Apixaban Accord Den europeiske union - norsk - EMA (European Medicines Agency)

apixaban accord

accord healthcare s.l.u. - apixaban - venous thromboembolism; stroke; arthroplasty - antithrombotic agents - prevention of venous thromboembolic events (vte) in adult patients who have undergone elective hip or knee replacement surgery. forebygging av slag og systemisk emboli hos voksne pasienter med ikke-valvulær atrieflimmer (nvaf), med én eller flere risikofaktorer, slik som tidligere hjerneslag eller forbigående ischaemic angrep (tia); alder ≥ 75 år, hypertensjon; diabetes mellitus; symptomatisk hjertesvikt (nyha klasse ≥ ii). behandling av dyp venetrombose (dvt) og lungeemboli (pe), og forebygging av tilbakevendende dvt og pe i voksne (se kapittel 4. 4 for haemodynamically ustabil pe pasienter). prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation (nvaf), with one or more risk factors, such as prior stroke or transient ischaemic attack (tia); age≥ 75 years; hypertension; diabetes mellitus; symptomatic heart failure (nyha class ≥ ii). behandling av dyp venetrombose (dvt) og lungeemboli (pe), og forebygging av tilbakevendende dvt og pe i voksne (se kapittel 4. 4 for haemodynamically ustabil pe pasienter).

Rivaroxaban Viatris (previously Rivaroxaban Mylan) Den europeiske union - norsk - EMA (European Medicines Agency)

rivaroxaban viatris (previously rivaroxaban mylan)

mylan ireland limited - rivaroksaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - antithrombotic agents - rivaroxaban mylan co-administered with acetylsalicylic acid (asa) alone or with asa plus clopidogrel or ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers.  rivaroxaban mylan 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.  ------prevention of venous thromboembolism (vte) in adult patients undergoing elective hip or knee replacement surgery.  treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and prevention of recurrent dvt and pe in adults. -------adults prevention 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. paediatric population treatment 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. paediatric population treatment 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.

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

entyvio

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - selektive immunosuppressiva - ulcerøs colitisentyvio er indisert for behandling av voksne pasienter med moderat til alvorlig aktiv ulcerøs kolitt som har hatt utilstrekkelig respons med, mistet svar på, eller var intolerant å enten konvensjonell terapi eller en tumor nekrose faktor alfa (tnfa) antagonist. crohns diseaseentyvio er indisert for behandling av voksne pasienter med moderat til alvorlig aktiv crohns sykdom som har hatt utilstrekkelig respons med, mistet svar på, eller var intolerant å enten konvensjonell terapi eller en tumor nekrose faktor alfa (tnfa) antagonist. pouchitisentyvio is indicated for the treatment of adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for ulcerative colitis, and have had an inadequate response with or lost response to antibiotic therapy.

Valsartan/Hydrochlorothiazide Sandoz 80 mg / 12.5 mg Norge - norsk - Statens legemiddelverk

valsartan/hydrochlorothiazide sandoz 80 mg / 12.5 mg

sandoz - københavn - valsartan / hydroklortiazid - tablett, filmdrasjert - 80 mg / 12.5 mg

Valsartan/Hydrochlorothiazide Sandoz 160 mg / 12.5 mg Norge - norsk - Statens legemiddelverk

valsartan/hydrochlorothiazide sandoz 160 mg / 12.5 mg

sandoz - københavn - valsartan / hydroklortiazid - tablett, filmdrasjert - 160 mg / 12.5 mg

Valsartan/Hydrochlorothiazide Sandoz 160 mg / 25 mg Norge - norsk - Statens legemiddelverk

valsartan/hydrochlorothiazide sandoz 160 mg / 25 mg

sandoz - københavn - valsartan / hydroklortiazid - tablett, filmdrasjert - 160 mg / 25 mg

Paroxetin Hexal 20 mg Norge - norsk - Statens legemiddelverk

paroxetin hexal 20 mg

hexal a/s - paroksetinhydroklorid - tablett, filmdrasjert - 20 mg

Venlafaxin ratiopharm 37.5 mg Norge - norsk - Statens legemiddelverk

venlafaxin ratiopharm 37.5 mg

ratiopharm gmbh - venlafaksinhydroklorid - depotkapsel, hard - 37.5 mg

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

xadago

zambon spa - safinamidmetansulfonat - parkinsonsykdom - anti-parkinson medisiner - xadago er indisert for behandling av voksne pasienter med idiopatisk parkinsons sykdom (pd) som add-on terapi til en stabil dose levodopa (l-dopa) alene eller i kombinasjon med andre pd legemidler i midt-sent varierende pasienter.

Genvoya Norge - norsk - Statens legemiddelverk

genvoya

orifarm as - elvitegravir / kobicistat / emtricitabin / tenofoviralafenamidfumarat - tablett, filmdrasjert - 150 mg / 150 mg / 200 mg / 10 mg