Den Europæiske Union - dansk - EMA (European Medicines Agency)

n.v. organon - desloratadin - rhinitis, allergic, perennial; urticaria; rhinitis, allergic, seasonal - antihistaminer til systemisk brug, - azomyr is indicated for the relief of symptoms associated with:allergic rhinitis (see section 5. 1)urticaria (see section 5.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

pfizer europe ma eeig - vareniclin - anvendelse af tobaksbrug - andre narkotika stoffer - champix er indiceret til rygestop hos voksne.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

recordati rare diseases - mercaptaminbitartrat - cystinosis - andre alimentary tract and metabolism produkter, - cystagon er indiceret til behandling af bevist nefropatisk cystinose. cysteamin reducerer cystinakkumulering i nogle celler (f.eks. leukocytter, muskel- og leverceller) hos nephropatiske cystinose patienter, og når behandlingen påbegyndes tidligt forsinker det udviklingen af ​​nyresvigt.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

alexion europe sas - sebelipase alfa - lipid metabolisme, inborn fejl - andre alimentary tract and metabolism produkter, - kanuma er indiceret til langsigtet enzymbytningsbehandling (ert) hos patienter i alle aldre med lysosomalsyre lipase (lal) mangel.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

n.v. organon - desloratadin - rhinitis, allergic, perennial; urticaria; rhinitis, allergic, seasonal - antihistaminer til systemisk brug, - neoclarityn er indiceret til lindring af symptomer forbundet med allergisk rhinitisurticaria.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

santen oy - ciclosporin - conjunctivitis; keratitis - oftalmologiske - behandling af svær vernal keratoconjunctivitis (vkc) hos børn fra 4 år og unge.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

otsuka novel products gmbh - delamanid - tuberkulose, multidrugt-resistent - antimyco-bakterielle midler - deltyba is indicated for use as part of an appropriate combination regimen for pulmonary multi-drug resistant tuberculosis (mdr-tb) in adults, adolescents, children and infants with a body weight of at least 10 kg when an effective treatment regimen cannot otherwise be composed for reasons of resistance or tolerability (see sections 4. 2, 4. 4 og 5. det bør overvejes at officielle vejledning om hensigtsmæssig brug af antibakterielle midler..

Den Europæiske Union - dansk - EMA (European Medicines Agency)

glaxosmithkline dungarvan limited - esomeprazol - gastroøsofageal tilbagesvaling - proton pumpe hæmmere - nexium control er indiceret til kortvarig behandling af reflukssymptomer (f.eks. halsbrand og syreregurgitation) hos voksne.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

sandoz pharmaceuticals d.d. - zoledronsyre - osteoporosis; osteitis deformans; osteoporosis, postmenopausal - narkotika til behandling af knoglesygdomme - treatment of osteoporosis: , in post-menopausal women;, in men; , at increased risk of fracture, including those with a recent low-trauma hip fracture. behandling af osteoporose, der er forbundet med langtids systemisk glukokortikoid behandling i post-menopausale kvinder og mænd med øget risiko for fraktur. behandling af pagets sygdom af knoglerne.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

vertex pharmaceuticals (ireland) limited - ivacaftor - cystisk fibrose - andet respirationssystem produkter - 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.