Ευρωπαϊκή Ένωση - Νορβηγικά - EMA (European Medicines Agency)

accord healthcare s.l.u. - rivaroksaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - antithrombotic agents - forebygging av venøs tromboembolisme (vte) hos voksne pasienter som gjennomgår valgfri hofte- eller kneutskifting. behandling av dyp venetrombose (dvt) og lungeemboli (pe), og forebygging av tilbakevendende dvt og pe i voksne. (see section 4. 4 for haemodynamically unstable pe patients. behandling av dyp venetrombose (dvt) og lungeemboli (pe), og forebygging av tilbakevendende dvt og pe i voksne. (see section 4. 4 for haemodynamically ustabil pe pasienter). adultsprevention of stroke and systemic embolism in adult patients with non valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. behandling av dyp venetrombose (dvt) og lungeemboli (pe), og forebygging av tilbakevendende dvt og pe i voksne. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. rivaroxaban accord, co administered with acetylsalicylic acid (asa) alone or with asa plus ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers (see sections 4. 3, 4. 4 og 5. rivaroxaban accord, co administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. behandling av dyp venetrombose (dvt) og lungeemboli (pe), og forebygging av tilbakevendende dvt og pe i voksne. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Ευρωπαϊκή Ένωση - Νορβηγικά - EMA (European Medicines Agency)

mylan s.a.s. - docetaxel - head and neck neoplasms; carcinoma, non-small-cell lung; adenocarcinoma; prostatic neoplasms; breast neoplasms - antineoplastiske midler - behandling av brystkreft, spesielle former for lungekreft (ikke-småcellet lungekreft), prostatakreft, magekreft eller hode og hals kreft.

Ευρωπαϊκή Ένωση - Νορβηγικά - EMA (European Medicines Agency)

cheplapharm arzneimittel gmbh - verteporfin - myopia, degenerative; macular degeneration - Øyemidler - visudyne er angitt for behandling av:voksne med exudative (våt) aldersrelatert makuladegenerasjon (amd) med overveiende klassisk subfoveal choroidal neovascularisation (cnv) eller;voksne med subfoveal choroidal neovascularisation sekundær til patologisk myopi.

Νορβηγία - Νορβηγικά - Statens legemiddelverk

ge healthcare ltd - krom (51cr) edetat - injeksjonsvæske, oppløsning - 3.7 mbq/ ml

Νορβηγία - Νορβηγικά - Statens legemiddelverk

cis bio international - natriumjodid (131 i) - kapsel, hard - 50 mbq

Νορβηγία - Νορβηγικά - Statens legemiddelverk

curium netherlands b.v. - jobenguansulfat (123i) - injeksjonsvæske, oppløsning - 74 mbq/ ml

Νορβηγία - Νορβηγικά - Statens legemiddelverk

curium netherlands b.v. - indium (111in) klorid / pentetreotid - preparasjonssett til radioaktive legemidler - 111 mbq/ ml / 10 mikrog

Νορβηγία - Νορβηγικά - Statens legemiddelverk

ge healthcare b.v. - natriumjodid (123i) - injeksjonsvæske, oppløsning - 37 mbq/ ml

Νορβηγία - Νορβηγικά - Statens legemiddelverk

curium netherlands b.v. - natriumjodid (131i) - kapsel, hard

Νορβηγία - Νορβηγικά - Statens legemiddelverk

ge healthcare b.v. - fludeoksyglukose (18f) - injeksjonsvæske, oppløsning - 250 mbq/ ml