Product image of Human Albumin Csl Behring (Human Plasma Protein) supplied by GNH India

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 plasma protein (human albumin) as its active ingredient. The product is supplied without a disclosed strength and is intended for infusion by healthcare professionals. Classified as a plasma protein and volume expander, it is marketed in the European Union and requires a prescription. The preparation is used to restore plasma oncotic pressure in appropriate clinical settings.

Manufacturer / TM Owner

Csl Behring Gmbh

1
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Indications & Clinical Uses

Human Albumin Csl Behring is indicated for conditions where plasma volume or albumin levels need rapid restoration.

  • Treatment of hypovolemia due to acute blood loss, trauma, or dehydration.
  • Management of hypoalbuminemia associated with chronic liver disease or nephrotic syndrome.
  • Volume expansion in patients undergoing major surgery, such as cardiac or transplant procedures.
  • Supportive therapy for extensive burns to maintain intravascular oncotic pressure.
  • Adjunct in plasma exchange or therapeutic apheresis when albumin replacement is required.
  • Correction of dilutional hypoalbuminemia during massive fluid resuscitation in critical care settings.

How It Works

  • Human Albumin Csl Behring works by increasing the concentration of albumin in the intravascular compartment, which raises plasma oncotic pressure. The elevated oncotic gradient draws water from the interstitial space into the bloodstream, expanding circulating volume. Albumin also serves as a carrier protein for endogenous substances such as hormones, fatty acids, and drugs, contributing to hemodynamic stability and supporting transport functions.

Side Effects

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

Common

  • Fever or chills during infusion.
  • Mild rash or urticaria at infusion site.
  • Headache or dizziness.
  • Nausea or vomiting.
  • Transient hypotension during administration.
  • Mild itching or pruritus.
  • Elevated heart rate (tachycardia).
  • Mild swelling or edema at the infusion site.
  • Transient increase in serum calcium levels.

Serious

  • Anaphylactic or severe allergic reaction.
  • Acute respiratory distress or bronchospasm.
  • Hemolysis or renal impairment.
  • Thromboembolic events such as deep vein thrombosis.
  • Severe hypertension or hypertensive crisis.
  • Disseminated intravascular coagulation (DIC).
  • Cardiac arrest or severe arrhythmias.
  • Pulmonary edema due to rapid volume expansion.

Precautions & Warnings

When using Human Albumin Csl Behring, clinicians should observe several precautions to minimize risk and ensure appropriate patient selection.

  • Verify baseline serum albumin and volume status before administration.
  • Do not administer to patients with a documented allergy to human albumin or other plasma proteins.
  • Monitor vital signs and fluid balance closely during and after infusion to detect overload.
  • Use caution in individuals with congestive heart failure, coronary artery disease, or pulmonary hypertension.
  • Adjust dose or infusion rate in patients with renal impairment or reduced hepatic function.
  • Infuse slowly (not exceeding recommended rate) to reduce risk of hypotension and anaphylaxis.

Avoid Interactions

Human Albumin Csl Behring may interact with certain medications or clinical conditions; awareness of these interactions helps prevent adverse outcomes.

Avoid

  • Concomitant use with other volume expanders that may cause fluid overload.
  • Administration with drugs that have a high protein binding displacement risk (e.g., warfarin) may alter plasma concentrations.
  • Use with hyperoncotic agents such as dextran in the same infusion line.

Use with caution

  • Concurrent diuretics may increase risk of electrolyte imbalance.
  • Co-administration with vasopressors may require dose adjustments.
  • Patients receiving renal replacement therapy may need monitoring of albumin levels.
  • Use in combination with blood products may affect coagulation parameters.

Frequently Asked Questions

Human Albumin Csl Behring is a sterile intravenous solution whose active ingredient is human plasma protein, specifically human albumin. It is supplied as a prescription product for infusion by qualified healthcare professionals.

The product is commonly prescribed to treat hypovolemia, hypoalbuminemia, to support patients with extensive burns, during major surgeries requiring volume expansion, and as an adjunct in plasma exchange or therapeutic apheresis.

By increasing intravascular albumin concentration, the solution raises plasma oncotic pressure, drawing water from the interstitial space into the bloodstream and thereby expanding circulating volume.

No. Human Albumin Csl Behring is classified as a prescription‑only medication and must be administered under medical supervision.

The product is administered intravenously, typically through a controlled infusion set in a clinical setting.

Vital signs, fluid balance, and signs of allergic reaction should be monitored closely throughout the infusion and for a period afterward.

Use with caution. Patients with congestive heart failure may be at higher risk for fluid overload, so infusion rate and volume should be carefully managed.

Common reactions include fever, chills, mild rash or urticaria, headache, dizziness, nausea, vomiting, transient hypotension, itching, and mild swelling at the infusion site.

Serious side effects include anaphylaxis, acute respiratory distress, bronchospasm, hemolysis, renal impairment, thromboembolic events, severe hypertension, disseminated intravascular coagulation, cardiac arrest, and pulmonary edema.

Concurrent use with other volume expanders, high protein‑binding drugs such as warfarin, and hyperoncotic agents like dextran should be avoided to reduce the risk of adverse interactions.

The product should be stored according to the manufacturer’s instructions, typically refrigerated and protected from light, and used before the expiration date indicated on the label.

Patients with reduced renal function should have the infusion rate and total volume adjusted, and albumin levels should be monitored to avoid fluid overload.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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