Otezla

Maa: Euroopan unioni

Kieli: englanti

Lähde: EMA (European Medicines Agency)

Osta se nyt

Pakkausseloste Pakkausseloste (PIL)
21-07-2022
Valmisteyhteenveto Valmisteyhteenveto (SPC)
21-07-2022

Aktiivinen ainesosa:

apremilast

Saatavilla:

Amgen Europe BV

ATC-koodi:

L04AA32

INN (Kansainvälinen yleisnimi):

apremilast

Terapeuttinen ryhmä:

Immunosuppressants

Terapeuttinen alue:

Arthritis, Psoriatic; Psoriasis

Käyttöaiheet:

Psoriatic arthritisOtezla, alone or in combination with Disease Modifying Antirheumatic Drugs (DMARDs), is indicated for the treatment of active psoriatic arthritis (PsA) in adult patients who have had an inadequate response or who have been intolerant to a prior DMARD therapy.PsoriasisOtezla is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who failed to respond to or who have a contraindication to, or are intolerant to other systemic therapy including cyclosporine, methotrexate or psoralen and ultraviolet-A light (PUVA).

Tuoteyhteenveto:

Revision: 21

Valtuutuksen tilan:

Authorised

Valtuutus päivämäärä:

2015-01-15

Pakkausseloste

                                33
B. PACKAGE LEAFLET
34
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
OTEZLA 10 MG FILM-COATED TABLETS
OTEZLA 20 MG FILM-COATED TABLETS
OTEZLA 30 MG FILM-COATED TABLETS
apremilast
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING 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 Otezla is and what it is used for
2.
What you need to know before you take Otezla
3.
How to take Otezla
4.
Possible side effects
5.
How to store Otezla
6.
Contents of the pack and other information
1.
WHAT OTEZLA IS AND WHAT IT IS USED FOR
WHAT OTEZLA IS
Otezla contains the active substance ‘apremilast’. This belongs to
a group of medicines called
phosphodiesterase 4 inhibitors, which help to reduce inflammation.
WHAT OTEZLA IS USED FOR
Otezla is used to treat adults with the following conditions:
•
ACTIVE PSORIATIC ARTHRITIS -
if you cannot use another type of medicine called
‘Disease-Modifying Antirheumatic Drugs’ (DMARDs) or when you have
tried one of these
medicines and it did not work.
•
MODERATE TO SEVERE CHRONIC PLAQUE PSORIASIS
-
if you cannot use one of the following
treatments or when you have tried one of these treatments and it did
not work:
-
phototherapy - a treatment where certain areas of skin are exposed to
ultraviolet light
-
systemic therapy - a treatment that affects the entire body rather
than just one local area,
such as ‘ciclosporin’, ‘methotrexate’ or ‘psoralen ’.
•
BEHÇET’S DISEASE (BD)
- to treat the mouth ulcers which is a common problem for people with
this illness.
WHAT PSORIATIC ARTHRITIS IS
Psoriati
                                
                                Lue koko asiakirja
                                
                            

Valmisteyhteenveto

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Otezla 10 mg film-coated tablets
Otezla 20 mg film-coated tablets
Otezla 30 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Otezla 10 mg film-coated tablets
Each film-coated tablet contains 10 mg of apremilast.
_Excipient(s) with known effect _
Each film-coated tablet contains 57 mg of lactose (as lactose
monohydrate).
Otezla 20 mg film-coated tablets
Each film-coated tablet contains 20 mg of apremilast.
_ _
_Excipient(s) with known effect _
Each film-coated tablet contains 114 mg of lactose (as lactose
monohydrate).
Otezla 30 mg film-coated tablets
Each film-coated tablet contains 30 mg of apremilast.
_ _
_Excipient(s) with known effect _
Each film-coated tablet contains 171 mg of lactose (as lactose
monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Otezla 10 mg film-coated tablets
Pink, diamond shaped 10 mg film-coated tablet of 8 mm length with
“APR” engraved on one side and
“10” on the opposite side.
Otezla 20 mg film-coated tablets
Brown, diamond shaped 20 mg film-coated tablet of 10 mm length with
“APR” engraved on one side
and “20” on the opposite side.
Otezla 30 mg film-coated tablets
Beige, diamond shaped 30 mg film-coated tablet of 12 mm length with
“APR” engraved on one side
and “30” on the opposite side.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Psoriatic arthritis
Otezla, alone or in combination with Disease Modifying Antirheumatic
Drugs (DMARDs), is
indicated for the treatment of active psoriatic arthritis (PsA) in
adult patients who have had an
inadequate response or who have been intolerant to a prior DMARD
therapy (see section 5.1).
Psoriasis
Otezla is indicated for the treatment of moderate to severe chronic
plaque psoriasis in adult patients
who failed to respond to or who have a contraindication to, or are
intolerant to other systemic therapy
including cyclosporine, methotrexate or psoralen and u
                                
                                Lue koko asiakirja
                                
                            

Asiakirjat muilla kielillä

Pakkausseloste Pakkausseloste bulgaria 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto bulgaria 21-07-2022
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta bulgaria 05-03-2024
Pakkausseloste Pakkausseloste espanja 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto espanja 21-07-2022
Pakkausseloste Pakkausseloste tšekki 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto tšekki 21-07-2022
Pakkausseloste Pakkausseloste tanska 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto tanska 21-07-2022
Pakkausseloste Pakkausseloste saksa 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto saksa 21-07-2022
Pakkausseloste Pakkausseloste viro 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto viro 21-07-2022
Pakkausseloste Pakkausseloste kreikka 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto kreikka 21-07-2022
Pakkausseloste Pakkausseloste ranska 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto ranska 21-07-2022
Pakkausseloste Pakkausseloste italia 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto italia 21-07-2022
Pakkausseloste Pakkausseloste latvia 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto latvia 21-07-2022
Pakkausseloste Pakkausseloste liettua 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto liettua 21-07-2022
Pakkausseloste Pakkausseloste unkari 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto unkari 21-07-2022
Pakkausseloste Pakkausseloste malta 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto malta 21-07-2022
Pakkausseloste Pakkausseloste hollanti 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto hollanti 21-07-2022
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta hollanti 05-03-2024
Pakkausseloste Pakkausseloste puola 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto puola 21-07-2022
Pakkausseloste Pakkausseloste portugali 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto portugali 21-07-2022
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta portugali 05-03-2024
Pakkausseloste Pakkausseloste romania 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto romania 21-07-2022
Pakkausseloste Pakkausseloste slovakki 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto slovakki 21-07-2022
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta slovakki 05-03-2024
Pakkausseloste Pakkausseloste sloveeni 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto sloveeni 21-07-2022
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta sloveeni 05-03-2024
Pakkausseloste Pakkausseloste suomi 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto suomi 21-07-2022
Pakkausseloste Pakkausseloste ruotsi 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto ruotsi 21-07-2022
Pakkausseloste Pakkausseloste norja 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto norja 21-07-2022
Pakkausseloste Pakkausseloste islanti 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto islanti 21-07-2022
Pakkausseloste Pakkausseloste kroatia 21-07-2022
Valmisteyhteenveto Valmisteyhteenveto kroatia 21-07-2022

Etsi tähän tuotteeseen liittyviä ilmoituksia

Näytä asiakirjojen historia