Plasbumin 20

About Plasbumin 20

Grifols Human Albumin I.P. 20% Injection is a sterile, non-pyrogenic solution of human albumin prepared from human plasma using advanced fractionation and purification techniques. It is widely used for plasma volume expansion and maintenance of colloid osmotic pressure in patients with hypovolemia and hypoalbuminemia.

This high-purity albumin solution is manufactured following stringent quality and safety standards to ensure maximum efficacy and patient safety.

Uses / Indications

• Treatment of hypovolemia

• Management of hypoalbuminemia

• Plasma volume replacement

• Supportive therapy in liver failure

• Burns and trauma cases

• Major surgical procedures

• Nephrotic syndrome (as prescribed)

Key Benefits

• High-purity, plasma-derived human albumin

• Helps restore and maintain blood volume

• Maintains oncotic pressure

• Low risk of adverse reactions

• Manufactured under strict GMP standards

Dosage & Administration

Dosage and infusion rate should be determined by the physician based on the patients clinical condition, body weight, and response to treatment.

Storage Instructions

• Store below 25C

• Do not freeze

• Protect from light

• Use immediately after opening

Benefits and Applications of Plasbumin 20

Plasbumin 20 is renowned for its effectiveness in managing hypovolemia, addressing hypoalbuminemia, supporting patients with burn injuries, and aiding in procedures like cardiopulmonary bypass. Its rapid restoration of plasma volume helps stabilize patients quickly, while its high purity and viral safety offer peace of mind for medical professionals and patients alike.


Safe Storage and Shelf Life

Store Plasbumin 20 between 2C to 8C, away from light and never frozen, to maintain product integrity. Each vial is single-use, ensuring sterility and reducing contamination risks. Once opened, use the solution within 24 hours to ensure maximum efficacy and safety for patients.


Viral Safety and Purity

Every batch of Plasbumin 20 undergoes thorough viral inactivation, including pasteurization, to eliminate potential pathogens. This guarantees a product free from preservatives and pyrogens, making it suitable for critical clinical applications requiring high safety standards. Its manufacturing process aligns with international quality norms.