symkevi
vertex pharmaceuticals (ireland) limited - tezacaftor, ivacaftor - tsüstiline fibroos - muud hingamisteede tooted - symkevi is indicated in a combination regimen with ivacaftor tablets for the treatment of patients with cystic fibrosis (cf) aged 6 years and older who are homozygous for the f508del mutation or who are heterozygous for the f508del mutation and have one of the following mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene: p67l, r117c, l206w, r352q, a455e, d579g, 711+3a→g, s945l, s977f, r1070w, d1152h, 2789+5g→a, 3272 26a→g, and 3849+10kbc→t.
gemcitabine stada infusioonilahuse kontsentraat
stada arzneimittel ag - gemtsitabiin - infusioonilahuse kontsentraat - 38mg 1ml 39.5ml 1tk; 38mg 1ml 5.26ml 1tk; 38mg 1ml 52.6ml 1tk; 38mg 1ml 26.3ml 1tk
spiriva respimat inhalatsioonilahus
boehringer ingelheim international gmbh - tiotroopium - inhalatsioonilahus - 2,5mcg 1annus 60annus 2tk; 2,5mcg 1annus 60annus 1tk; 2,5mcg 1annus 60annus 3tk; 2,5mcg 1annus 60annus 8tk
riluzole stada 50mg õhukese polümeerikattega tablett
stada arzneimittel ag - rilusool - õhukese polümeerikattega tablett - 50mg 14tk; 50mg 112tk; 50mg 140tk; 50mg 98tk; 50mg 20tk; 50mg 168tk; 50mg 56tk; 50mg 84tk
pulmozyme nebuliseeritav lahus
roche eesti osaühing - alfadornaas - nebuliseeritav lahus - 1mg 1ml 2.5ml 6tk
riluzole esp pharma õhukese polümeerikattega tablett
esp pharma limited - rilusool - õhukese polümeerikattega tablett - 50mg 56tk
aerrane inhalatsiooniaur, lahus
baxter - isofluraan - inhalatsiooniaur, lahus - 250ml 1tk
travoprost/timolol stada silmatilgad, lahus
stada arzneimittel ag - timolool+travoprost - silmatilgad, lahus - 5mg+40mcg 1ml 2.5ml 3tk; 5mg+40mcg 1ml 2.5ml 6tk
kaftrio
vertex pharmaceuticals (ireland) limited - ivacaftor, tezacaftor, elexacaftor - tsüstiline fibroos - muud hingamisteede tooted - kaftrio is indicated in a combination regimen with ivacaftor for the treatment of cystic fibrosis (cf) in patients aged 6 years and older who have at least one f508del mutation in the cystic fibrosis transmembrane conductance regulator (cftr) gene.