Skyrizi

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

Risankizumab

Available from:

AbbVie Deutschland GmbH & Co. KG

ATC code:

L04AC18

INN (International Name):

risankizumab

Therapeutic group:

imunosupresivi

Therapeutic area:

Psoriasis; Arthritis, Psoriatic

Therapeutic indications:

Plaque PsoriasisSkyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. Psoriatic ArthritisSkyrizi, alone or in combination with methotrexate (MTX), is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (DMARDs). Crohn's diseaseSkyrizi is indicated for the treatment of adult patients with moderately to severely active Crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.

Product summary:

Revision: 18

Authorization status:

odobren

Authorization date:

2019-04-26

Patient Information leaflet

                                82
B. UPUTA O LIJEKU
83
UPUTA O LIJEKU: INFORMACIJE ZA BOLESNIKA
SKYRIZI 150 MG OTOPINA ZA INJEKCIJU U NAPUNJENOJ BRIZGALICI
risankizumab
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 Skyrizi i za što se koristi
2.
Što morate znati prije nego počnete primjenjivati Skyrizi
3.
Kako primjenjivati Skyrizi
4.
Moguće nuspojave
5.
Kako čuvati Skyrizi
6.
Sadržaj pakiranja i druge informacije
7.
Upute za uporabu
1.
ŠTO JE SKYRIZI I ZA ŠTO SE KORISTI
Skyrizi sadrži djelatnu tvar risankizumab.
Skyrizi se koristi za liječenje sljedećih upalnih bolesti:
•
plak psorijaze
•
psorijatičnog artritisa
KAKO SKYRIZI DJELUJE
Ovaj lijek djeluje tako da u tijelu zaustavlja djelovanje proteina pod
nazivom „IL-23“, koji uzrokuje
upalu.
Plak psorijaza
Skyrizi se koristi za liječenje odraslih osoba s umjerenom do teškom
plak psorijazom. Skyrizi
smanjuje upalu i stoga može pomoći ublažiti simptome plak
psorijaze, kao što su žarenje, svrbež, bol,
crvenilo i ljuskanje kože.
Psorijatični artritis
Skyrizi se koristi za liječenje odraslih osoba s psorijatičnim
artritisom. Psorijatični artritis je bolest
koja uzrokuje upalu zglobova i psorijazu. Ako imate aktivan
psorijatični artritis, možda ćete najprije
primati druge lijekove. Ako ti lijekovi ne budu dovoljno dobro
djelovali, primit ćete Skyrizi, bilo
samostalno ili u kombinaciji s drugim lijekovima za liječenje
psorijatičnog artritisa.
Skyrizi smanjuje upalu i stog
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Skyrizi 150 mg otopina za injekciju u napunjenoj brizgalici
Skyrizi 150 mg otopina za injekciju u napunjenoj štrcaljki
Skyrizi 75 mg otopina za injekciju u napunjenoj štrcaljki
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Skyrizi 150 mg otopina za injekciju u napunjenoj brizgalici
Jedna napunjena brizgalica sadrži 150 mg risankizumaba u 1 ml
otopine.
Skyrizi 150 mg otopina za injekciju u napunjenoj štrcaljki
Jedna napunjena štrcaljka sadrži 150 mg risankizumaba u 1 ml
otopine.
Skyrizi 75 mg otopina za injekciju u napunjenoj štrcaljki
Jedna napunjena štrcaljka sadrži 75 mg risankizumaba u 0,83 ml
otopine.
Risankizumab je humanizirano imunoglobulinsko G1 (IgG1) monoklonsko
protutijelo proizvedeno u
stanicama jajnika kineskog hrčka tehnologijom rekombinantne DNA.
_Pomoćne tvari s poznatim učinkom (samo za 75 mg otopinu za
injekciju) _
Ovaj lijek sadrži 68,0 mg sorbitola po dozi od 150 mg.
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Otopina za injekciju (injekcija)
Skyrizi 150 mg otopina za injekciju u napunjenoj brizgalici i
napunjenoj štrcaljki
Otopina je bezbojna do žuta te bistra do blago opalescentna.
Skyrizi 75 mg otopina za injekciju u napunjenoj štrcaljki
Otopina je bezbojna do svjetložuta te bistra do blago opalescentna.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Plak psorijaza
Skyrizi je indiciran za liječenje umjerene do teške plak psorijaze u
odraslih koji su kandidati za
sistemsku terapiju.
Psorijatični artritis
Skyrizi je u monoterapiji ili u kombinaciji s metotreksatom (MTX)
indiciran za liječenje aktivnog
psorijatičnog artritisa u odraslih koji nisu dovoljno dobro
odgovorili na jedan ili više antireumatskih
3
lijekova koji modificiraju tijek bolesti (engl.
