Europska Unija - hrvatski - EMA (European Medicines Agency)

csl behring gmbh - Коагуляционного faktora osoba viii, faktor Виллебранда osobe - hemophilia a; von willebrand diseases - blood coagulation factors, von willebrand factor and coagulation factor viii in combination, antihemorrhagics - bolest Виллебранда (vwd)prevencija i liječenje krvarenja ili kirurških krvarenja u bolesnika s vwd, kada Десмопрессин (ddavp) je jedan liječenje neučinkovito ili je kontraindicirano. hemofilija u (urođeni faktor viii vrste insuficijencije)prevencija i liječenje krvarenja u bolesnika s гемофилией a.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

baxalta innovations gmbh, industriestrasse 67, beč, austrija - адррес proteini ljudske plazme koji djeluju protiv inhibitora koagulacijskog faktora viii u - prašak i otapalo za otopinu za infuziju - 25 u/ml - urbroj: 1 ml sadrži 25 u aktivnosti protiv inhibitora koagulacijskog faktora viii 1 bočica sadrži 500 u aktivnosti protiv inhibitora koagulacijskog faktora viii u 200 – 600 mg proteina ljudske plazme

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

baxalta innovations gmbh, industriestrasse 67, beč, austrija - адррес proteini ljudske plazme koji djeluju protiv inhibitora koagulacijskog faktora viii u - prašak i otapalo za otopinu za infuziju - 50 u/ml - urbroj: 1 ml sadrži 50 u aktivnosti protiv inhibitora koagulacijskog faktora viii. feiba 50 u/ml dostupna je u tri različita pakiranja: - pakiranje od 500 u feiba sadrži 500 u aktivnosti protiv inhibitora koagulacijskog faktora viii u 200 – 600 mg proteina ljudske plazme - pakiranje od 1000 u feiba sadrži 1000 u aktivnosti protiv inhibitora koagulacijskog faktora viii u 400 – 1200 mg proteina ljudske plazme - pakiranje od 2500 u feiba sadrži 2500 u aktivnosti protiv inhibitora koagulacijskog faktora viii u 1000 – 3000 mg proteina ljudske plazme

Europska Unija - hrvatski - EMA (European Medicines Agency)

laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - antihemorrhagics - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.

Europska Unija - hrvatski - EMA (European Medicines Agency)

sanquin plasma products b.v. - faktor humanog koagulacije ix - hemofilija b - antihemorrhagics - liječenje i profilaksu krvarenja u bolesnika s hemofilijom b (nedostatak prirođenog faktora ix).

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

biomedica dijagnostika d.o.o. paljetkova 2 10000 zagreb -

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

biomedica dijagnostika d.o.o. paljetkova 2 10000 zagreb -

Europska Unija - hrvatski - EMA (European Medicines Agency)

bpl bioproducts laboratory gmbh - ljudski faktor zgrušavanja x - nedostatak faktora x - vitamin k and other hemostatics, antihemorrhagics, coagulation factor x - coagadex je indiciran za liječenje i profilaksu epizoda krvarenja i za perioperativno liječenje u bolesnika s nedostatkom nasljednog faktora x. coagadex navedeno je u svim dobnim skupinama.

Europska Unija - hrvatski - EMA (European Medicines Agency)

bayer ag - rivaroksaban - arthroplasty, replacement; venous thromboembolism - antitrombotska sredstva - xarelto, uvedene zajedno sa ацетилсалициловой kiselinom (ask) sami ili sa asc plus клопидогрел ili Тиклопидин, prikazana za prevenciju атеротромботических događaja kod odraslih pacijenata nakon akutnog koronarni sindrom (acs) s povišenom razinom кардиальных biomarkera. xarelto, 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. prevencija venske tromboembolije (vte) u odraslih bolesnika koji se podvrgavaju izborni operacije zamjena kuka ili koljena. liječenje tromboze dubokih vena (dvt) i plućne embolije (ТЭЛА) i prevenciju recidiva dvt i ТЭЛА kod odraslih. adultsprevention 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.

Europska Unija - hrvatski - EMA (European Medicines Agency)

accord healthcare s.l.u. - rivaroksaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - antitrombotska sredstva - prevencija venske tromboembolije (vte) u odraslih bolesnika koji se podvrgavaju izborni operacije zamjena kuka ili koljena. liječenje tromboze dubokih vena (dvt) i plućne embolije (ТЭЛА) i prevenciju recidiva dvt i ТЭЛА kod odraslih. (see section 4. 4 for haemodynamically unstable pe patients. liječenje tromboze dubokih vena (dvt) i plućne embolije (ТЭЛА) i prevenciju recidiva dvt i ТЭЛА kod odraslih. (see section 4. 4 za hemodinamski nestabilne ТЭЛА pacijenata). adultsprevention 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. liječenje tromboze dubokih vena (dvt) i plućne embolije (ТЭЛА) i prevenciju recidiva dvt i ТЭЛА kod odraslih. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment 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. rivaroxaban accord, co administered with acetylsalicylic acid (asa) alone or with asa plus ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers (see sections 4. 3, 4. 4 i 5. rivaroxaban accord, 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. adultsprevention 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. liječenje tromboze dubokih vena (dvt) i plućne embolije (ТЭЛА) i prevenciju recidiva dvt i ТЭЛА kod odraslih. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment 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.