rivaroxaban accord
accord healthcare s.l.u. - rivaroxaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - Αντιθρομβωτικοί παράγοντες - Πρόληψη φλεβικής θρομβοεμβολής (vte) σε ενήλικες ασθενείς που υποβάλλονται σε εκλεκτική χειρουργική επέμβαση αντικατάστασης ισχίου ή γόνατος. Θεραπεία της φλεβικής θρόμβωσης (ΕΒΦΘ) και της πνευμονικής εμβολής (πε), και πρόληψη υποτροπιάζουσας ΕΒΦΘ και πε σε ενήλικες. (see section 4. 4 for haemodynamically unstable pe patients. Θεραπεία της φλεβικής θρόμβωσης (ΕΒΦΘ) και της πνευμονικής εμβολής (πε), και πρόληψη υποτροπιάζουσας ΕΒΦΘ και πε σε ενήλικες. (see section 4. 4 για αιμοδυναμικά ασταθής pe ασθενείς). 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. Θεραπεία της φλεβικής θρόμβωσης (ΕΒΦΘ) και της πνευμονικής εμβολής (πε), και πρόληψη υποτροπιάζουσας ΕΒΦΘ και πε σε ενήλικες. (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 και 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. Θεραπεία της φλεβικής θρόμβωσης (ΕΒΦΘ) και της πνευμονικής εμβολής (πε), και πρόληψη υποτροπιάζουσας ΕΒΦΘ και πε σε ενήλικες. (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)
mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - Αντιθρομβωτικοί παράγοντες - 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.
fucidin 1% ey.dro.sus
leo pharmaceutical products hellas ltd - fusidic acid - ΟΦΘΑΛΜΙΚΕΣ ΣΤΑΓΟΝΕΣ, ΕΝΑΙΩΡΗΜΑ - 1% - ΦΑΡΜΑΚΕΥΤΙΚΟ ΠΡΟΪΟΝ
fucidin 1% w/w (1 δόση) ey.dro.sus
leo pharmaceutical products hellas ltd - fusidic acid - ΟΦΘΑΛΜΙΚΕΣ ΣΤΑΓΟΝΕΣ, ΕΝΑΙΩΡΗΜΑ - 1% w/w (1 Δόση) - ΦΑΡΜΑΚΕΥΤΙΚΟ ΠΡΟΪΟΝ
ufexil 2mg/ml solution for infusion
demo s.a. (0000003568) 21st km national road athens-lamia, krioneri, attiki, 14568 - ciprofloxacin lactate - solution for infusion - 2mg/ml - ciprofloxacin lactate (8000002398) 2,54mg - ciprofloxacin
innohep inj.sol 20000 anti xa iu/2ml vial
ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΜΟΝΟΠΡΟΣΩΠΗ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ Δ.Τ. ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΑΕ / leo pharmaceutical hellas s.a. Παπανικολή 22a, 152 32 Χαλάνδρι 212 2225000 - tinzaparin sodium - inj.sol (ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ) - 20000 anti xa iu/2ml vial - tinzaparin sodium 10.000iu - tinzaparin
innohep inj.sol 4500antixa iu/0,45ml pf.syr
ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΜΟΝΟΠΡΟΣΩΠΗ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ Δ.Τ. ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΑΕ / leo pharmaceutical hellas s.a. Παπανικολή 22a, 152 32 Χαλάνδρι 212 2225000 - tinzaparin sodium - inj.sol (ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ) - 4500antixa iu/0,45ml pf.syr - tinzaparin sodium 10.000iu - tinzaparin
innohep 2500antixa iu/0,25ml pf.syr ενεσιμο διαλυμα
ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΑΝΩΝΥΜΗ ΕΤΑΙΡΕΙΑ Δ.Τ. ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΑΕ & leo pharmaceutical hellas sa - Τinzaparin sodium - ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ - 2500antixa iu/0,25ml pf.syr - ineof00309 - tinzaparin sodium - 10000.000000 iu - tinzaparin
innohep inj.sol 3500antixa iu/0,35ml pf.syr
ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΜΟΝΟΠΡΟΣΩΠΗ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ Δ.Τ. ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΑΕ / leo pharmaceutical hellas s.a. Παπανικολή 22a, 152 32 Χαλάνδρι 212 2225000 - tinzaparin sodium - inj.sol (ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ) - 3500antixa iu/0,35ml pf.syr - tinzaparin sodium 10.000iu - tinzaparin
innohep inj.sol 10000anti-xaiu/0,5ml pf.syr
ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΜΟΝΟΠΡΟΣΩΠΗ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ Δ.Τ. ΛΕΟ ΦΑΡΜΑΚΕΥΤΙΚΗ ΕΛΛΑΣ ΑΕ / leo pharmaceutical hellas s.a. Παπανικολή 22a, 152 32 Χαλάνδρι 212 2225000 - tinzaparin sodium - inj.sol (ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ) - 10000anti-xaiu/0,5ml pf.syr - tinzaparin sodium 20.000iu - tinzaparin