Orkambi Euroopan unioni - suomi - EMA (European Medicines Agency)

orkambi

vertex pharmaceuticals (ireland) limited - lumacaftor, ivacaftor - kystinen fibroosi - muut hengitysteiden tuotteet - orkambi-tabletit on tarkoitettu kystisen fibroosin (cf) potilailla, jotka ovat iältään 6 vuotta ja vanhemmat, jotka ovat homotsygoottisia f508del-mutaation cftr geeni. orkambi granules are indicated for the treatment of cystic fibrosis (cf) in children aged 1 year and older who are homozygous for the f508del mutation in the cftr gene.

Kaftrio Euroopan unioni - suomi - EMA (European Medicines Agency)

kaftrio

vertex pharmaceuticals (ireland) limited - ivacaftor, tezacaftor, elexacaftor - kystinen fibroosi - muut hengitysteiden tuotteet - 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.

Kalydeco Euroopan unioni - suomi - EMA (European Medicines Agency)

kalydeco

vertex pharmaceuticals (ireland) limited - ivacaftor - kystinen fibroosi - muut hengitysteiden tuotteet - kalydeco tablets are indicated:as monotherapy for the treatment of adults, adolescents, and children aged 6 years and older and weighing 25 kg or more with cystic fibrosis (cf) who have an r117h cftr mutation or one of the following gating (class iii) mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene: g551d, g1244e, g1349d, g178r, g551s, s1251n, s1255p, s549n or s549r (see sections 4. 4 ja 5. in a combination regimen with tezacaftor/ivacaftor tablets for the treatment of adults, adolescents, and children aged 6 years and older with cystic fibrosis (cf) who are homozygous for the f508del mutation or who are heterozygous for the f508del mutation and have one of the following mutations in the 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. in a combination regimen with ivacaftor/tezacaftor/elexacaftor tablets for the treatment of adults, adolescents, and children aged 6 years and older with cystic fibrosis (cf) who have at least one f508del mutation in the cftr gene (see section 5. kalydeco granules are indicated for the treatment of infants aged at least 4 months, toddlers and children weighing 5 kg to less than 25 kg with cystic fibrosis (cf) who have an r117h cftr mutation or one of the following gating (class iii) mutations in the cftr gene: g551d, g1244e, g1349d, g178r, g551s, s1251n, s1255p, s549n or s549r (see sections 4. 4 ja 5. in a combination regimen with ivacaftor/tezacaftor/elexacaftor for the treatment of cystic fibrosis (cf) in paediatric patients aged 2 to less than 6 years who have at least one f508del mutation in the cftr gene.

Symkevi Euroopan unioni - suomi - EMA (European Medicines Agency)

symkevi

vertex pharmaceuticals (ireland) limited - tezacaftor, ivacaftor - kystinen fibroosi - muut hengitysteiden tuotteet - 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.

Sporanox 100 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sporanox 100 mg kapseli, kova

janssen-cilag oy - itraconazole - kapseli, kova - 100 mg - itrakonatsoli

Sporanox 10 mg/ml oraaliliuos Suomi - suomi - Fimea (Suomen lääkevirasto)

sporanox 10 mg/ml oraaliliuos

janssen-cilag oy - itraconazole - oraaliliuos - 10 mg/ml - itrakonatsoli

Paxlovid Euroopan unioni - suomi - EMA (European Medicines Agency)

paxlovid

pfizer europe ma eeig - nirmatrelvir, ritonavir - covid-19 virus infection - paxlovid is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe covid 19.

Delstrigo Euroopan unioni - suomi - EMA (European Medicines Agency)

delstrigo

merck sharp & dohme b.v. - doravirine, lamivudiini, tenofoviiridisoproksiilifumaraatti - hiv-infektiot - antiviraalit hiv-infektioiden hoitoon, yhdistelmät - delstrigo on tarkoitettu hoitoon aikuisille hiv-1 ilman menneisyyden tai nykyisyyden todisteita resistenssi nnrti-luokan, lamivudiinia tai tenofoviirin. delstrigo is also indicated for the treatment of adolescents aged 12 years and older weighing at least 35 kg who are infected with hiv-1 without past or present evidence of resistance to the nnrti class, lamivudine, or tenofovir and who have experienced toxicities which preclude the use of other regimens that do not contain tenofovir disoproxil.

GHRYVELIN (previously Macimorelin Aeterna Zentaris) Euroopan unioni - suomi - EMA (European Medicines Agency)

ghryvelin (previously macimorelin aeterna zentaris)

atnahs pharma netherlands b.v. - macimorelin asetaatti - diagnostisia tekniikoita, hormonitoimintaa - macimorelin - tämä lääkevalmiste on tarkoitettu vain diagnostiseen käyttöön.  ghryvelin is indicated for the diagnosis of growth hormone deficiency (ghd) in adults.

Diflucan 150 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

diflucan 150 mg kapseli, kova

pfizer oy - fluconazole - kapseli, kova - 150 mg - flukonatsoli