Bimzelx

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

Bimekizumab

Available from:

UCB Pharma S.A.  

ATC code:

L04AC

INN (International Name):

bimekizumab

Therapeutic group:

imunosupresivi

Therapeutic area:

Psorijaza

Therapeutic indications:

Plaque psoriasisBimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. Psoriatic arthritisBimzelx, alone or in combination with methotrexate, 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). Axial spondyloarthritisNon-radiographic axial spondyloarthritis (nr-axSpA)Bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated C-reactive protein (CRP) and/or magnetic resonance imaging (MRI) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (NSAIDs). Ankylosing spondylitis (AS, radiographic axial spondyloarthritis)Bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Product summary:

Revision: 5

Authorization status:

odobren

Authorization date:

2021-08-20

Patient Information leaflet

                                50
B. UPUTA O LIJEKU
51
UPUTA O LIJEKU: INFORMACIJE ZA KORISNIKA
BIMZELX 160 MG OTOPINA ZA INJEKCIJU U NAPUNJENOJ ŠTRCALJKI
bimekizumab
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 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 Bimzelx i za što se koristi
2.
Što morate znati prije nego počnete primjenjivati Bimzelx
3.
Kako primjenjivati Bimzelx
4.
Moguće nuspojave
5.
Kako čuvati Bimzelx
6.
Sadržaj pakiranja i druge informacije
Upute za uporabu
1.
ŠTO JE BIMZELX I ZA ŠTO SE KORISTI
ŠTO JE BIMZELX
Bimzelx sadrži djelatnu tvar bimekizumab.
ZA ŠTO SE BIMZELX KORISTI
Bimzelx se koristi za liječenje sljedećih upalnih bolesti:
•
plak psorijaze
•
psorijatičnog artritisa
•
aksijalnog spondiloartritisa, uključujući neradiografski aksijalni
spondiloartritis i ankilozantni
spondilitis (radiografski aksijalni spondiloartritis)
Plak psorijaza
Bimzelx se koristi u odraslih za liječenje kožne bolesti koja se
naziva plak psorijaza. Bimzelx
smanjuje simptome, uključujući bol, svrbež i ljuštenje kože.
Psorijatični artritis
Bimzelx se koristi za liječenje odraslih sa psorijatičnim
artritisom. Psorijatični artritis je bolest koja
uzrokuje upalu zglobova, često praćenu plak psorijazom. Ako imate
aktivni psorijatični artritis, možda
ćete
                                
                                Read the complete document
                                
                            

