caredin 2.5 mg tabletti, suussa hajoava
2care4 generics aps - desloratadine - tabletti, suussa hajoava - 2.5 mg - desloratadiini
caredin 5 mg tabletti, suussa hajoava
2care4 generics aps - desloratadine - tabletti, suussa hajoava - 5 mg - desloratadiini
flurhin 50 mikrog/annos nenäsumute, suspensio
2care4 generics aps - fluticasone propionate - nenäsumute, suspensio - 50 mikrog/annos - flutikasoni
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.
prosterid 1 mg tabletti, kalvopäällysteinen
2care4 generics aps - finasteride - tabletti, kalvopäällysteinen - 1 mg - finasteridi
kaliumklorid orifarm 1 g depottabletti
orifarm generics a/s - potassium chloride - depottabletti - 1 g - kaliumkloridi
clotaxip 150 mikrog/ml injektioneste, liuos
2care4 generics aps - clonidine hydrochloride - injektioneste, liuos - 150 mikrog/ml - klonidiini
rilonacept regeneron (previously arcalyst)
regeneron uk limited - rilonacept - cryopyrin liittyvien oireyhtymien - immunosuppressantit - rilonacept regeneron ilmoitetaan cryopyrin liittyvä kausittainen oireyhtymät (caps) hoitoon vakavia oireita, kuten familiaalinen kylmä auto tulehduksellinen oireyhtymä (fcas) ja muckle wells oireyhtymä (mws) aikuisilla ja 12 vuotiaat lapset ja vanhemmat.
ramipril medgenerics 1.25 mg tabletti
sanofi-aventis oy - ramiprilum - tabletti - 1.25 mg - ramipriili
ramipril medgenerics 2.5 mg tabletti
sanofi-aventis oy - ramiprilum - tabletti - 2.5 mg - ramipriili