Atenolol Viatris 50 mg Norge - norsk - Statens legemiddelverk

atenolol viatris 50 mg

viatris limited - atenolol - tablett, filmdrasjert - 50 mg

Atenolol Viatris 25 mg Norge - norsk - Statens legemiddelverk

atenolol viatris 25 mg

viatris limited - atenolol - tablett, filmdrasjert - 25 mg

Atenolol Viatris 100 mg Norge - norsk - Statens legemiddelverk

atenolol viatris 100 mg

viatris limited - atenolol - tablett, filmdrasjert - 100 mg

Piroxicam Viatris 20 mg Norge - norsk - Statens legemiddelverk

piroxicam viatris 20 mg

viatris limited - piroksikam - tablett - 20 mg

Tamoxifen Viatris 20 mg Norge - norsk - Statens legemiddelverk

tamoxifen viatris 20 mg

viatris limited - tamoksifensitrat - tablett - 20 mg

Solifenacin Viatris 5 mg Norge - norsk - Statens legemiddelverk

solifenacin viatris 5 mg

viatris limited - solifenacinsuksinat - tablett, filmdrasjert - 5 mg

Solifenacin Viatris 10 mg Norge - norsk - Statens legemiddelverk

solifenacin viatris 10 mg

viatris limited - solifenacinsuksinat - tablett, filmdrasjert - 10 mg

Bortezomib Viatris 3.5 mg Norge - norsk - Statens legemiddelverk

bortezomib viatris 3.5 mg

viatris limited - bortezomibmannitolboronat - pulver til injeksjonsvæske, oppløsning - 3.5 mg

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.

Creon 35000 Norge - norsk - Statens legemiddelverk

creon 35000

viatris healthcare ltd. - lipase / amylase / protease - enterokapsel, hard - 35000 ie / 25200 ie / 1400 ie