Steri-Tamp™ tamper evident seals Israel - Hebräisch - Ministry of Health

steri-tamp™ tamper evident seals

"דין ציוד רפואי בע""מ" - אחר - "לשימוש במוסדות רפואיים מרפאות, בתי חולים ,בתי מרקחת ומוסדות סיעודיים"

Steri-Tamp™ tamper evident seals Israel - Hebräisch - Ministry of Health

steri-tamp™ tamper evident seals

דין ציוד רפואי - אחר - לשימוש במוסדות רפואיים מרפאות, בתי חולים ,בתי מרקחת ומוסדות סיעודיים

בספונסה Israel - Hebräisch - Ministry of Health

בספונסה

pfizer pharmaceuticals israel ltd - inotuzumab ozogamicin - אבקה להכנת תמיסה מרוכזת לעירוי - inotuzumab ozogamicin 1 mg/vial - inotuzumab ozogamicin

מיילוטארג Israel - Hebräisch - Ministry of Health

מיילוטארג

pfizer pharmaceuticals israel ltd - gemtuzumab ozogamicin - אבקה להכנת תמיסה מרוכזת לעירוי - gemtuzumab ozogamicin 5 mg/vial - gemtuzumab

זיראבוו Israel - Hebräisch - Ministry of Health

זיראבוו

pfizer pharmaceuticals israel ltd - bevacizumab - תרכיז להכנת תמיסה לאינפוזיה - bevacizumab 25 mg / 1 ml - bevacizumab

יורוציט-קיי 10 mEq Israel - Hebräisch - Ministry of Health

יורוציט-קיי 10 meq

pharmabest import (2003) ltd, israel - potassium citrate - טבליות עם שחרור נרחב - potassium citrate 1080 mg - potassium citrate

רמסימה 100 מג תוך-ורידי Israel - Hebräisch - Ministry of Health

רמסימה 100 מג תוך-ורידי

padagis israel agencies ltd, israel - infliximab - אבקה להכנת תמיסה מרוכזת לעירוי - infliximab 100 mg/vial - infliximab

אללייזו Israel - Hebräisch - Ministry of Health

אללייזו

pfizer pharmaceuticals israel ltd - taliglucerase alfa - אבקה להכנת תמיסה לאינפוזיה - taliglucerase alfa 200 u/vial - taliglucerase alfa - taliglucerase alfa - elelyso (taliglucerase alfa ) for injection is a hydrolytic lysosomal glucocerebroside - specific enzyme indicated for long - term enzyme replacement therapy (ert) for adults with a confirmed diagnosis of type 1 gaucher disease.

בינוקריט 1000 יחבל 0.5 מל Israel - Hebräisch - Ministry of Health

בינוקריט 1000 יחבל 0.5 מל

novartis israel ltd - epoetin alfa - תמיסה להזרקה - epoetin alfa 1000 iu / 0.5 ml - erythropoietin - erythropoietin - 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). binocrit 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 non-iron deficient patients with moderate anaemia (haemoglob

בינוקריט 2000 יחבל 1 מל Israel - Hebräisch - Ministry of Health

בינוקריט 2000 יחבל 1 מל

novartis israel ltd - epoetin alfa - תמיסה להזרקה - epoetin alfa 2000 iu / 1 ml - erythropoietin - erythropoietin - 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). binocrit 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 non-iron deficient patients with moderate anaemia (haemoglob