Hemosol B0 raztopina za hemodializo/hemofiltracijo Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

hemosol b0 raztopina za hemodializo/hemofiltracijo

gambro lundia ab - kalcijev klorid dihidrat; magnezijev klorid heksahidrat; mlečna kislina; natrijev hidrogenkarbonat; natrijev klorid - raztopina za hemodializo/hemofiltracijo - kalcijev klorid dihidrat 5,145 mg / 1 ml  magnezijev klorid heksahidrat2,033 mg / 1 ml  mlečna kislina5,4 mg / 1 ml  natrijev hidrogenkarbonat3,09 mg / 1 ml  natrijev klorid6,45 mg / 1 ml; magnezijev klorid heksahidrat 2,033 mg / 1 ml  mlečna kislina5,4 mg / 1 ml  natrijev hidrogenkarbonat3,09 mg / 1 ml  natrijev klorid6,45 mg / 1 ml; mlečna kislina 5,4 mg / 1 ml  natrijev hidrogenkarbonat3,09 mg / 1 ml  natrijev klorid6,45 mg / 1 ml; natrijev hidrogenkarbonat 3,09 mg / 1 ml  natrijev klorid6,45 mg / 1 ml; natrijev klorid 6,45 mg / 1 ml - zdravila za filtracijo krvi

Rivaroxaban Accord Evropska unija - slovenščina - EMA (European Medicines Agency)

rivaroxaban accord

accord healthcare s.l.u. - rivaroksaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - antitrombotična sredstva - preprečevanje venska trombembolija (vte) pri odraslih bolnikih, ki so v postopku izbirni kirurški zamenjavi kolka ali kolena. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri odraslih. (see section 4. 4 for haemodynamically unstable pe patients. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri odraslih. (see section 4. 4 za haemodynamically nestabilno pe bolnikov). 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. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri 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 in 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. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri 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.

Rivaroxaban Viatris (previously Rivaroxaban Mylan) Evropska unija - slovenščina - 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 - antitrombotična sredstva - 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.

Xarelto Evropska unija - slovenščina - EMA (European Medicines Agency)

xarelto

bayer ag - rivaroksaban - arthroplasty, replacement; venous thromboembolism - antitrombotična sredstva - xarelto, co-daje z acetilsalicilne kisline (asa) samostojno ali s asa plus clopidogrel ali ticlopidine, je označen za preprečevanje atherothrombotic dogodkov pri odraslih bolnikih po akutni koronarni sindrom (acs) s povišano srčno biomarkerje. 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. preprečevanje venska trombembolija (vte) pri odraslih bolnikih, ki so v postopku izbirni kirurški zamenjavi kolka ali kolena. zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri 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.

Imrestor Evropska unija - slovenščina - EMA (European Medicines Agency)

imrestor

elanco gmbh - pegbovigrastim - colony stimulating factors, immunostimulants, zdravila z delovanjem na novotvorbe agenti - cattle (cows and heifers); cattle - kot pomoč v programu za črede zmanjšati tveganje za klinični mastitis v perifernih mlečnih kravah in telicah v 30 dneh po telitvi.

Jetrea Evropska unija - slovenščina - EMA (European Medicines Agency)

jetrea

inceptua ab - ocriplazmin - retinalne bolezni - oftalmologi - jetrea je indicirana pri odraslih za zdravljenje vitreomakularnega vleka (vmt), vključno s povezavo z makularno luknjo s premerom, ki je manjša od ali enaka 400 mikronov.

Vagisan 167 mg/100 mg vaginalne globule Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

vagisan 167 mg/100 mg vaginalne globule

dr. a. wolff - mlečna kislina - vaginalna globula - mlečna kislina 167 mg / 1 vag. globula - mlečna kislina