Zeposia

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

ozanimod hidroklorid

Available from:

Bristol-Myers Squibb Pharma EEIG

ATC code:

L04AA38

INN (International Name):

ozanimod

Therapeutic group:

imunosupresivi

Therapeutic area:

Multiple Sclerosis, Relapsing-Remitting; Colitis, Ulcerative

Therapeutic indications:

Multiple sclerosisZeposia is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (RRMS) with active disease as defined by clinical or imaging features. Ulcerative colitisZeposia is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (UC) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent.

Product summary:

Revision: 5

Authorization status:

odobren

Authorization date:

2020-05-20

Patient Information leaflet

                                41
B. UPUTA O LIJEKU
42
UPUTA O LIJEKU: INFORMACIJE ZA BOLESNIKA
ZEPOSIA 0,23 MG TVRDE KAPSULE
ZEPOSIA 0,46 MG TVRDE KAPSULE
ZEPOSIA 0,92 MG TVRDE KAPSULE
ozanimod
Ovaj je lijek pod dodatnim praćenjem. Time se omogućuje brzo
otkrivanje novih sigurnosnih informacija.
Prijavom svih sumnji na nuspojavu i Vi možete pomoći. Za postupak
prijavljivanja nuspojava, pogledajte
dio 4.
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 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 Zeposia i za što se koristi
2.
Što morate znati prije nego počnete uzimati lijek Zeposia
3.
Kako uzimati lijek Zeposia
4.
Moguće nuspojave
5.
Kako čuvati lijek Zeposia
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE ZEPOSIA I ZA ŠTO SE KORISTI
Zeposia sadrži djelatnu tvar ozanimod koja pripada skupini lijekova
koji mogu smanjiti broj bijelih krvnih
stanica (limfocita) koje slobodno cirkuliraju u tijelu.
Lijek Zeposia namijenjen je za liječenje sljedećih bolesti:
-
multipla skleroza
-
ulcerozni kolitis.
Multipla skleroza
Lijek Zeposia namijenjen je za liječenje odraslih bolesnika s
relapsno-remitirajućom multiplom sklerozom
(RRMS) u kojih je bolest aktivna.
•
Multipla skleroza je bolest kod koje imunosni sustav (obrambeni sustav
tijela koji uključuje i bijele
krvne stanice) pogrešno napada zaštitnu ovojnicu živčanih vlakana
u mozgu i leđnoj moždini. To
zaustavlja ispravan rad živaca i može rezultirati simptomima kao
što su: utrnulost, teškoće pri hodu,
problemi s vidom i ravnotežom.
•
Kod relapsno-remitirajuće mult
                                
