Azacitidine Mylan European Union - English - EMA (European Medicines Agency)

azacitidine mylan

mylan ireland limited - azacitidine - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastic agents - azacitidine mylan is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with:intermediate 2 and high risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29% marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30% blasts and multi lineage dysplasia, according to world health organisation (who) classification,aml with > 30% marrow blasts according to the who classification.

Arsenic trioxide Mylan European Union - English - EMA (European Medicines Agency)

arsenic trioxide mylan

mylan ireland limited - arsenic trioxide - leukemia, promyelocytic, acute - antineoplastic agents - arsenic trioxide mylan is indicated for induction of remission, and consolidation in adult patients with:- newly diagnosed low to intermediate risk acute promyelocytic leukaemia (apl) (white blood cell count, ≤ 10 x 103/μl) in combination with all trans retinoic acid (atra)- relapsed/refractory acute promyelocytic leukaemia (apl) (previous treatment should have included a retinoid and chemotherapy)characterised by the presence of the t(15;17) translocation and/or the presence of the promyelocytic leukaemia/retinoic acid receptor alpha (pml/rar alpha) gene.the response rate of other acute myelogenous leukaemia subtypes to arsenic trioxide has not beenexamined.

Rivaroxaban Viatris (previously Rivaroxaban Mylan) European Union - English - 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 - 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. 

Lamivudine/Zidovudine Mylan 150mg/300mg Film-coated tablet Malta - English - Medicines Authority

lamivudine/zidovudine mylan 150mg/300mg film-coated tablet

mylan pharmaceuticals limited damastown industrial park mulhuddart dublin15 dublin, ireland - zidovudine, lamivudine - film-coated tablet - zidovudine 300 mg lamivudine 150 mg - antivirals for systemic use

Dimethyl fumarate Mylan European Union - English - EMA (European Medicines Agency)

dimethyl fumarate mylan

mylan ireland limited - dimethyl fumarate - multiple sclerosis, relapsing-remitting - immunosuppressants - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Caspofungin Mylan 50 mg powder for concentrate for solution for infusion Malta - English - Medicines Authority

caspofungin mylan 50 mg powder for concentrate for solution for infusion

mylan pharmaceuticals limited damastown industrial park mulhuddart dublin15 dublin, ireland - powder for concentrate for solution for infusion - caspofungin acetate 50 mg - antimycotics for systemic use

Caspofungin Mylan Pdr/Conc/Soln for Infus 70mg Malta - English - Medicines Authority

caspofungin mylan pdr/conc/soln for infus 70mg

mylan pharmaceuticals limited damastown industrial park mulhuddart dublin15 dublin, ireland - powder for concentrate for solution for infusion - caspofungin acetate 75.6 mg - antimycotics for systemic use

MYLAN-CILAZAPRIL TABLET Canada - English - Health Canada

mylan-cilazapril tablet

mylan pharmaceuticals ulc - cilazapril (cilazapril monohydrate) - tablet - 1mg - cilazapril (cilazapril monohydrate) 1mg - angiotensin-converting enzyme inhibitors

MYLAN-CILAZAPRIL TABLET Canada - English - Health Canada

mylan-cilazapril tablet

mylan pharmaceuticals ulc - cilazapril (cilazapril monohydrate) - tablet - 2.5mg - cilazapril (cilazapril monohydrate) 2.5mg - angiotensin-converting enzyme inhibitors

MYLAN-CILAZAPRIL TABLET Canada - English - Health Canada

mylan-cilazapril tablet

mylan pharmaceuticals ulc - cilazapril (cilazapril monohydrate) - tablet - 5.0mg - cilazapril (cilazapril monohydrate) 5.0mg - angiotensin-converting enzyme inhibitors