יומירה 40 מ"ג

País: Israel

Idioma: hebreo

Fuente: Ministry of Health

Ingredientes activos:

ADALIMUMAB 40 MG / 0.8 ML

Disponible desde:

ABBVIE BIOPHARMACEUTICALS LTD, ISRAEL

Código ATC:

L04AA17

formulario farmacéutico:

SOLUTION FOR INJECTION

Composición:

PEN

Vía de administración:

S.C

Fabricado por:

ABBVIE LTD, UK

Grupo terapéutico:

ADALIMUMAB

indicaciones terapéuticas:

* Rheumatoid arthritis: Humira in combination with methotrexate is indicated for: - the treatment of moderate to severe active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drugs including methotrexate has been inadequate. - the treatment of severe active and progressive rheumatoid arthritis in adults not previously treated with methotrexate. Humira can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate. Humira has been shown to reduce the rate of progression of joint damage as measured by X-ray adn to impove physical function when given in combination with methotrexate. * Crohn's disease : Humira is indicated for reducing signs and symptoms and inducing and maintaining clinical remission in adult patients with moderately to severely active Crohn's disease who have had an inadequate response to conventional therapy.Humira is indicated for reducing signs and symptoms and inducing clinical r

Fecha de autorización:

2009-07-01