Kisplyx

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

lenvatinib mesilat

Available from:

Eisai GmbH

ATC code:

L01XE29

INN (International Name):

lenvatinib

Therapeutic group:

Antineoplastična sredstva

Therapeutic area:

Karcinom, stanice bubrega

Therapeutic indications:

Kisplyx is indicated for the treatment of adults with advanced renal cell carcinoma (RCC):in combination with pembrolizumab, as first-line treatment (see section 5. in combination with everolimus, following one prior vascular endothelial growth factor (VEGF)-targeted therapy.

Product summary:

Revision: 20

Authorization status:

odobren

Authorization date:

2016-08-25

Patient Information leaflet

                                46
B. UPUTA O LIJEKU
47
UPUTA O LIJEKU: INFORMACIJE ZA KORISNIKA
KISPLYX 4 MG TVRDE KAPSULE
KISPLYX 10 MG TVRDE KAPSULE
lenvatinib
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, ljekarnika ili medicinsku
sestru. To uključuje i svaku moguću nuspojavu koja nije navedena u
ovoj uputi. Pogledajte
dio 4.
ŠTO SE NALAZI U OVOJ UPUTI:
1.
Što je Kisplyx i za što se koristi
2.
Što morate znati prije nego počnete uzimati Kisplyx
3.
Kako uzimati Kisplyx
4.
Moguće nuspojave
5.
Kako čuvati Kisplyx
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE KISPLYX I ZA ŠTO SE KORISTI
ŠTO JE KISPLYX
Kisplyx je lijek koji sadrži djelatnu tvar lenvatinib. Primjenjuje se
u kombinaciji s pembrolizumabom
kao prva linija liječenja za odrasle s uznapredovalim rakom bubrega
(uznapredovali karcinom
bubrežnih stanica). Primjenjuje se i u kombinaciji s everolimusom za
liječenje odraslih bolesnika s
uznapredovalim rakom bubrega kad drugi načini liječenja (tzv.
VEGF-ciljana terapija) nisu pomogli u
zaustavljanju bolesti.
KAKO KISPLYX DJELUJE
Kisplyx blokira djelovanje proteina koji se zovu receptori tirozin
kinaze i uključeni su u razvoj novih
krvnih žila koje stanice opskrbljuju kisikom i hranjivim tvarima i
pomažu njihov rast. Ti proteini
mogu biti prisutni u velikim količinama u stanicama raka, pa
blokiranjem njihovog rada Kisplyx može
usporiti brzinu umnažanja stanica raka i brzinu rasta tumora te
pomoći da se prekine opskrba krvlju
koja je raku potrebna.
2.
ŠTO MORATE ZNATI PRIJE NEGO POČNETE UZIMATI KISPLYX
NEMOJTE UZIMATI KISPLYX:
•
ako ste alergični na lenvatinib ili neki drugi sastojak ovog lijeka

