naproxen viatris (naproxen mylan) tafla 500 mg
viatris limited - naproxenum inn - tafla - 500 mg
quetiapin viatris filmuhúðuð tafla 100 mg
viatris limited - quetiapinum fúmarat - filmuhúðuð tafla - 100 mg
quetiapin viatris filmuhúðuð tafla 25 mg
viatris limited - quetiapinum fúmarat - filmuhúðuð tafla - 25 mg
sotalol viatris (sotalol mylan) tafla 40 mg
viatris limited - sotalolum hýdróklóríð - tafla - 40 mg
sotalol viatris (sotalol mylan) tafla 80 mg
viatris limited - sotalolum hýdróklóríð - tafla - 80 mg
tamsulosin viatris (tamsulosin mylan 0,4 mg hart hylki með breyttan losunarhraða) hart hylki með breyttan losunarhraða 0,4 mg
viatris limited - tamsulosinum hýdróklóríð - hart hylki með breyttan losunarhraða - 0,4 mg
mysildecard
viatris limited - síldenafílsítrat - háþrýstingur, lungnabólga - Þvaglát - adultstreatment fullorðinna sjúklinga með lungum háþrýsting flokkast sem hagnýtur ii og iii, til að bæta æfing getu. verkun hefur verið sýnd í frumum lungnaháþrýstingi og lungnaháþrýstingi sem tengist bandvefssjúkdómum. börn populationtreatment af börnum sjúklinga á aldrinum 1 ár til 17 ára gamall með lungum háþrýsting. verkun með tilliti til endurbóta á æfingargetu eða lungnablóðþrýstingi hefur sést við frumháþrýstingi og lungnaháþrýstingi sem tengist meðfæddan hjartasjúkdóm (sjá kafla 5.
talmanco (previously tadalafil generics)
viatris limited - tadalafil - háþrýstingur, lungnabólga - Þvaglát - talmanco er ætlað í fullorðnir fyrir meðferð lungum slagæð háan blóðþrýsting (pah) flokkast sem hagnýtur ii og iii, til að bæta æfing getu. verkun hefur verið sýnd í sjálfvakta pah (ipah) og í pah í tengslum við krabbameinsvaldandi sjúkdóma.
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.
fem-mono retard forðatafla 60 mg
viatris limited - isosorbidi mononitras inn - forðatafla - 60 mg