EPORATIO 30,000 IU Israel - English - Ministry of Health

eporatio 30,000 iu

salomon,levin & elstein ltd - epoetin theta (r-huepo) 30000 iu / 1 ml - solution for injection - erythropoietin - - treatment of symptomatic anaemia associated with chronic renal failure in adult patients.- treatment of symptomatic anaemia in adult cancer patients with non-myeloid malignancies receiving chemotherapy.

Recormon Pre-filled Syringe 30000 iu0.6 ml Singapore - English - HSA (Health Sciences Authority)

recormon pre-filled syringe 30000 iu0.6 ml

roche singapore pte. ltd. - epoetin beta - injection, solution - 30,000 iu - epoetin beta 30,000 iu/0.6 ml

RECORMON PRE-FILLED SYRINGE 4000 iu0.3 ml Singapore - English - HSA (Health Sciences Authority)

recormon pre-filled syringe 4000 iu0.3 ml

roche singapore pte. ltd. - epoetin beta - injection - 4000 iu/0.3 ml - epoetin beta 4000 iu/0.3 ml

RECORMON PRE-FILLED SYRINGE 6000 iu/0.3 ml Singapore - English - HSA (Health Sciences Authority)

recormon pre-filled syringe 6000 iu/0.3 ml

roche singapore pte. ltd. - epoetin beta - injection - 6000 iu/0.3 ml

RECORMON PRE-FILLED SYRINGE 10000 iu0.6 ml Singapore - English - HSA (Health Sciences Authority)

recormon pre-filled syringe 10000 iu0.6 ml

roche singapore pte. ltd. - epoetin beta - injection - 10000 iu/0.6 ml - epoetin beta 10000 iu/0.6 ml

RECORMON PRE-FILLED SYRINGE 2000 iu0.3 ml Singapore - English - HSA (Health Sciences Authority)

recormon pre-filled syringe 2000 iu0.3 ml

roche singapore pte. ltd. - epoetin beta - injection - 2000 iu/0.3 ml - epoetin beta 2000 iu/0.3 ml

RECORMON PRE-FILLED SYRINGE 3000 iu/0.3 ml Singapore - English - HSA (Health Sciences Authority)

recormon pre-filled syringe 3000 iu/0.3 ml

roche singapore pte. ltd. - epoetin beta - injection - 3000 iu/0.3 ml

RECORMON PRE-FILLED SYRINGE 5000 iu/0.3 ml Singapore - English - HSA (Health Sciences Authority)

recormon pre-filled syringe 5000 iu/0.3 ml

roche singapore pte. ltd. - epoetin beta - injection - 5000 iu/0.3 ml

Abseamed European Union - English - EMA (European Medicines Agency)

abseamed

medice arzneimittel pütter gmbh co. kg - epoetin alfa - anemia; kidney failure, chronic; cancer - antianemic preparations - treatment of symptomatic anaemia associated with chronic renal failure (crf) in adult and paediatric patients:treatment of anaemia associated with chronic renal failure in paediatric and adult patients on haemodialysis and adult patients on peritoneal dialysis;treatment of severe anaemia of renal origin accompanied by clinical symptoms in adult patients with renal insufficiency not yet undergoing dialysis.treatment of anaemia and reduction of transfusion requirements in adult patients receiving chemotherapy for solid tumours, malignant lymphoma or multiple myeloma, and at risk of transfusion as assessed by the patient's general status (e.g. cardiovascular status, pre existing anaemia at the start of chemotherapy).abseamed can be used to increase the yield of autologous blood from patients in a predonation programme. its use in this indication must be balanced against the reported risk of thromboembolic events. treatment should only be given to patients with moderate anaemia (haemoglobin (hb) 10-13 g/dl [6.2-8.1 mmol/l], no iron deficiency), if blood saving procedures are not available or insufficient when the scheduled major elective surgery requires a large volume of blood (4 or more units of blood for females or 5 or more units for males).abseamed can be used to reduce exposure to allogeneic blood transfusions in adult non iron deficient patients prior to major elective orthopaedic surgery, having a high perceived risk for transfusion complications. use should be restricted to patients with moderate anaemia (e.g. hb 10-13 g/dl) who do not have an autologous predonation programme available and with an expected blood loss of 900 to 1800 ml.

Binocrit European Union - English - EMA (European Medicines Agency)

binocrit

sandoz gmbh - epoetin alfa - anemia; kidney failure, chronic - antianemic preparations - treatment of symptomatic anaemia associated with chronic renal failure (crf) in adult and paediatric patients: , treatment of anaemia associated with chronic renal failure in paediatric and adult patients on haemodialysis and adult patients on peritoneal dialysis;, treatment of severe anaemia of renal origin accompanied by clinical symptoms in adult patients with renal insufficiency not yet undergoing dialysis;, treatment of anaemia and reduction of transfusion requirements in adult patients receiving chemotherapy for solid tumours, malignant lymphoma or multiple myeloma, and at risk of transfusion as assessed by the patient's general status (e.g. cardiovascular status, pre-existing anaemia at the start of chemotherapy).