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Human Albumin Csl Behring

Active Ingredient:
Human Plasma Protein
Origin:
EU

Human Albumin Csl Behring (Human Plasma Protein)

Human Albumin Csl Behring is a sterile intravenous solution containing human albumin, a plasma protein, supplied in a standard concentration (e.g., 20% w/v) for clinical use. It is manufactured in the European Union and prescribed by healthcare professionals as a volume expander to restore and maintain circulatory volume in patients with hypoalbuminemia or acute blood loss. The product is administered under medical supervision and stored according to label instructions.

Manufacturer / TM Owner

Csl Behring Gmbh

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Indications & Clinical Uses

Human Albumin Csl Behring is employed clinically as a volume expander and protein replacement in several medical situations where plasma albumin levels are low or rapid fluid shifts occur.

  • Management of hypovolemia due to acute blood loss or trauma.
  • Treatment of hypoalbuminemia associated with liver cirrhosis or nephrotic syndrome.
  • Support during major surgery or extensive burns to maintain oncotic pressure.
  • Adjunct therapy in patients receiving parenteral nutrition with low serum albumin.
  • Correction of dilutional coagulopathy in massive transfusion protocols.

How It Works

  • Human albumin increases plasma oncotic pressure by contributing to the colloid osmotic gradient within the vascular compartment. The infused protein binds water, drawing fluid from the interstitial space into the circulation, thereby expanding intravascular volume. This effect helps restore hemodynamic stability and supports tissue perfusion. Albumin also serves as a carrier for endogenous substances such as hormones, fatty acids, and drugs, influencing their distribution.

Side Effects

Adverse reactions to Human Albumin Csl Behring are generally infrequent but may range from mild to severe.

Common

  • Transient fever or chills.
  • Mild hypotension or hypertension.
  • Headache or dizziness.

Serious

  • Anaphylactic or severe allergic reaction.
  • Pulmonary edema from volume overload.
  • Acute respiratory distress syndrome (ARDS).

Precautions & Warnings

When prescribing Human Albumin Csl Behring, clinicians should evaluate patient-specific factors and monitor for potential complications.

  • Assess volume status to avoid fluid overload.
  • Use caution in patients with heart failure or renal insufficiency.
  • Monitor serum albumin and electrolytes during therapy.
  • Adjust dose in patients with severe hypoalbuminemia.
  • Avoid rapid infusion rates; infuse over recommended time.
  • Discontinue if signs of allergic reaction appear.

Avoid Interactions

Human Albumin may interact with other agents that affect fluid balance, coagulation, or immune response.

Avoid

  • Concomitant use of high‑dose diuretics that may exacerbate hypovolemia.
  • Simultaneous administration of other volume expanders without careful monitoring.
  • Use with agents that increase risk of pulmonary edema (e.g., excessive crystalloid fluids).

Use with caution

  • Blood products or plasma derivatives that may increase oncotic load.
  • Medications that bind albumin (e.g., warfarin, phenytoin) as they may alter drug levels.
  • Immunosuppressive therapies that could mask allergic reactions.

Frequently Asked Questions

Human Albumin Csl Behring is a sterile intravenous solution that contains purified human albumin, typically provided in a 20% w/v concentration for infusion.

It is indicated for volume expansion in hypovolemia, treatment of hypoalbuminemia due to liver or kidney disease, support during major surgery or burns, and as adjunct therapy in massive transfusion protocols.

Albumin contributes to the colloid osmotic gradient, binding water and pulling fluid from the interstitial space into the vascular compartment, thereby raising intravascular oncotic pressure.

Common reactions include transient fever or chills, mild changes in blood pressure, and headache or dizziness during or shortly after infusion.

Serious complications may include anaphylactic or severe allergic reactions, pulmonary edema from volume overload, and acute respiratory distress syndrome (ARDS).

Patients should be monitored for vital signs, fluid balance, serum albumin levels, electrolytes, and any signs of allergic reaction throughout the infusion and afterward.

Contraindications include known hypersensitivity to albumin preparations and conditions where fluid overload would be hazardous, such as uncontrolled heart failure.

Drugs that bind albumin (e.g., warfarin, phenytoin) may have altered plasma concentrations, and high‑dose diuretics can exacerbate hypovolemia when used together.

The infusion is usually administered slowly, often over 30–60 minutes, with the rate adjusted based on patient tolerance and clinical response.

The product should be stored at controlled room temperature, protected from light, and used before the expiration date indicated on the label.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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