Dupixent

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

dupilumab

Available from:

Sanofi Winthrop Industrie

ATC code:

D11AH05

INN (International Name):

dupilumab

Therapeutic group:

Agenti za dermatitis, isključujući kortikosteroide

Therapeutic area:

Dermatitis, Atopic; Prurigo; Esophageal Diseases; Asthma; Sinusitis

Therapeutic indications:

Atopic dermatitisAdults and adolescentsDupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. Children 6 months to 11 years of ageDupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. AsthmaAdults and adolescentsDupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (FeNO), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ICS) plus another medicinal product for maintenance treatment. Children 6 to 11 years of ageDupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (FeNO), who are inadequately controlled with medium to high dose inhaled corticosteroids (ICS) plus another medicinal product for maintenance treatment. Chronic rhinosinusitis with nasal polyposis (CRSwNP)Dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe CRSwNP for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. Prurigo Nodularis (PN)Dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (PN) who are candidates for systemic therapy. Eosinophilic esophagitis (EoE)Dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Product summary:

Revision: 30

Authorization status:

odobren

Authorization date:

2017-09-26

Patient Information leaflet

                                140
B. UPUTA O LIJEKU
141
UPUTA O LIJEKU: INFORMACIJE ZA KORISNIKA
DUPIXENT 300 MG OTOPINA ZA INJEKCIJU U NAPUNJENOJ ŠTRCALJKI
dupilumab
PAŽLJIVO PROČITAJTE CIJELU UPUTU PRIJE NEGO POČNETE PRIMJENJIVATI
OVAJ LIJEK JER SADRŽI VAMA
VAŽNE PODATKE.
-
Sačuvajte ovu uputu. Možda ćete je trebati ponovno pročitati.
-
Ako imate dodatnih pitanja, obratite se liječniku, ljekarniku ili
medicinskoj sestri.
-
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 Dupixent i za što se koristi
2.
Što morate znati prije nego počnete primjenjivati Dupixent
3.
Kako primjenjivati Dupixent
4.
Moguće nuspojave
5.
Kako čuvati Dupixent
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE DUPIXENT I ZA ŠTO SE KORISTI
ŠTO JE DUPIXENT
Dupixent sadrži djelatnu tvar dupilumab.
Dupilumab je monoklonsko protutijelo (jedna vrsta specijaliziranog
proteina) koje blokira djelovanje
proteina zvanih interleukini: IL-4 i IL-13. Oba ta proteina igraju
veliku ulogu u izazivanju znakova i
simptoma atopijskog dermatitisa, astme, kroničnog rinosinuitisa s
nosnim polipima, nodularnog
pruriga i eozinofilnog ezofagitisa.
ZA ŠTO SE DUPIXENT KORISTI
Dupixent se koristi za liječenje odraslih osoba i adolescenata u dobi
od 12 ili više godina s umjerenim
do teškim atopijskim dermatitisom, koji se još naziva i atopijskim
ekcemom. Dupixent se također
koristi za liječenje djece u dobi od 6 mjeseci do 11 godina s teškim
atopijskim dermatitisom. Dupixent
se može koristiti zajedno s lijekovima za ekcem koji se nanose na
kožu ili se može primjenjivati
samostalno.
Dupixent se također koristi zajedno s drugim lijekovima za astmu kao
terapija održavanja za tešku
astmu u odraslih, adolescenata i djece u dobi od 6 ili više g
                                
