Stilnoct Filmuhúðuð tafla 10 mg Islândia - islandês - LYFJASTOFNUN (Icelandic Medicines Agency)

stilnoct filmuhúðuð tafla 10 mg

sanofi-aventis norge as - zolpidemum tartrat - filmuhúðuð tafla - 10 mg

Flagyl Filmuhúðuð tafla 400 mg Islândia - islandês - LYFJASTOFNUN (Icelandic Medicines Agency)

flagyl filmuhúðuð tafla 400 mg

sanofi-aventis norge as - metronidazolum inn - filmuhúðuð tafla - 400 mg

Flagyl Leggangastíll 500 mg Islândia - islandês - LYFJASTOFNUN (Icelandic Medicines Agency)

flagyl leggangastíll 500 mg

sanofi-aventis norge as - metronidazolum inn - leggangastíll - 500 mg

Imovane Filmuhúðuð tafla 7,5 mg Islândia - islandês - LYFJASTOFNUN (Icelandic Medicines Agency)

imovane filmuhúðuð tafla 7,5 mg

sanofi-aventis norge as - zopiclonum inn - filmuhúðuð tafla - 7,5 mg

Orudis Hart forðahylki 100 mg Islândia - islandês - LYFJASTOFNUN (Icelandic Medicines Agency)

orudis hart forðahylki 100 mg

sanofi-aventis norge as - ketoprofenum inn - hart forðahylki - 100 mg

Solian Tafla 200 mg Islândia - islandês - LYFJASTOFNUN (Icelandic Medicines Agency)

solian tafla 200 mg

sanofi-aventis norge as - amisulpridum inn - tafla - 200 mg

Solian Tafla 50 mg Islândia - islandês - LYFJASTOFNUN (Icelandic Medicines Agency)

solian tafla 50 mg

sanofi-aventis norge as - amisulpridum inn - tafla - 50 mg

Iasibon União Europeia - islandês - EMA (European Medicines Agency)

iasibon

pharmathen s.a. - ibandrónsýra - hypercalcemia; fractures, bone; neoplasm metastasis; breast neoplasms - lyf til að meðhöndla beinsjúkdóma - concentrate for solution for infusion prevention of skeletal events (pathological fractures, bone complications requiring radiotherapy or surgery) in patients with breast cancer and bone metastases. meðferð æxli völdum álíka með eða án meinvörp. film-coated tablets prevention of skeletal events (pathological fractures, bone complications requiring radiotherapy or surgery) in patients with breast cancer and bone metastases.

Maviret União Europeia - islandês - EMA (European Medicines Agency)

maviret

abbvie deutschland gmbh co. kg - glecaprevir, pibrentasvir - lifrarbólga c, langvinn - veirueyðandi lyf til almennrar notkunar - maviret is indicated for the treatment of chronic hepatitis c virus (hcv) infection in adults and children aged 3 years and older. maviret coated granules is indicated for the treatment of chronic hepatitis c virus (hcv) infection in children 3 years and older.

Kalydeco União Europeia - islandês - EMA (European Medicines Agency)

kalydeco

vertex pharmaceuticals (ireland) limited - ivacaftor - cystic fibrosis - Önnur öndunarfæri - 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.