Xeljanz

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

Тофацитиниб

Available from:

Pfizer Europe MA EEIG

ATC code:

L04AA29

INN (International Name):

tofacitinib

Therapeutic group:

Имуносупресори

Therapeutic area:

Артрит, ревматоиден

Therapeutic indications:

Rheumatoid arthritisTofacitinib in combination with methotrexate (MTX) is indicated for the treatment of moderate to severe active rheumatoid arthritis (RA) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (DMARDs) (see section 5. Tofacitinib can be given as monotherapy in case of intolerance to MTX or when treatment with MTX is inappropriate (see sections 4. 4 и 4. Psoriatic arthritisTofacitinib in combination with MTX 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 disease modifying antirheumatic drug (DMARD) therapy (see section 5. Ulcerative colitisTofacitinib is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (UC) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent (see section 5. Tofacitinib is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (rheumatoid factor positive [RF+] or negative [RF-] polyarthritis and extended oligoarthritis), and juvenile psoriatic arthritis (PsA) in patients 2 years of age and older, who have responded inadequately to previous therapy with disease modifying antirheumatic drugs (DMARDs). Tofacitinib can be given in combination with methotrexate (MTX) or as monotherapy in case of intolerance to MTX or where continued treatment with MTX is inappropriate. Ankylosing spondylitisTofacitinib is indicated for the treatment of adult patients with active ankylosing spondylitis (AS) who have responded inadequately to conventional therapy.

Product summary:

Revision: 28

Authorization status:

упълномощен

Authorization date:

2017-03-22

Patient Information leaflet

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
XELJANZ 5 mg филмирани таблетки
XELJANZ 10 mg филмирани таблетки
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
XELJANZ 5 mg филмирани таблетки
Всяка филмирана таблетка съдържа
тофацитинибов цитрат, еквивалентен на
5 mg тофацитиниб
(tofacitinib).
_Помощно вещество с известно действие_
Всяка филмирана таблетка съдържа 59,44 mg
лактоза.
XELJANZ 10 mg филмирани таблетки
Всяка филмирана таблетка съдържа
тофацитинибов цитрат, еквивалентен на
10 mg
тофацитиниб (tofacitinib).
_Помощно вещество с известно действие_
Всяка филмирана таблетка съдържа 118,88
mg лактоза.
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Филмирана таблетка (таблетка)
XELJANZ 5 mg филмирани таблетки
Бяла, кръгла таблетка с диаметър 7,9 mm и
вдлъбнато релефно означение „Pfizer“ от
едната
страна и „JKI 5“ от другата.
XELJANZ 10 mg филмирани таблетки
Синя, кръгла таблетка с диаметър 9,5 mm и
вдлъбнато релефно означение „Pfizer“ от
едната
страна и „JKI 10“ от другата.
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Ревматоиден артрит
Тофацитиниб в комбинация с
метотрексат (MTX) е показан за лечение
на умерено тежък до
тежъ
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
XELJANZ 5 mg филмирани таблетки
XELJANZ 10 mg филмирани таблетки
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
XELJANZ 5 mg филмирани таблетки
Всяка филмирана таблетка съдържа
тофацитинибов цитрат, еквивалентен на
5 mg тофацитиниб
(tofacitinib).
_Помощно вещество с известно действие_
Всяка филмирана таблетка съдържа 59,44 mg
лактоза.
XELJANZ 10 mg филмирани таблетки
Всяка филмирана таблетка съдържа
тофацитинибов цитрат, еквивалентен на
10 mg
тофацитиниб (tofacitinib).
_Помощно вещество с известно действие_
Всяка филмирана таблетка съдържа 118,88
mg лактоза.
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Филмирана таблетка (таблетка)
XELJANZ 5 mg филмирани таблетки
Бяла, кръгла таблетка с диаметър 7,9 mm и
вдлъбнато релефно означение „Pfizer“ от
едната
страна и „JKI 5“ от другата.
XELJANZ 10 mg филмирани таблетки
Синя, кръгла таблетка с диаметър 9,5 mm и
вдлъбнато релефно означение „Pfizer“ от
едната
страна и „JKI 10“ от другата.
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Ревматоиден артрит
Тофацитиниб в комбинация с
метотрексат (MTX) е показан за лечение
на умерено тежък до
тежъ
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 07-12-2023
Public Assessment Report Public Assessment Report Spanish 12-06-2023
Patient Information leaflet Patient Information leaflet Czech 07-12-2023
Public Assessment Report Public Assessment Report Czech 12-06-2023
Patient Information leaflet Patient Information leaflet Danish 07-12-2023
Public Assessment Report Public Assessment Report Danish 12-06-2023
Patient Information leaflet Patient Information leaflet German 07-12-2023
Public Assessment Report Public Assessment Report German 12-06-2023
Patient Information leaflet Patient Information leaflet Estonian 07-12-2023
Public Assessment Report Public Assessment Report Estonian 12-06-2023
Patient Information leaflet Patient Information leaflet Greek 07-12-2023
Public Assessment Report Public Assessment Report Greek 12-06-2023
Patient Information leaflet Patient Information leaflet English 07-12-2023
Public Assessment Report Public Assessment Report English 12-06-2023
Patient Information leaflet Patient Information leaflet French 07-12-2023
Public Assessment Report Public Assessment Report French 12-06-2023
Patient Information leaflet Patient Information leaflet Italian 07-12-2023
Public Assessment Report Public Assessment Report Italian 12-06-2023
Patient Information leaflet Patient Information leaflet Latvian 07-12-2023
Public Assessment Report Public Assessment Report Latvian 12-06-2023
Patient Information leaflet Patient Information leaflet Lithuanian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 07-12-2023
Public Assessment Report Public Assessment Report Lithuanian 12-06-2023
Patient Information leaflet Patient Information leaflet Hungarian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 07-12-2023
Public Assessment Report Public Assessment Report Hungarian 12-06-2023
Patient Information leaflet Patient Information leaflet Maltese 07-12-2023
Public Assessment Report Public Assessment Report Maltese 12-06-2023
Patient Information leaflet Patient Information leaflet Dutch 07-12-2023
Public Assessment Report Public Assessment Report Dutch 12-06-2023
Patient Information leaflet Patient Information leaflet Polish 07-12-2023
Public Assessment Report Public Assessment Report Polish 12-06-2023
Patient Information leaflet Patient Information leaflet Portuguese 07-12-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 07-12-2023
Public Assessment Report Public Assessment Report Portuguese 12-06-2023
Patient Information leaflet Patient Information leaflet Romanian 07-12-2023
Public Assessment Report Public Assessment Report Romanian 12-06-2023
Patient Information leaflet Patient Information leaflet Slovak 07-12-2023
Public Assessment Report Public Assessment Report Slovak 12-06-2023
Patient Information leaflet Patient Information leaflet Slovenian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 07-12-2023
Public Assessment Report Public Assessment Report Slovenian 12-06-2023
Patient Information leaflet Patient Information leaflet Finnish 07-12-2023
Public Assessment Report Public Assessment Report Finnish 12-06-2023
Patient Information leaflet Patient Information leaflet Swedish 07-12-2023
Public Assessment Report Public Assessment Report Swedish 12-06-2023
Patient Information leaflet Patient Information leaflet Norwegian 07-12-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 07-12-2023
Patient Information leaflet Patient Information leaflet Icelandic 07-12-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 07-12-2023
Patient Information leaflet Patient Information leaflet Croatian 07-12-2023
Public Assessment Report Public Assessment Report Croatian 12-06-2023

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