יומירה 40 מ"ג

Ülke: İsrail

Dil: İbranice

Kaynak: Ministry of Health

Aktif bileşen:

ADALIMUMAB 40 MG / 0.8 ML

Mevcut itibaren:

ABBVIE BIOPHARMACEUTICALS LTD, ISRAEL

ATC kodu:

L04AA17

Farmasötik formu:

SOLUTION FOR INJECTION

Kompozisyon:

PEN

Uygulama yolu:

S.C

Tarafından üretildi:

ABBVIE LTD, UK

Terapötik grubu:

ADALIMUMAB

Terapötik endikasyonlar:

* 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

Yetkilendirme tarihi:

2009-07-01