Taltz

Pays: Union européenne

Langue: anglais

Source: EMA (European Medicines Agency)

Achète-le

Ingrédients actifs:

ixekizumab

Disponible depuis:

Eli Lilly and Company (Ireland) Limited

Code ATC:

L04AC

DCI (Dénomination commune internationale):

ixekizumab

Groupe thérapeutique:

Immunosuppressants

Domaine thérapeutique:

Psoriasis

indications thérapeutiques:

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.

Descriptif du produit:

Revision: 17

Statut de autorisation:

Authorised

Date de l'autorisation:

2016-04-25

Notice patient

                                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
                                
                                Lire le document complet
                                
                            

Résumé des caractéristiques du produit

                                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
                                
                                Lire le document complet
                                
                            

Documents dans d'autres langues

Notice patient Notice patient bulgare 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation bulgare 02-05-2016
Notice patient Notice patient espagnol 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation espagnol 02-05-2016
Notice patient Notice patient tchèque 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation tchèque 02-05-2016
Notice patient Notice patient danois 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation danois 02-05-2016
Notice patient Notice patient allemand 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation allemand 02-05-2016
Notice patient Notice patient estonien 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation estonien 02-05-2016
Notice patient Notice patient grec 22-02-2023
Notice patient Notice patient français 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation français 02-05-2016
Notice patient Notice patient italien 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation italien 02-05-2016
Notice patient Notice patient letton 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation letton 02-05-2016
Notice patient Notice patient lituanien 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation lituanien 02-05-2016
Notice patient Notice patient hongrois 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation hongrois 02-05-2016
Notice patient Notice patient maltais 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation maltais 02-05-2016
Notice patient Notice patient néerlandais 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation néerlandais 02-05-2016
Notice patient Notice patient polonais 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation polonais 02-05-2016
Notice patient Notice patient portugais 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation portugais 02-05-2016
Notice patient Notice patient roumain 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation roumain 02-05-2016
Notice patient Notice patient slovaque 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation slovaque 02-05-2016
Notice patient Notice patient slovène 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation slovène 02-05-2016
Notice patient Notice patient finnois 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation finnois 02-05-2016
Notice patient Notice patient suédois 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation suédois 02-05-2016
Notice patient Notice patient norvégien 22-02-2023
Notice patient Notice patient islandais 22-02-2023
Notice patient Notice patient croate 22-02-2023
Rapport public d'évaluation Rapport public d'évaluation croate 02-05-2016

Rechercher des alertes liées à ce produit

Afficher l'historique des documents