Klacid OD 500 mg Norge - norsk - Statens legemiddelverk

klacid od 500 mg

viatris as - klaritromycin - depottablett - 500 mg

Ery-Max 250 mg Norge - norsk - Statens legemiddelverk

ery-max 250 mg

meda - asker - erytromycin - enterokapsel, hard - 250 mg

Klacid OD 500 mg Norge - norsk - Statens legemiddelverk

klacid od 500 mg

orifarm as - klaritromycin - depottablett - 500 mg

Kalydeco Den europeiske union - norsk - EMA (European Medicines Agency)

kalydeco

vertex pharmaceuticals (ireland) limited - ivacaftor - cystisk fibrose - andre åndedrettsprodukter - 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 og 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 og 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.

Rosuvastatin Xiromed 20 mg Norge - norsk - Statens legemiddelverk

rosuvastatin xiromed 20 mg

medical valley invest ab - rosuvastatinkalsium - tablett, filmdrasjert - 20 mg

Rosuvastatin Xiromed 5 mg Norge - norsk - Statens legemiddelverk

rosuvastatin xiromed 5 mg

medical valley invest ab - rosuvastatinkalsium - tablett, filmdrasjert - 5 mg

Rosuvastatin Xiromed 10 mg Norge - norsk - Statens legemiddelverk

rosuvastatin xiromed 10 mg

medical valley invest ab - rosuvastatinkalsium - tablett, filmdrasjert - 10 mg

Rosuvastatin Xiromed 40 mg Norge - norsk - Statens legemiddelverk

rosuvastatin xiromed 40 mg

medical valley invest ab - rosuvastatinkalsium - tablett, filmdrasjert - 40 mg

Symkevi Den europeiske union - norsk - EMA (European Medicines Agency)

symkevi

vertex pharmaceuticals (ireland) limited - tezacaftor, ivacaftor - cystisk fibrose - andre åndedrettsprodukter - 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.

Desirett 75 mikrog Norge - norsk - Statens legemiddelverk

desirett 75 mikrog

exeltis healthcare s.l. (1) - desogestrel - tablett, filmdrasjert - 75 mikrog