Taltz

Country: Unjoni Ewropea

Lingwa: Ingliż

Sors: EMA (European Medicines Agency)

Ixtrih issa

Ingredjent attiv:

ixekizumab

Disponibbli minn:

Eli Lilly and Company (Ireland) Limited

Kodiċi ATC:

L04AC

INN (Isem Internazzjonali):

ixekizumab

Grupp terapewtiku:

Immunosuppressants

Żona terapewtika:

Psoriasis

Indikazzjonijiet terapewtiċi:

Plaque psoriasisTaltz is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy.Psoriatic arthritisTaltz, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drug (DMARD) therapies.

Sommarju tal-prodott:

Revision: 17

L-istatus ta 'awtorizzazzjoni:

Authorised

Data ta 'l-awtorizzazzjoni:

2016-04-25

Fuljett ta 'informazzjoni

                                71
B. PACKAGE LEAFLET
72
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
TALTZ 80 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
ixekizumab
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
-
Keep this leaflet. You may need to read it again.
-
If you have any further questions, ask your doctor, pharmacist or
nurse.
-
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.
-
If you get any side effects, talk to your doctor, pharmacist or nurse.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Taltz is and what it is used for
2.
What you need to know before you use Taltz
3.
How to use Taltz
4.
Possible side effects
5.
How to store Taltz
6.
Contents of the pack and other information
1.
WHAT TALTZ IS AND WHAT IT IS USED FOR
Taltz contains the active substance ixekizumab.
Taltz is intended for the treatment of the inflammatory diseases
described below:
•
Plaque psoriasis in adults
•
Plaque psoriasis in children from the age of 6 and with a body weight
of at least 25 kg
_ _
and in
adolescents
•
Psoriatic arthritis in adults
_ _
•
Radiographic Axial Spondyloarthritis in adults
_ _
•
Non-radiographic Axial
_S_
pondyloarthritis in adults
_ _
Ixekizumab belongs to a group of medicines called interleukin (IL)
inhibitors. This medicine
works by blocking the activity of a protein called IL-17A, which
promotes psoriasis and
inflammatory disease of the joints and the spine.
Plaque psoriasis
Taltz is used to treat a skin condition called “plaque psoriasis”
in adults and in children from the age
of 6 years and with a body weight of at least 25 kg
_ _
and in adolescents with moderate to severe
disease. Taltz reduces the signs and symptoms of the disease.
Using Taltz will benefit you by improvements of skin clearance and
reducing your symptoms
such as scaling, itching and pain.
Psoriatic arth
                                
                                Aqra d-dokument sħiħ
                                
                            

Karatteristiċi tal-prodott

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Taltz 80 mg solution for injection in pre-filled syringe
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each pre-filled syringe contains 80 mg ixekizumab in 1 ml.
Ixekizumab is produced in CHO cells by recombinant DNA technology.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection (injection).
The solution is clear and colourless to slightly yellow.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Plaque psoriasis
Taltz is indicated for the treatment of moderate to severe plaque
psoriasis in adults who are candidates
for systemic therapy.
Paediatric plaque psoriasis
Taltz is indicated for the treatment of moderate to severe plaque
psoriasis in children from the age
of 6 years and with a body weight of at least 25 kg and adolescents
who are candidates for
systemic therapy.
Psoriatic arthritis
Taltz, alone or in combination with methotrexate, is indicated for the
treatment of active psoriatic
arthritis in adult patients who have responded inadequately to, or who
are intolerant to one or more
disease-modifying anti-rheumatic drug (DMARD) therapies (see section
5.1).
Axial spondyloarthritis
_ _
_Ankylosing spondylitis (radiographic axial spondyloarthritis) _
Taltz is indicated for the treatment of adult patients with active
ankylosing spondylitis who have
responded inadequately to conventional therapy.
_ _
_Non-radiographic axial spondyloarthritis _
Taltz is indicated for the treatment of adult patients 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 to nonsteroidal
anti-inflammatory drugs (NSAIDs).
3
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
This medicinal product is intended for use under the guidance and
supervision of a physician
experienced in the diagnosis and treatment of conditions for which it
is indicated.
Posology
_Plaque p
                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Bulgaru 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Bulgaru 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Spanjol 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Spanjol 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ċek 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ċek 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Daniż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Daniż 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ġermaniż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ġermaniż 22-02-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ġermaniż 02-05-2016
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Estonjan 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Estonjan 22-02-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Estonjan 02-05-2016
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Grieg 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Grieg 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Franċiż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 22-02-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Franċiż 02-05-2016
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Taljan 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Taljan 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Latvjan 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Latvjan 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Litwanjan 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Litwanjan 22-02-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Litwanjan 02-05-2016
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ungeriż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ungeriż 22-02-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ungeriż 02-05-2016
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Malti 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Malti 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Olandiż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Olandiż 22-02-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Olandiż 02-05-2016
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Pollakk 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Pollakk 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Portugiż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Portugiż 22-02-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Portugiż 02-05-2016
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Rumen 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Rumen 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Slovakk 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Slovakk 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Sloven 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Sloven 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Finlandiż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Finlandiż 22-02-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Finlandiż 02-05-2016
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Svediż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Svediż 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Norveġiż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Norveġiż 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Iżlandiż 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Iżlandiż 22-02-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Kroat 22-02-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Kroat 22-02-2023

Fittex twissijiet relatati ma 'dan il-prodott

Ara l-istorja tad-dokumenti