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Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
Ovaj je lijek pod dodatnim praćenjem. Time se omogućuje brzo
otkrivanje novih sigurnosnih
informacija. Od zdravstvenih radnika se traži da prijave svaku sumnju
na nuspojavu za ovaj lijek. Za
postupak prijavljivanja nuspojava vidjeti dio 4.8.
1.
NAZIV LIJEKA
Zeposia 0,23 mg tvrde kapsule
Zeposia 0,46 mg tvrde kapsule
Zeposia 0,92 mg tvrde kapsule
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Zeposia 0,23 mg tvrde kapsule
Jedna tvrda kapsula sadrži 0,23 mg ozanimoda u obliku
ozanimodklorida.
Zeposia 0,46 mg tvrde kapsule
Jedna tvrda kapsula sadrži 0,46 mg ozanimoda u obliku
ozanimodklorida.
Zeposia 0,92 mg tvrde kapsule
Jedna tvrda kapsula sadrži 0,92 mg ozanimoda u obliku
ozanimodklorida.
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Tvrda kapsula
Zeposia 0,23 mg tvrde kapsule
Svijetlo siva neprozirna tvrda kapsula, 14,3 mm, s otisnutom crnom
oznakom „OZA“ na kapici i „0.23 mg“
na tijelu.
Zeposia 0,46 mg tvrde kapsule
Tvrda kapsula svijetlo sivog neprozirnog tijela i narančaste
neprozirne kapice, 14,3 mm, s otisnutom crnom
oznakom „OZA“ na kapici i „0.46 mg“ na tijelu.
Zeposia 0,92 mg tvrde kapsule
Narančasta neprozirna tvrda kapsula, 14,3 mm, s otisnutom crnom
oznakom „OZA“ na kapici i „0.92 mg“ na
tijelu.
3
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Multipla skleroza
Lijek Zeposia indiciran je za liječenje odraslih bolesnika s
relapsno-remitirajućom multiplom sklerozom
(RRMS) u kojih je bolest definirana kao aktivna na temelju kliničkih
ili slikovnih pretraga.
Ulcerozni kolitis
Lijek Zeposia indiciran je za liječenje umjerenog do teškog oblika
aktivnog ulceroznog kolitisa u odraslih
bolesnika koji su na liječenje konvencionalnom terapijom ili
biološkim lijekom imali neadekvatan odgovor,
izgubili odgovor ili to liječenje nisu podnosili.
4.2
DOZIRANJE I NAČIN PRIMJENE
Liječenje se mora započeti pod nadzorom liječnika s iskustvom u
liječenju multiple skleroze (MS) ili
ulceroznog kolitisa (UK).
Doziranj
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 03-04-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 03-04-2023
Public Assessment Report Public Assessment Report Bulgarian 21-12-2021
Patient Information leaflet Patient Information leaflet Spanish 03-04-2023
Public Assessment Report Public Assessment Report Spanish 21-12-2021
Patient Information leaflet Patient Information leaflet Czech 03-04-2023
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Public Assessment Report Public Assessment Report Danish 21-12-2021
Patient Information leaflet Patient Information leaflet German 03-04-2023
Public Assessment Report Public Assessment Report German 21-12-2021
Patient Information leaflet Patient Information leaflet Estonian 03-04-2023
Public Assessment Report Public Assessment Report Estonian 21-12-2021
Patient Information leaflet Patient Information leaflet Greek 03-04-2023
Public Assessment Report Public Assessment Report Greek 21-12-2021
Patient Information leaflet Patient Information leaflet English 03-04-2023
Public Assessment Report Public Assessment Report English 21-12-2021
Patient Information leaflet Patient Information leaflet French 03-04-2023
Public Assessment Report Public Assessment Report French 21-12-2021
Patient Information leaflet Patient Information leaflet Italian 03-04-2023
Public Assessment Report Public Assessment Report Italian 21-12-2021
Patient Information leaflet Patient Information leaflet Latvian 03-04-2023
Public Assessment Report Public Assessment Report Latvian 21-12-2021
Patient Information leaflet Patient Information leaflet Lithuanian 03-04-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 03-04-2023
Public Assessment Report Public Assessment Report Lithuanian 21-12-2021
Patient Information leaflet Patient Information leaflet Hungarian 03-04-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 03-04-2023
Public Assessment Report Public Assessment Report Hungarian 21-12-2021
Patient Information leaflet Patient Information leaflet Maltese 03-04-2023
Public Assessment Report Public Assessment Report Maltese 21-12-2021
Patient Information leaflet Patient Information leaflet Dutch 03-04-2023
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Patient Information leaflet Patient Information leaflet Polish 03-04-2023
Public Assessment Report Public Assessment Report Polish 21-12-2021
Patient Information leaflet Patient Information leaflet Portuguese 03-04-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 03-04-2023
Public Assessment Report Public Assessment Report Portuguese 21-12-2021
Patient Information leaflet Patient Information leaflet Romanian 03-04-2023
Public Assessment Report Public Assessment Report Romanian 21-12-2021
Patient Information leaflet Patient Information leaflet Slovak 03-04-2023
Public Assessment Report Public Assessment Report Slovak 21-12-2021
Patient Information leaflet Patient Information leaflet Slovenian 03-04-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 03-04-2023
Public Assessment Report Public Assessment Report Slovenian 21-12-2021
Patient Information leaflet Patient Information leaflet Finnish 03-04-2023
Public Assessment Report Public Assessment Report Finnish 21-12-2021
Patient Information leaflet Patient Information leaflet Swedish 03-04-2023
Public Assessment Report Public Assessment Report Swedish 21-12-2021
Patient Information leaflet Patient Information leaflet Norwegian 03-04-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 03-04-2023
Patient Information leaflet Patient Information leaflet Icelandic 03-04-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 03-04-2023

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