VONILLE 60 micrograme/15 micorgrame Romunija - romunščina - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

vonille 60 micrograme/15 micorgrame

ladeepharma kft - combinatii (gestodenum+etinilestradiolum) - compr. film. - 60micrograme/15micorgrame - contraceptive hormonale pentru uz sistemic progesteroni si estrogeni combinatii fixe

FOSTER NEXTHALER 200 micrograme/6 micrograme Romunija - romunščina - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

foster nexthaler 200 micrograme/6 micrograme

chiesi farmaceutici s.p.a. - italia - combinatii (beclometasonum+formoterolum) - pulb. de inhal. - 200micrograme/6micrograme - adrenergice inhalante adrenergice si alte med. pt. trat. bolilor obstructive c.r

Arixtra Evropska unija - romunščina - EMA (European Medicines Agency)

arixtra

mylan ire healthcare limited - fondaparinux sodic - venous thrombosis; pulmonary embolism; myocardial infarction; angina, unstable - agenți antitrombotici - 5 mg / 0. 3 ml și 2. 5 mg / 0. 5-ml solution for injectionprevention of venous thromboembolic events (vte) in adults undergoing major orthopaedic surgery of the lower limbs such as hip fracture, major knee surgery or hip-replacement surgery. prevenirea tev la adulți supuși unei intervenții chirurgicale abdominale considerați a avea risc înalt de complicații tromboembolice, cum ar fi pacienții supuși unei intervenții chirurgicale pentru cancer abdominal. prevenirea tev la pacienții adulți medicale care sunt considerate a fi la mare risc pentru tev și care sunt imobilizați datorită unor boli acute cum ar fi insuficiență cardiacă și / sau respiratorie acută tulburări, și / sau boli infecțioase sau inflamatorii acute. tratamentul adulților cu simptomatologie acută spontane superficiale-tromboza venoasă a membrelor inferioare, fără administrare concomitentă de tromboză. 5 mg / 0. 5-ml solution for injectiontreatment of unstable angina or non-st-segment-elevation myocardial infarction (ua/nstemi) in adult patients for whom urgent (< 120 mins) invasive management (pci) is not indicated. miocardic acut (stemi) la pacienții adulți care sunt tratați cu trombolitice sau care inițial vor primi nici o altă formă de terapie de reperfuzie. 5 mg / 0. 4-ml, 7. 5 mg / 0. 6-ml și 10 mg/0. 8-ml solution for injectiontreatment of adults with acute deep-vein thrombosis (dvt) and treatment of acute pulmonary embolism (pe), except in haemodynamically unstable patients or patients who require thrombolysis or pulmonary embolectomy.

Rivaroxaban Viatris (previously Rivaroxaban Mylan) Evropska unija - romunščina - 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 - agenți antitrombotici - 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.

VELBIENNE 2 mg/1 mg Romunija - romunščina - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

velbienne 2 mg/1 mg

ladeepharma kft. - combinatii (dienogestum+etinilestradiolum) - compr. film. - 2mg/1mg - combinatii de hormoni progestogeni si estrogeni progestative si estrogeni, combinatii fixe