FLEXBUMIN 5% and 25% are indicated for hypovolemia, hypoalbuminemia (burns), and cardiopulmonary bypass surgery. Albumin is not indicated as an intravenous nutrient. FLEXBUMIN 25% is also indicated for hypoalbuminemia due to Adult Respiratory Distress Syndrome (ARDS) and nephrosis, and for hemolytic disease of the newborn (HDN).
FLEXBUMIN is the first human albumin in
a flexible, shatterproof container.1-3*
* FLEXBUMIN 25% Solution was FDA approved on
October 11, 2005.
Delivered with no extra packaging, FLEXBUMIN in the GALAXY container is designed to maintain sterility during setup and administration.1-5
Delivered in a shatterproof, flexible container, FLEXBUMIN helps reduce risk in critical situations.1-8
Lightweight and flexible, the FLEXBUMIN container helps enhance storage and setup efficiencies.1-3,9-10
Delivered in a lightweight, flexible container, FLEXBUMIN helps reduce environmental impacts throughout the product lifecycle.1-3,10-12†
†Calculations based on BUMINATE® [Albumin (Human)], USP, 5% and 25% Solutions in glass bottles of equal volume.
References
Indications and Limitation of Use
FLEXBUMIN [Albumin (Human)] 5% and 25% are indicated for hypovolemia, hypoalbuminemia (burns), and cardiopulmonary bypass surgery. Albumin is not indicated as an intravenous nutrient. FLEXBUMIN 25% is also indicated for hypoalbuminemia due to Adult Respiratory Distress Syndrome (ARDS) and nephrosis, and for hemolytic disease of the newborn (HDN).
Important Safety Information
Contraindications