cefuroxime mylan 250 mg tabletki powlekane
mylan ireland limited - cefuroximum - tabletki powlekane - 250 mg
cefuroxime mylan 500 mg tabletki powlekane
mylan ireland limited - cefuroximum - tabletki powlekane - 500 mg
sorafenib mylan 200 mg tabletki powlekane
mylan ireland limited - sorafenibum - tabletki powlekane - 200 mg
fingolimod mylan
mylan ireland limited - fingolimod jest chlorowodorek - stwardnienie rozsiane, Рецидивно-znika - leki immunosupresyjne - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older:patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 i 5. 1)orpatients z szybko rozwija się ciężka relapsing odpuszcza stwardnieniem rozsianym jest określona przez 2 lub więcej ciężkich nawrotów w ciągu jednego roku, i z 1 lub więcej gadolin aktywizacji ognisk w mri mózgu lub znaczny wzrost obciążenia t2 porażki w porównaniu z ostatnim mri.
rivaroxaban viatris (previously rivaroxaban mylan)
mylan ireland limited - rywaroksaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - Środki przeciwzakrzepowe - 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.
sugammadex mylan
mylan ireland limited - sugammadex sodium - blokada nerwowo-mięśniowa - wszystkie inne produkty terapeutyczne - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.
fingolimod mylan
mylan ireland limited - fingolimod jest chlorowodorek - stwardnienie rozsiane, Рецидивно-znika - leki immunosupresyjne - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 i 5. 1) or patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.
eptifibatide mylan 0,75 mg/ml roztwór do infuzji
mylan s.a.s. - eptifibatidum - roztwór do infuzji - 0,75 mg/ml
eptifibatide mylan 2 mg/ml roztwór do wstrzykiwań
mylan s.a.s. - eptifibatidum - roztwór do wstrzykiwań - 2 mg/ml
fludarabine mylan 50 mg proszek do sporządzania roztworu do wstrzykiwań lub infuzji
mylan s.a.s. - fludarabini phosphas - proszek do sporządzania roztworu do wstrzykiwań lub infuzji - 50 mg