Anagrelide ratiopharm 0.5 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

anagrelide ratiopharm 0.5 mg kapseli, kova

teva b.v. - anagrelide hydrochloride monohydrate - kapseli, kova - 0.5 mg - anagrelidi

Anagrelide Sandoz 0.5 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

anagrelide sandoz 0.5 mg kapseli, kova

sandoz a/s - anagrelide hydrochloride monohydrate - kapseli, kova - 0.5 mg - anagrelidi

Anagrelide Stada 0.5 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

anagrelide stada 0.5 mg kapseli, kova

stada arzneimittel ag - anagrelide hydrochloride monohydrate - kapseli, kova - 0.5 mg - anagrelidi

Imatinib Koanaa Euroopan unioni - suomi - EMA (European Medicines Agency)

imatinib koanaa

koanaa healthcare gmbh - imatinib mesilate - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - antineoplastiset aineet - imatinib koanaa is indicated for the treatment ofadult and paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment. adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. adult and paediatric patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy. adult patients with relapsed or refractory ph+ all as monotherapy. adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements. adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfrα rearrangement. the effect of imatinib on the outcome of bone marrow transplantation has not been determined. imatinib koanaa is indicated forthe treatment of adult patients with kit (cd 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (gist). the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. potilaat, joilla on alhainen tai hyvin alhainen riski toistumisen pitäisi saada adjuvanttihoitona. the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic gist and dfsp and on recurrence-free survival in adjuvant gist. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. paitsi äskettäin diagnosoitu kroonisen vaiheen kml, ei ole kontrolloituja tutkimuksia, jotka osoittaisivat kliinistä tehoa tai eloonjäämisetua näissä sairauksia.

CAPECITABINE KOANAA 150 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

capecitabine koanaa 150 mg tabletti, kalvopäällysteinen

koanaa healthcare gmbh - capecitabinum - tabletti, kalvopäällysteinen - 150 mg - kapesitabiini

CAPECITABINE KOANAA 500 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

capecitabine koanaa 500 mg tabletti, kalvopäällysteinen

koanaa healthcare gmbh - capecitabinum - tabletti, kalvopäällysteinen - 500 mg - kapesitabiini

Anagrelide Mylan Euroopan unioni - suomi - EMA (European Medicines Agency)

anagrelide mylan

mylan pharmaceuticals limited - anagrelidi hydrochloride - trombosytemia, essential - antineoplastiset aineet - anagrelidi on tarkoitettu vähentämään kohonnut verihiutaleiden määrän vaarassa essentiaalista trombosytemiaa (et) potilailla, jotka eivät siedä heidän nykyistä hoitoa tai joiden kohonnut trombosyyttiarvo ole vähennetty hyväksyttävälle tasolle niiden nykyinen hoito. an at-risk patientan at-risk essential thrombocythaemia patient is defined by one or more of the following features:>60 years of age ora platelet count >1,000 x 10⁹/l ora history of thrombo-haemorrhagic events.

IMATINIB KOANAA 100 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

imatinib koanaa 100 mg tabletti, kalvopäällysteinen

koanaa healthcare gmbh - imatinibi mesylas - tabletti, kalvopäällysteinen - 100 mg - imatinibi

IMATINIB KOANAA 400 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

imatinib koanaa 400 mg tabletti, kalvopäällysteinen

koanaa healthcare gmbh - imatinibi mesylas - tabletti, kalvopäällysteinen - 400 mg - imatinibi

CLOFARABINE KOANAA 1 mg/ml infuusiokonsentraatti, liuosta varten Suomi - suomi - Fimea (Suomen lääkevirasto)

clofarabine koanaa 1 mg/ml infuusiokonsentraatti, liuosta varten

koanaa healthcare gmbh - clofarabinum - infuusiokonsentraatti, liuosta varten - 1 mg/ml - klofarabiini