablete
Modre, ovalne filmsko obložene tablete z merami približno 16,6 mm x
7,8 mm, z vtisnjeno oznako
‘SP’ na eni strani in oznako ‘200’ na drugi strani.
4.
KLINIČNI PODATKI
4.1
TERAPEVTSKE INDIKACIJE
Zdravilo Vimpat je indicirano za samostojno zdravljenje parcialnih
napadov s sekundarno
generalizacijo ali brez nje pri odraslih, mladostnikih in otrocih od
2. leta starosti z epilepsijo.
3
Zdravilo Vimpat je indicirano za dopolnilno zdravljenje
•
parcialnih napadov s sekundarno generalizacijo ali brez nje pri
odraslih, mladostnikih in
otrocih od 2. leta starosti z epilepsijo,
•
primarno generaliziranih tonično-kloničnih napado
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 08-01-2024
Public Assessment Report Public Assessment Report Bulgarian 25-03-2024
Patient Information leaflet Patient Information leaflet Spanish 08-01-2024
Public Assessment Report Public Assessment Report Spanish 25-03-2024
Patient Information leaflet Patient Information leaflet Czech 08-01-2024
Public Assessment Report Public Assessment Report Czech 25-03-2024
Patient Information leaflet Patient Information leaflet Danish 08-01-2024
Public Assessment Report Public Assessment Report Danish 25-03-2024
Patient Information leaflet Patient Information leaflet German 08-01-2024
Public Assessment Report Public Assessment Report German 25-03-2024
Patient Information leaflet Patient Information leaflet Estonian 08-01-2024
Public Assessment Report Public Assessment Report Estonian 25-03-2024
Patient Information leaflet Patient Information leaflet Greek 08-01-2024
Public Assessment Report Public Assessment Report Greek 25-03-2024
Patient Information leaflet Patient Information leaflet English 08-01-2024
Public Assessment Report Public Assessment Report English 25-03-2024
Patient Information leaflet Patient Information leaflet French 08-01-2024
Public Assessment Report Public Assessment Report French 25-03-2024
Patient Information leaflet Patient Information leaflet Italian 08-01-2024
Public Assessment Report Public Assessment Report Italian 25-03-2024
Patient Information leaflet Patient Information leaflet Latvian 08-01-2024
Public Assessment Report Public Assessment Report Latvian 25-03-2024
Patient Information leaflet Patient Information leaflet Lithuanian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 08-01-2024
Public Assessment Report Public Assessment Report Lithuanian 25-03-2024
Patient Information leaflet Patient Information leaflet Hungarian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 08-01-2024
Public Assessment Report Public Assessment Report Hungarian 25-03-2024
Patient Information leaflet Patient Information leaflet Maltese 08-01-2024
Public Assessment Report Public Assessment Report Maltese 25-03-2024
Patient Information leaflet Patient Information leaflet Dutch 08-01-2024
Public Assessment Report Public Assessment Report Dutch 25-03-2024
Patient Information leaflet Patient Information leaflet Polish 08-01-2024
Public Assessment Report Public Assessment Report Polish 25-03-2024
Patient Information leaflet Patient Information leaflet Portuguese 08-01-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 08-01-2024
Public Assessment Report Public Assessment Report Portuguese 25-03-2024
Patient Information leaflet Patient Information leaflet Romanian 08-01-2024
Public Assessment Report Public Assessment Report Romanian 25-03-2024
Patient Information leaflet Patient Information leaflet Slovak 08-01-2024
Public Assessment Report Public Assessment Report Slovak 25-03-2024
Patient Information leaflet Patient Information leaflet Finnish 08-01-2024
Public Assessment Report Public Assessment Report Finnish 25-03-2024
Patient Information leaflet Patient Information leaflet Swedish 08-01-2024
Public Assessment Report Public Assessment Report Swedish 25-03-2024
Patient Information leaflet Patient Information leaflet Norwegian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 08-01-2024
Patient Information leaflet Patient Information leaflet Icelandic 08-01-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 08-01-2024
Patient Information leaflet Patient Information leaflet Croatian 08-01-2024
Public Assessment Report Public Assessment Report Croatian 25-03-2024

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