Entacapone Teva

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

tableta

Available from:

Teva Pharma B.V.

ATC code:

N04BX02

INN (International Name):

entacapone

Therapeutic group:

Antiparkinsonski lijekovi

Therapeutic area:

Parkinsonova bolest

Therapeutic indications:

Entacapone je indiciran kao dodatak standardnim pripremama levodope / benserazide ili levodope / carbidopa u odraslih bolesnika s Parkinsonovom bolesti i kraju doze motoričke fluktuacije, koji mogu biti stabilizirani te kombinacije.

Product summary:

Revision: 10

Authorization status:

odobren

Authorization date:

2011-02-18

Patient Information leaflet

                                20
B. UPUTA O LIJEKU
21
UPUTA O LIJEKU: INFORMACIJA ZA KORISNIKA
ENTAKAPON TEVA 200 MG FILMOM OBLOŽENE TABLETE
entakapon
PAŽLJIVO PROČITAJTE CIJELU UPUTU PRIJE NEGO POČNETE UZIMATI OVAJ
LIJEK JER SADRŽI VAMA VAŽNE
PODATKE.
-
Sačuvajte ovu uputu. Možda ćete je trebati ponovno pročitati.
-
Ako imate dodatnih pitanja, obratite se svom liječniku ili
ljekarniku.
-
Ovaj je lijek propisan samo Vama. Nemojte ga davati drugima. Može im
naškoditi, čak i ako su
njihovi znakovi bolesti jednaki Vašima.
-
Ako primijetite bilo koju nuspojavu, potrebno je obavijestiti
liječnika ili ljekarnika. To uključuje
i svaku moguću nuspojavu koja nije navedena u ovoj uputi. Pogledajte
dio 4.
ŠTO SE NALAZI U OVOJ UPUTI:
1.
Što je Entakapon Teva i za što se koristi
2.
Što morate znati prije nego počnete uzimati Entakapon Teva
3.
Kako uzimati Entakapon Teva
4.
Moguće nuspojave
5.
Kako čuvati Entakapon Teva
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE ENTAKAPON TEVA I ZA ŠTO SE KORISTI
Entakapon Teva tablete sadrže entakapon i primjenjuju se zajedno s
levodopom za liječenje
Parkinsonove bolesti. Entakapon Teva pomaže levodopi u ublažavanju
simptoma Parkinsonove
bolesti. Entakapon Teva nema učinak na ublažavanje simptoma
Parkinsonove bolesti ako nije uzet s
levodopom.
2.
ŠTO MORATE ZNATI PRIJE NEGO POČNETE UZIMATI ENTAKAPON TEVA
NEMOJTE UZIMATI ENTAKAPON TEVA
•
ako ste alergični na entakapon ili neki drugi sastojak ovog lijeka
(naveden u dijelu 6);
•
ako imate tumor nadbubrežne žlijezde (poznat pod nazivom
feokromocitom; jer to može
povećati rizik od izrazitog povišenja krvnog tlaka);
•
ako uzimate određene lijekove protiv depresije (upitajte svog
liječnika ili ljekarnika može li se
Vaš lijek protiv depresije uzimati zajedno s Entakaponom Teva);
•
ako imate bolest jetre;
•
ako ste ikad imali rijetku reakciju na antipsihotike zvanu
neuroleptički maligni sindrom
(NMS). Pogledajte dio 4. Moguće nuspojave za karakteristike NMS-a;
•
ako ste ikad patili od rijetkog mišićnog poremeća
                                
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Summary of Product characteristics

