zyclara
viatris healthcare limited - imiquimod - keratosis; keratosis, actinic - sýklalyf og krabbameinslyf til dýrafræðilegrar notkunar - zyclara er ætlað fyrir baugi meðferð vísindalega dæmigert, ekki hyperkeratotic, ekki læknafélag, sýnileg eða teljandi geislunarhyrning fullt andlit eða sköllóttur höfði í ónæmiskerfi fullorðnir þegar öðrum baugi meðferð möguleikar eru handa eða minna viðeigandi.
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
treo citrus freyðitafla 500/50 mg
viatris aps - acidum acetylsalicylicum; coffeinum - freyðitafla - 500/50 mg
creon (pankreon) magasýruþolið hart hylki 10.000
viatris aps - pancreatinum - magasýruþolið hart hylki - 10.000
furadantin tafla 50 mg
viatris aps - nitrofurantoinum inn - tafla - 50 mg
furadantin tafla 5 mg
viatris aps - nitrofurantoinum inn - tafla - 5 mg
dymista nefúði, dreifa 137 míkróg / 50 míkróg/skammt
viatris aps - azelastinum hýdróklóríð; fluticasonum própíónat - nefúði, dreifa - 137 míkróg / 50 míkróg/skammt
amoxicillin mylan (amoxicillin mylan) tafla 750 mg
viatris limited - amoxicillinum tríhýdrat - tafla - 750 mg
amoxicillin mylan (amoxicillin mylan) hart hylki 500 mg
viatris limited - amoxicillinum tríhýdrat - hart hylki - 500 mg