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Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Dupixent 300 mg otopina za injekciju u napunjenoj štrcaljki
Dupixent 300 mg otopina za injekciju u napunjenoj brizgalici
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Dupilumab 300 mg otopina za injekciju u napunjenoj štrcaljki
Jedna napunjena štrcaljka za jednokratnu uporabu sadrži 300 mg
dupilumaba u 2 ml otopine
(150 mg/ml).
Dupilumab 300 mg otopina za injekciju u napunjenoj brizgalici
Jedna napunjena brizgalica za jednokratnu uporabu sadrži 300 mg
dupilumaba u 2 ml otopine
(150 mg/ml).
Dupilumab je potpuno ljudsko monoklonsko protutijelo proizvedeno u
stanicama jajnika kineskog
hrčka (engl. _Chinese Hamster Ovary_, CHO) tehnologijom rekombinantne
DNA.
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Otopina za injekciju (injekcija).
Bistra do blago opalescentna, bezbojna do blijedo žuta sterilna
otopina, koja ne sadrži vidljive čestice i
čija pH vrijednost iznosi približno 5,9.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Atopijski dermatitis
_Odrasli bolesnici i adolescenti _
Dupixent je indiciran za liječenje umjerenog do teškog atopijskog
dermatitisa u odraslih bolesnika i
adolescenata u dobi od 12 ili više godina koji su kandidati za
sistemsku terapiju.
_Djeca u dobi od 6 mjeseci do 11 godina _
Dupixent je indiciran za liječenje teškog atopijskog dermatitisa u
djece u dobi od 6 mjeseci do 11
godina koja su kandidati za sistemsku terapiju.
Astma
_Odrasli bolesnici i adolescenti _
Dupixent je indiciran kao dodatak terapiji održavanja za tešku astmu
s upalom tipa 2, za koju su
karakteristične povišene razine eozinofila u krvi i/ili povišena
frakcija izdahnutog dušikova oksida
(engl. _fractional exhaled nitric oxide_, FeNO), vidjeti dio 5.1, u
odraslih bolesnika i adolescenata u
dobi od 12 ili više godina kojima bolest nije dovoljno dobro
kontrolirana visokom dozom inhalacijskih
kortikosteroida (IKS) i još jednim lijekom za terapiju održavanja.
3
_Djeca u dobi od 6 do 11 godina _
Dupixent je indiciran kao
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 10-10-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 10-10-2023
Public Assessment Report Public Assessment Report Bulgarian 23-03-2023
Patient Information leaflet Patient Information leaflet Spanish 10-10-2023
Public Assessment Report Public Assessment Report Spanish 23-03-2023
Patient Information leaflet Patient Information leaflet Czech 10-10-2023
Public Assessment Report Public Assessment Report Czech 23-03-2023
Patient Information leaflet Patient Information leaflet Danish 10-10-2023
Public Assessment Report Public Assessment Report Danish 23-03-2023
Patient Information leaflet Patient Information leaflet German 10-10-2023
Public Assessment Report Public Assessment Report German 23-03-2023
Patient Information leaflet Patient Information leaflet Estonian 10-10-2023
Public Assessment Report Public Assessment Report Estonian 23-03-2023
Patient Information leaflet Patient Information leaflet Greek 10-10-2023
Public Assessment Report Public Assessment Report Greek 23-03-2023
Patient Information leaflet Patient Information leaflet English 10-10-2023
Public Assessment Report Public Assessment Report English 23-03-2023
Patient Information leaflet Patient Information leaflet French 10-10-2023
Public Assessment Report Public Assessment Report French 23-03-2023
Patient Information leaflet Patient Information leaflet Italian 10-10-2023
Public Assessment Report Public Assessment Report Italian 23-03-2023
Patient Information leaflet Patient Information leaflet Latvian 10-10-2023
Public Assessment Report Public Assessment Report Latvian 23-03-2023
Patient Information leaflet Patient Information leaflet Lithuanian 10-10-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 10-10-2023
Public Assessment Report Public Assessment Report Lithuanian 23-03-2023
Patient Information leaflet Patient Information leaflet Hungarian 10-10-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 10-10-2023
Public Assessment Report Public Assessment Report Hungarian 23-03-2023
Patient Information leaflet Patient Information leaflet Maltese 10-10-2023
Public Assessment Report Public Assessment Report Maltese 23-03-2023
Patient Information leaflet Patient Information leaflet Dutch 10-10-2023
Public Assessment Report Public Assessment Report Dutch 23-03-2023
Patient Information leaflet Patient Information leaflet Polish 10-10-2023
Public Assessment Report Public Assessment Report Polish 23-03-2023
Patient Information leaflet Patient Information leaflet Portuguese 10-10-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 10-10-2023
Public Assessment Report Public Assessment Report Portuguese 23-03-2023
Patient Information leaflet Patient Information leaflet Romanian 10-10-2023
Public Assessment Report Public Assessment Report Romanian 23-03-2023
Patient Information leaflet Patient Information leaflet Slovak 10-10-2023
Public Assessment Report Public Assessment Report Slovak 23-03-2023
Patient Information leaflet Patient Information leaflet Slovenian 10-10-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 10-10-2023
Public Assessment Report Public Assessment Report Slovenian 23-03-2023
Patient Information leaflet Patient Information leaflet Finnish 10-10-2023
Public Assessment Report Public Assessment Report Finnish 23-03-2023
Patient Information leaflet Patient Information leaflet Swedish 10-10-2023
Public Assessment Report Public Assessment Report Swedish 23-03-2023
Patient Information leaflet Patient Information leaflet Norwegian 10-10-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 10-10-2023
Patient Information leaflet Patient Information leaflet Icelandic 10-10-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 10-10-2023

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