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
Bimzelx 160 mg otopina za injekciju u napunjenoj štrcaljki
Bimzelx 160 mg otopina za injekciju u napunjenoj brizgalici
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Bimzelx 160 mg otopina za injekciju u napunjenoj štrcaljki
Jedna napunjena štrcaljka sadrži 160 mg bimekizumaba u 1 ml.
Bimzelx 160 mg otopina za injekciju u napunjenoj brizgalici
Jedna napunjena brizgalica sadrži 160 mg bimekizumaba u 1 ml.
Bimekizumab je humanizirano monoklonsko IgG1 antitijelo proizvedeno u
genetski modificiranoj
staničnoj liniji jajnika kineskog hrčka (eng. _Chinese hamster
ovary, _CHO) tehnologijom
rekombinantne DNA.
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Otopina za injekciju (injekcija)
Otopina je bistra do blago opalescentna, bezbojna do svijetlo
smećkastožuta.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
PLAK PSORIJAZA
Bimzelx je indiciran za liječenje umjerene do teške plak psorijaze u
odraslih koji su kandidati za
sistemsku terapiju.
PSORIJATIČNI ARTRITIS
Bimzelx, sam ili u kombinaciji s metotreksatom, indiciran je za
liječenje aktivnog psorijatičnog
artritisa u odraslih koji su imali neodgovarajući odgovor ili koji
nisu podnosili jedan ili više
antireumatskih lijekova koji modificiraju tijek bolesti (engl.
_disease-modifying antirheumatic drugs_,
DMARD).
AKSIJALNI SPONDILOARTRITIS
_ _
_Neradiografski aksijalni spondiloartritis (nr-axSpA)_
Bimzelx je indiciran za liječenje odraslih osoba s aktivnim
neradiografskim aksijalnim
spondiloartritisom s objektivnim znakovima upale na koje ukazuju
povišene razine C-reaktivnog
3
proteina (CRP) i/ili magnetska rezonancija (MR), a koji nisu postigli
adekvatan odgovor ili ne
podnose nesteroidne protuupalne lijekove (NSAIL).
_Ankilozantni sp
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 13-11-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 13-11-2023
Public Assessment Report Public Assessment Report Bulgarian 03-12-2023
Patient Information leaflet Patient Information leaflet Spanish 13-11-2023
Public Assessment Report Public Assessment Report Spanish 03-12-2023
Patient Information leaflet Patient Information leaflet Czech 13-11-2023
Public Assessment Report Public Assessment Report Czech 03-12-2023
Patient Information leaflet Patient Information leaflet Danish 13-11-2023
Public Assessment Report Public Assessment Report Danish 03-12-2023
Patient Information leaflet Patient Information leaflet German 13-11-2023
Public Assessment Report Public Assessment Report German 03-12-2023
Patient Information leaflet Patient Information leaflet Estonian 13-11-2023
Public Assessment Report Public Assessment Report Estonian 03-12-2023
Patient Information leaflet Patient Information leaflet Greek 13-11-2023
Public Assessment Report Public Assessment Report Greek 03-12-2023
Patient Information leaflet Patient Information leaflet English 13-11-2023
Public Assessment Report Public Assessment Report English 15-06-2023
Patient Information leaflet Patient Information leaflet French 13-11-2023
Public Assessment Report Public Assessment Report French 03-12-2023
Patient Information leaflet Patient Information leaflet Italian 13-11-2023
Public Assessment Report Public Assessment Report Italian 03-12-2023
Patient Information leaflet Patient Information leaflet Latvian 13-11-2023
Public Assessment Report Public Assessment Report Latvian 03-12-2023
Patient Information leaflet Patient Information leaflet Lithuanian 13-11-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 13-11-2023
Public Assessment Report Public Assessment Report Lithuanian 03-12-2023
Patient Information leaflet Patient Information leaflet Hungarian 13-11-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 13-11-2023
Public Assessment Report Public Assessment Report Hungarian 03-12-2023
Patient Information leaflet Patient Information leaflet Maltese 13-11-2023
Public Assessment Report Public Assessment Report Maltese 03-12-2023
Patient Information leaflet Patient Information leaflet Dutch 13-11-2023
Public Assessment Report Public Assessment Report Dutch 03-12-2023
Patient Information leaflet Patient Information leaflet Polish 13-11-2023
Public Assessment Report Public Assessment Report Polish 03-12-2023
Patient Information leaflet Patient Information leaflet Portuguese 13-11-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 13-11-2023
Public Assessment Report Public Assessment Report Portuguese 03-12-2023
Patient Information leaflet Patient Information leaflet Romanian 13-11-2023
Public Assessment Report Public Assessment Report Romanian 03-12-2023
Patient Information leaflet Patient Information leaflet Slovak 13-11-2023
Public Assessment Report Public Assessment Report Slovak 03-12-2023
Patient Information leaflet Patient Information leaflet Slovenian 13-11-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 13-11-2023
Public Assessment Report Public Assessment Report Slovenian 03-12-2023
Patient Information leaflet Patient Information leaflet Finnish 13-11-2023
Public Assessment Report Public Assessment Report Finnish 03-12-2023
Patient Information leaflet Patient Information leaflet Swedish 13-11-2023
Public Assessment Report Public Assessment Report Swedish 03-12-2023
Patient Information leaflet Patient Information leaflet Norwegian 13-11-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 13-11-2023
Patient Information leaflet Patient Information leaflet Icelandic 13-11-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 13-11-2023

Search alerts related to this product

View documents history