_disease-modifying anti-rheumatic drug_
, DMARD) ili koji
ne podnose te lijekove.
4.2
DOZIRANJE I NAČIN PRIMJENE
Ovaj je lijek namijenjen za primjenu pod vodstvom i nadzorom
liječnika koji ima iskustva u
postavljanju dijagnoze i liječen
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 15-03-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 15-03-2024
Public Assessment Report Public Assessment Report Bulgarian 08-12-2022
Patient Information leaflet Patient Information leaflet Spanish 15-03-2024
Public Assessment Report Public Assessment Report Spanish 08-12-2022
Patient Information leaflet Patient Information leaflet Czech 15-03-2024
Public Assessment Report Public Assessment Report Czech 08-12-2022
Patient Information leaflet Patient Information leaflet Danish 15-03-2024
Public Assessment Report Public Assessment Report Danish 08-12-2022
Patient Information leaflet Patient Information leaflet German 15-03-2024
Public Assessment Report Public Assessment Report German 08-12-2022
Patient Information leaflet Patient Information leaflet Estonian 15-03-2024
Public Assessment Report Public Assessment Report Estonian 08-12-2022
Patient Information leaflet Patient Information leaflet Greek 15-03-2024
Public Assessment Report Public Assessment Report Greek 08-12-2022
Patient Information leaflet Patient Information leaflet English 15-03-2024
Public Assessment Report Public Assessment Report English 08-12-2022
Patient Information leaflet Patient Information leaflet French 15-03-2024
Public Assessment Report Public Assessment Report French 08-12-2022
Patient Information leaflet Patient Information leaflet Italian 15-03-2024
Public Assessment Report Public Assessment Report Italian 08-12-2022
Patient Information leaflet Patient Information leaflet Latvian 15-03-2024
Public Assessment Report Public Assessment Report Latvian 08-12-2022
Patient Information leaflet Patient Information leaflet Lithuanian 15-03-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 15-03-2024
Public Assessment Report Public Assessment Report Lithuanian 08-12-2022
Patient Information leaflet Patient Information leaflet Hungarian 15-03-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 15-03-2024
Public Assessment Report Public Assessment Report Hungarian 08-12-2022
Patient Information leaflet Patient Information leaflet Maltese 15-03-2024
Public Assessment Report Public Assessment Report Maltese 08-12-2022
Patient Information leaflet Patient Information leaflet Dutch 15-03-2024
Public Assessment Report Public Assessment Report Dutch 08-12-2022
Patient Information leaflet Patient Information leaflet Polish 15-03-2024
Public Assessment Report Public Assessment Report Polish 08-12-2022
Patient Information leaflet Patient Information leaflet Portuguese 15-03-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 15-03-2024
Public Assessment Report Public Assessment Report Portuguese 08-12-2022
Patient Information leaflet Patient Information leaflet Romanian 15-03-2024
Public Assessment Report Public Assessment Report Romanian 08-12-2022
Patient Information leaflet Patient Information leaflet Slovak 15-03-2024
Public Assessment Report Public Assessment Report Slovak 08-12-2022
Patient Information leaflet Patient Information leaflet Slovenian 15-03-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 15-03-2024
Public Assessment Report Public Assessment Report Slovenian 08-12-2022
Patient Information leaflet Patient Information leaflet Finnish 15-03-2024
Public Assessment Report Public Assessment Report Finnish 08-12-2022
Patient Information leaflet Patient Information leaflet Swedish 15-03-2024
Public Assessment Report Public Assessment Report Swedish 08-12-2022
Patient Information leaflet Patient Information leaflet Norwegian 15-03-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 15-03-2024
Patient Information leaflet Patient Information leaflet Icelandic 15-03-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 15-03-2024

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