Sodium Iodide [123I] Injection GE Healthcare 37 MBq/ ml Norwe - Kinorwe - Statens legemiddelverk

sodium iodide [123i] injection ge healthcare 37 mbq/ ml

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

Sodium Iodide [123I] Injection Curiumpharma 37 MBq/ ml Norwe - Kinorwe - Statens legemiddelverk

sodium iodide [123i] injection curiumpharma 37 mbq/ ml

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

Lescol Depot 80 mg Norwe - Kinorwe - Statens legemiddelverk

lescol depot 80 mg

orifarm as - fluvastatinnatrium - depottablett - 80 mg

Lescol Depot 80 mg Norwe - Kinorwe - Statens legemiddelverk

lescol depot 80 mg

orifarm as - fluvastatinnatrium - depottablett - 80 mg

Lescol Depot 80 mg Norwe - Kinorwe - Statens legemiddelverk

lescol depot 80 mg

orifarm as - fluvastatinnatrium - depottablett - 80 mg

Lescol Depot 80 mg Norwe - Kinorwe - Statens legemiddelverk

lescol depot 80 mg

orifarm as - fluvastatinnatrium - depottablett - 80 mg

Lumeblue (previously known as Methylthioninium chloride Cosmo) Umoja wa Ulaya - Kinorwe - EMA (European Medicines Agency)

lumeblue (previously known as methylthioninium chloride cosmo)

alfasigma s.p.a. - metyltioniniumklorid - colorectal neoplasms; colonoscopy - other diagnostic agents - lumeblue is indicated as a diagnostic agent enhancing visualisation of colorectal lesions in adult patients undergoing screening or surveillance colonoscopy.

Micardis 80 mg Norwe - Kinorwe - Statens legemiddelverk

micardis 80 mg

2care4 aps - telmisartan - tablett - 80 mg

Rivaroxaban Accord Umoja wa Ulaya - Kinorwe - EMA (European Medicines Agency)

rivaroxaban accord

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.