                                1
DODATAK I
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Entakapon Teva 200 mg filmom obložene tablete
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Jedna filmom obložena tableta sadrži 200 mg entakapona.
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Filmom obložena tableta.
Svijetlosmeđe, bikonveksne, filmom obložene tablete eliptičnog
oblika, duljine oko 18 mm i širine 10
mm, s otisnutom oznakom "E200" na jednoj strani te bez oznake na
drugoj strani.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Entakapon je indiciran kao dodatak standardnim preparatima
levodope/benzerazida ili
levodope/karbidope, za primjenu u odraslih bolesnika s Parkinsonovom
bolešću i motoričkim
fluktuacijama pri kraju doze koji se ne mogu stabilizirati tim
kombinacijama.
_ _
4.2
DOZIRANJE I NAČIN PRIMJENE
Entakapon treba primjenjivati samo u kombinaciji s
levodopom/benzerazidom ili
levodopom/karbidopom. Uputa za propisivanje tih preparata levodope
primjenjiva je i za njihovu
istovremenu primjenu s entakaponom.
Doziranje
Jedna tableta od 200 mg uzima se sa svakom dozom levodope/inhibitora
dopa dekarboksilaze.
Maksimalna preporučena doza je 200 mg deset puta dnevno, odnosno 2000
mg entakapona.
Entakapon pojačava učinke levodope. Zato je tijekom prvih dana ili
prvih tjedana od početka
liječenja entakaponom često potrebno prilagoditi doziranje levodope
kako bi se smanjile
dopaminergičke nuspojave povezane s levodopom, npr. diskinezije,
mučnina, povraćanje i
halucinacije. Dnevnu dozu levodope treba smanjiti za oko 10-30%, što
se postiže produljenjem
intervala doziranja i/ili smanjenjem količine levodope po dozi, u
skladu s kliničkim stanjem
bolesnika.
Ako se liječenje entakaponom prekine, nužno je prilagoditi doziranje
ostalih lijekova za
Parkinsonovu bolest, posebno levodope, kako bi se postigao
zadovoljavajući nadzor nad simptomima
Parkinsonove bolesti.
Entakapon povećava bioraspoloživost levodope iz standardnih
preparata levodope/benzerazida nešto
više (5-10%) nego iz standardnih prep
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 28-09-2021
Summary of Product characteristics Summary of Product characteristics Bulgarian 28-09-2021
Public Assessment Report Public Assessment Report Bulgarian 28-01-2016
Patient Information leaflet Patient Information leaflet Spanish 28-09-2021
Public Assessment Report Public Assessment Report Spanish 28-01-2016
Patient Information leaflet Patient Information leaflet Czech 28-09-2021
Public Assessment Report Public Assessment Report Czech 28-01-2016
Patient Information leaflet Patient Information leaflet Danish 28-09-2021
Public Assessment Report Public Assessment Report Danish 28-01-2016
Patient Information leaflet Patient Information leaflet German 28-09-2021
Public Assessment Report Public Assessment Report German 28-01-2016
Patient Information leaflet Patient Information leaflet Estonian 28-09-2021
Public Assessment Report Public Assessment Report Estonian 28-01-2016
Patient Information leaflet Patient Information leaflet Greek 28-09-2021
Public Assessment Report Public Assessment Report Greek 28-01-2016
Patient Information leaflet Patient Information leaflet English 28-09-2021
Public Assessment Report Public Assessment Report English 28-01-2016
Patient Information leaflet Patient Information leaflet French 28-09-2021
Public Assessment Report Public Assessment Report French 28-01-2016
Patient Information leaflet Patient Information leaflet Italian 28-09-2021
Public Assessment Report Public Assessment Report Italian 28-01-2016
Patient Information leaflet Patient Information leaflet Latvian 28-09-2021
Public Assessment Report Public Assessment Report Latvian 28-01-2016
Patient Information leaflet Patient Information leaflet Lithuanian 28-09-2021
Summary of Product characteristics Summary of Product characteristics Lithuanian 28-09-2021
Public Assessment Report Public Assessment Report Lithuanian 28-01-2016
Patient Information leaflet Patient Information leaflet Hungarian 28-09-2021
Summary of Product characteristics Summary of Product characteristics Hungarian 28-09-2021
Public Assessment Report Public Assessment Report Hungarian 28-01-2016
Patient Information leaflet Patient Information leaflet Maltese 28-09-2021
Public Assessment Report Public Assessment Report Maltese 28-01-2016
Patient Information leaflet Patient Information leaflet Dutch 28-09-2021
Public Assessment Report Public Assessment Report Dutch 28-01-2016
Patient Information leaflet Patient Information leaflet Polish 28-09-2021
Public Assessment Report Public Assessment Report Polish 28-01-2016
Patient Information leaflet Patient Information leaflet Portuguese 28-09-2021
Summary of Product characteristics Summary of Product characteristics Portuguese 28-09-2021
Public Assessment Report Public Assessment Report Portuguese 28-01-2016
Patient Information leaflet Patient Information leaflet Romanian 28-09-2021
Public Assessment Report Public Assessment Report Romanian 28-01-2016
Patient Information leaflet Patient Information leaflet Slovak 28-09-2021
Public Assessment Report Public Assessment Report Slovak 28-01-2016
Patient Information leaflet Patient Information leaflet Slovenian 28-09-2021
Summary of Product characteristics Summary of Product characteristics Slovenian 28-09-2021
Public Assessment Report Public Assessment Report Slovenian 28-01-2016
Patient Information leaflet Patient Information leaflet Finnish 28-09-2021
Public Assessment Report Public Assessment Report Finnish 28-01-2016
Patient Information leaflet Patient Information leaflet Swedish 28-09-2021
Public Assessment Report Public Assessment Report Swedish 28-01-2016
Patient Information leaflet Patient Information leaflet Norwegian 28-09-2021
Summary of Product characteristics Summary of Product characteristics Norwegian 28-09-2021
Patient Information leaflet Patient Information leaflet Icelandic 28-09-2021
Summary of Product characteristics Summary of Product characteristics Icelandic 28-09-2021

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