Lextemy Európai Unió - izlandi - EMA (European Medicines Agency)

lextemy

mylan ire healthcare limited - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - Æxlishemjandi lyf - treatment of carcinoma of the colon or rectum, breast cancer, non-small cell lung cancer, renal cell cancer, epithelial ovarian, fallopian tube or primary peritoneal cancer, and carcinoma of the cervix.

Sorafenib Accord Európai Unió - izlandi - EMA (European Medicines Agency)

sorafenib accord

accord healthcare s.l.u. - sorafenib tosilate - carcinoma, hepatocellular; carcinoma, renal cell - Æxlishemjandi lyf - hepatocellular carcinomasorafenib accord is indicated for the treatment of hepatocellular carcinoma (see section 5. renal cell carcinomasorafenib accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.

Teriflunomide Mylan Európai Unió - izlandi - EMA (European Medicines Agency)

teriflunomide mylan

mylan pharmaceuticals limited - teriflunomide - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Teriflunomide Accord Európai Unió - izlandi - EMA (European Medicines Agency)

teriflunomide accord

accord healthcare s.l.u. - teriflunomide - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi, sérhæfður ónæmisbælandi - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Sandimmun Innrennslisþykkni, lausn 50 mg/ml Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

sandimmun innrennslisþykkni, lausn 50 mg/ml

novartis healthcare a/s - ciclosporinum inn - innrennslisþykkni, lausn - 50 mg/ml

Ondansetron Fresenius Kabi Stungulyf, lausn 2 mg/ml Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

ondansetron fresenius kabi stungulyf, lausn 2 mg/ml

fresenius kabi ab - ondansetronum hýdróklóríð - stungulyf, lausn - 2 mg/ml

Bortezomib Actavis Stungulyfsstofn, lausn 3,5 mg Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

bortezomib actavis stungulyfsstofn, lausn 3,5 mg

actavis group ptc ehf. - bortezomibum inn - stungulyfsstofn, lausn - 3,5 mg