quetiapine alvogen (quetiapine teva) filmuhúðuð tafla 100 mg
alvogen ehf. - quetiapinum fúmarat - filmuhúðuð tafla - 100 mg
quetiapine alvogen (quetiapin ratiopharm) forðatafla 50 mg
alvogen ehf. - quetiapinum fúmarat - forðatafla - 50 mg
quetiapine alvogen (quetiapine teva) filmuhúðuð tafla 200 mg
alvogen ehf. - quetiapinum fúmarat - filmuhúðuð tafla - 200 mg
quetiapine alvogen (quetiapine teva) filmuhúðuð tafla 25 mg
alvogen ehf. - quetiapinum fúmarat - filmuhúðuð tafla - 25 mg
quetiapine alvogen (quetiapin ratiopharm) forðatafla 200 mg
alvogen ehf. - quetiapinum fúmarat - forðatafla - 200 mg
quetiapine alvogen (quetiapin ratiopharm) forðatafla 300 mg
alvogen ehf. - quetiapinum fúmarat - forðatafla - 300 mg
quetiapine alvogen (quetiapin ratiopharm) forðatafla 400 mg
alvogen ehf. - quetiapinum fúmarat - forðatafla - 400 mg
dasatinib accord
accord healthcare s.l.u. - dasatinib - precursor cell lymphoblastic leukemia-lymphoma; leukemia, myelogenous, chronic, bcr-abl positive - Æxlishemjandi lyf - dasatinib accord is indicated for the treatment of adult patients with:• ph+ acute lymphoblastic leukaemia (all) with resistance or intolerance to prior therapy. dasatinib accord is indicated for the treatment of paediatric patients with:• newly diagnosed ph+ all in combination with chemotherapy.
dasatinib accordpharma
accord healthcare s.l.u. - dasatinib - precursor cell lymphoblastic leukemia-lymphoma; leukemia, myelogenous, chronic, bcr-abl positive - Æxlishemjandi lyf - dasatinib accordpharma is indicated for the treatment of adult patients with: newly diagnosed philadelphia chromosome positive (ph+) chronic myelogenous leukaemia (cml) in the chronic phase. chronic, accelerated or blast phase cml with resistance or intolerance to prior therapy including imatinib. ph+ acute lymphoblastic leukaemia (all) and lymphoid blast cml with resistance or intolerance to prior therapy. dasatinib accordpharma is indicated for the treatment of paediatric patients with: newly diagnosed ph+ cml in chronic phase (ph+ cml-cp) or ph+ cml-cp resistant or intolerant to prior therapy including imatinib. newly diagnosed ph+ all in combination with chemotherapy.
leflunomide teva
teva pharma b.v. - leflúnómíð - liðagigt, liðagigt - Ónæmisbælandi lyf - leflúnómíð er ætlað til meðferðar hjá fullorðnum sjúklingum með virkan iktsýki sem "sjúkdómsbreytileg andnæmislyf" (dmard). undanförnum eða samhliða meðferð með lifur eða haematotoxic sjúkdómstemprandi (e. stendur) getur leitt til aukinnar hættu alvarleg neikvæð viðbrögð; því upphaf leflúnómíð meðferð hefur verið vandlega um þetta gagnast / hættu þætti. Þar að auki, skipta úr leflúnómíð til annars dmard án eftir washout aðferð geta líka aukið hættuna af alvarlegum neikvæð viðbrögð jafnvel í langan tíma eftir að skipta.