Copalia Evrópusambandið - íslenska - EMA (European Medicines Agency)

copalia

novartis europharm limited - valsartan, amlodipine (as amlodipine besilate) - háþrýstingur - lyf sem hafa áhrif á renín-angíótensín kerfið - meðferð við nauðsynlegum háþrýstingi. copalia er ætlað sjúklingum sem blóðþrýstingur er ekki nægilega stjórn á meðferð eða valsartan sér.

Exforge Evrópusambandið - íslenska - EMA (European Medicines Agency)

exforge

novartis europharm limited - valsartan, amlodipine (as amlodipine besilate) - háþrýstingur - lyf sem hafa áhrif á renín-angíótensín kerfið - meðferð við nauðsynlegum háþrýstingi. exforge er ætlað sjúklingum sem blóðþrýstingur er ekki nægilega stjórn á meðferð eða valsartan sér.

Rivaroxaban Viatris (previously Rivaroxaban Mylan) Evrópusambandið - íslenska - EMA (European Medicines Agency)

rivaroxaban viatris (previously rivaroxaban mylan)

mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - blóðþurrðandi lyf - 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.

Sitagliptin/Metformin Medical Valley Filmuhúðuð tafla 50mg/1000 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sitagliptin/metformin medical valley filmuhúðuð tafla 50mg/1000 mg

medical valley invest ab - metforminum hýdróklóríð; sitagliptinum hýdróklóríð - filmuhúðuð tafla - 50mg/1000 mg

Sitagliptin/Metformin Medical Valley Filmuhúðuð tafla 50mg/850 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sitagliptin/metformin medical valley filmuhúðuð tafla 50mg/850 mg

medical valley invest ab - sitagliptinum hýdróklóríð; metforminum hýdróklóríð - filmuhúðuð tafla - 50mg/850 mg

Terbinafin Medical Valley Tafla 250 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

terbinafin medical valley tafla 250 mg

medical valley invest ab - terbinafinum hýdróklóríð - tafla - 250 mg

Valganciclovir Medical Valley Filmuhúðuð tafla 450 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

valganciclovir medical valley filmuhúðuð tafla 450 mg

medical valley invest ab - valganciclovirum hýdróklóríð - filmuhúðuð tafla - 450 mg