                                
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Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Kisplyx 4 mg tvrde kapsule
Kisplyx 10 mg tvrde kapsule
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Kisplyx 4 mg tvrde kapsule
Jedna tvrda kapsula sadrži 4 mg lenvatiniba (u obliku
lenvatinibmesilata).
Kisplyx 10 mg tvrde kapsule
Jedna tvrda kapsula sadrži 10 mg lenvatiniba (u obliku
lenvatinibmesilata).
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Tvrda kapsula.
Kisplyx 4 mg tvrde kapsule
Žućkasto-crveno tijelo i žućkasto-crvena kapica, približne
duljine 14,3 mm, s oznakom “Є” otisnutom
crnom tintom na kapici i “LENV 4 mg” na tijelu.
Kisplyx 10 mg tvrde kapsule
Žuto tijelo i žućkasto-crvena kapica, približne duljine 14,3 mm, s
oznakom “Є” otisnutom crnom
tintom na kapici i “LENV 10 mg” na tijelu.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Kisplyx je indiciran za liječenje odraslih bolesnika s uznapredovalim
karcinomom bubrežnih stanica
(engl.
_Renal Cell Carcinoma_
, RCC):
•
u kombinaciji s pembrolizumabom kao prva linija liječenja (vidjeti
dio 5.1)
•
u kombinaciji s everolimusom nakon jedne prethodne terapije usmjerene
na vaskularni
endotelni čimbenik rasta (engl.
_Vascular Endothelial Growth Factor_
, VEGF) (vidjeti dio 5.1).
4.2
DOZIRANJE I NAČIN PRIMJENE
Liječenje treba započeti i nadzirati zdravstveni radnik s iskustvom
u primjeni terapija protiv raka.
Doziranje
_Kisplyx u kombinaciji s pembrolizumabom kao prva linija liječenja_
Preporučena doza lenvatiniba iznosi 20 mg (dvije kapsule od 10 mg)
peroralno jedanput na dan u
kombinaciji s pembrolizumabom 200 mg svaka 3 tjedna ili 400 mg svakih
6 tjedana primijenjeno kao
intravenska infuzija u trajanju od 30 minuta. Dnevnu dozu treba
prilagoditi po potrebi u skladu s
planom određivanja doze s obzirom na toksičnost. Liječenje
lenvatinibom treba nastaviti do progresije
3
bolesti ili pojave neprihvatljive toksičnosti. Liječenje
pembrolizumabom treba nastaviti do progresije
bolesti, pojave neprihvatljive toksičnosti ili do kraja li
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 04-01-2024
Public Assessment Report Public Assessment Report Bulgarian 30-11-2021
Patient Information leaflet Patient Information leaflet Spanish 04-01-2024
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Patient Information leaflet Patient Information leaflet Danish 04-01-2024
Public Assessment Report Public Assessment Report Danish 30-11-2021
Patient Information leaflet Patient Information leaflet German 04-01-2024
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Patient Information leaflet Patient Information leaflet Estonian 04-01-2024
Public Assessment Report Public Assessment Report Estonian 30-11-2021
Patient Information leaflet Patient Information leaflet Greek 04-01-2024
Public Assessment Report Public Assessment Report Greek 30-11-2021
Patient Information leaflet Patient Information leaflet English 04-01-2024
Public Assessment Report Public Assessment Report English 30-11-2021
Patient Information leaflet Patient Information leaflet French 04-01-2024
Public Assessment Report Public Assessment Report French 30-11-2021
Patient Information leaflet Patient Information leaflet Italian 04-01-2024
Public Assessment Report Public Assessment Report Italian 30-11-2021
Patient Information leaflet Patient Information leaflet Latvian 04-01-2024
Public Assessment Report Public Assessment Report Latvian 30-11-2021
Patient Information leaflet Patient Information leaflet Lithuanian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 04-01-2024
Public Assessment Report Public Assessment Report Lithuanian 30-11-2021
Patient Information leaflet Patient Information leaflet Hungarian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 04-01-2024
Public Assessment Report Public Assessment Report Hungarian 30-11-2021
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Patient Information leaflet Patient Information leaflet Portuguese 04-01-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 04-01-2024
Public Assessment Report Public Assessment Report Portuguese 30-11-2021
Patient Information leaflet Patient Information leaflet Romanian 04-01-2024
Public Assessment Report Public Assessment Report Romanian 30-11-2021
Patient Information leaflet Patient Information leaflet Slovak 04-01-2024
Public Assessment Report Public Assessment Report Slovak 30-11-2021
Patient Information leaflet Patient Information leaflet Slovenian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 04-01-2024
Public Assessment Report Public Assessment Report Slovenian 30-11-2021
Patient Information leaflet Patient Information leaflet Finnish 04-01-2024
Public Assessment Report Public Assessment Report Finnish 30-11-2021
Patient Information leaflet Patient Information leaflet Swedish 04-01-2024
Public Assessment Report Public Assessment Report Swedish 30-11-2021
Patient Information leaflet Patient Information leaflet Norwegian 04-01-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 04-01-2024
Patient Information leaflet Patient Information leaflet Icelandic 04-01-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 04-01-2024

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