GEMCITABINE ACTAVIS 200 MG/VIAL

Negara: Israel

Bahasa: Inggris

Sumber: Ministry of Health

Bahan aktif:

GEMCITABINE 200 MG/VIAL

Tersedia dari:

DEVRIES & CO. LTD

Kode ATC:

L01BC05

Bentuk farmasi:

POWDER FOR SOLUTION FOR INFUSION

Rute administrasi :

I.V

Diproduksi oleh:

ACTAVIS GROUP PTC ehf, ICELAND

Kelompok Terapi:

GEMCITABINE

Indikasi Terapi:

Gemcitabine is indicated for the treatment of locally advanced or metastatic bladder cancer in combination with cisplatin. Gemcitabine is indicated for treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas.Gemcitabine, in combination with cisplatin is indicated as first line treatment of patients with locally advanced or metastatic non-small cell lung cancer (NSCLC). Gemcitabine monotherapy can be considered in elderly patients or those with performance status 2. Gemcitabine is indicated for the treatment of patients with locally advanced or metastatic epithelial ovarian carcinoma, in combination with carboplatin, in patients with relapsed disease following a recurrence-free interval of at least 6 months after platinum-based, first-line therapy. Gemcitabine, in combination with paclitaxel, is indicated for the treatment of patients with unresectable, locally recurrent or metastatic breast cancer who have relapsed following adjuvant/neoadjuvant chemotherapy. Prior chemotherap

Tanggal Otorisasi:

2013-06-01