Всичко за лекарството

Nepexto

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  • Режимът на отпускане не е посочен
  • Онкологични и имуномодулиращи лекарства
Активно вещество
Etanercept
Производител
Biosimilar Collaborations Ireland Limited

Цитирано от официалния източник. Все още не е прегледано от Mediclarum — листовката в опаковката е меродавна.

За какво се използва

  • Rheumatoid arthritis Nepexto in combination with methotrexate is indicated for the treatment of moderate to severe active rheumatoid arthritis in adults when the response to disease-modifying antirheumatic drugs, including methotrexate (unless contraindicated), has been inadequate. Nepexto can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate.  Nepexto is also indicated in the treatment of severe, active and progressive rheumatoid arthritis in adults not previously treated with methotrexate. Nepexto, alone or in combination with methotrexate, has been shown to reduce the rate of progression of joint damage as measured by X-ray and to improve physical function. Juvenile idiopathic arthritis Treatment of polyarthritis (rheumatoid factor positive or negative) and extended oligoarthritis in children and adolescents from the age of 2 years who have had an inadequate response to, or who have proved intolerant of, methotrexate. Treatment of psoriatic arthritis in adolescents from the age of 12 years who have had an inadequate response to, or who have proved intolerant of, methotrexate. Treatment of enthesitis-related arthritis in adolescents from the age of 12 years who have had an inadequate response to, or who have proved intolerant of, conventional therapy. Etanercept has not been studied in children aged less than 2 years. Psoriatic arthritis Treatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying antirheumatic drug therapy has been inadequate. Etanercept has been shown to improve physical function in patients with psoriatic arthritis, and to reduce the rate of progression of peripheral joint damage as measured by X-ray in patients with polyarticular symmetrical subtypes of the disease. Axial spondyloarthritis Ankylosing spondylitis Treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. Non-radiographic axial spondyloarthritis Treatment of adults with severe non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated C-reactive protein (CRP) and/or magnetic resonance imaging (MRI) evidence, who have had an inadequate response to nonsteroidal anti-inflammatory drugs (NSAIDs). Plaque psoriasis Treatment of adults with moderate to severe plaque psoriasis who failed to respond to, or who have a contraindication to, or are intolerant to other systemic therapy, including ciclosporin, methotrexate or psoralen and ultraviolet-A light (PUVA). Paediatric plaque psoriasis Treatment of chronic severe plaque psoriasis in children and adolescents from the age of 6 years who are inadequately controlled by, or are intolerant to, other systemic therapies or phototherapies.

От официалната листовка · 2026-09-30 · European Medicines Agency

Същото активно вещество, концентрация и форма в други държави

Съпоставени само по активно вещество, концентрация и вид лекарствена форма. Това не означава, че продуктите са еквивалентни или взаимозаменяеми: помощните вещества, освобождаването и одобрените показания може да се различават — попитайте фармацевт преди замяна.

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САЩНяма точно съвпадение за тази концентрация и форма

ИспанияНяма точно съвпадение за тази концентрация и форма

КанадаНяма точно съвпадение за тази концентрация и форма

НидерландияНяма точно съвпадение за тази концентрация и форма

ШвейцарияНяма точно съвпадение за тази концентрация и форма

Подробности

ПроизводителBiosimilar Collaborations Ireland Limited
Активно веществоEtanercept
ГрупаОнкологични и имуномодулиращи лекарства
КласификацияL04AB01 · Онкологични и имуномодулиращи лекарства
БиоподобноДа — биоподобно лекарство, според регистъра
Разрешен на2020-05-20
Последна актуализация от регулатора2025-03-03
EMA product numberEMEA/H/C/004711

Източник: European Medicines Agency — medicine data · 2026-09-30 · не е прегледано от лекар

Source: European Medicines Agency (EMA). Product information as published by EMA. Условия за повторно използване: EMA legal notice (reproduction authorised).

Същото активно вещество

Съдържат същото вещество. Това не значи, че едното замества другото — попитайте фармацевт.