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Reno-ALB 20% is a nonpyrogenic, sterile aqueous solution of Human Albumin I.P. for intravenous administration and is purified from pooled human venous plasma using a series of chromatography steps.
Each 100 mL RENO-ALB 20 % vial contains.
RENO-ALB 20% is produced from pooled human plasma for fractionation conforming to the highest standards set forth by regulatory authorities. In addition, the plasma donor units and the production plasma pool are tested negative using NAT approved by regulatory authorities for HIV1& 2, HCV and HBV.
Human Albumin I.P. 20% is administered intravenously. The total dosage will vary with the individual. In adults, an initial infusion of 100 mL is suggested. Additional amounts may be administered as clinically indicated. Intravenous Use Only. Human Albumin I.P. 20%, particularly if administered rapidly, may result in vascular overload with resultant pulmonary edema.
Daily dose should not exceed 2 g per kg body weight. Do not dilute with sterile water for injection as this may cause hemolysis in recipients. Large volumes and rapid infusion may cause signs and symptoms of hypervolaemia. Stop the infusion immediately. Reconstitute with 0.9% Sodium Chloride or 5% Dextrose in Water. Do not use Sterile Water for Injection as a diluent. Do not freeze.
Three years from the date of manufacturing at recommended storage conditions.
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