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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 solution for injection that contains human plasma protein as the active ingredient. It is supplied as a liquid formulation without a specified strength, intended for intravenous administration. The product is classified as a plasma volume expander and is available by prescription in the European Union market.

Manufacturer / TM Owner

Csl Behring Gmbh

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Indications & Clinical Uses

Human Albumin CSL Behring is used in clinical settings to restore and maintain circulating blood volume. It is indicated for conditions where plasma oncotic pressure is reduced or where rapid volume expansion is required.

  • Treatment of hypovolemia due to trauma, surgery, or fluid loss
  • Management of shock and severe burns
  • Support for patients with hypoalbuminemia, such as in liver disease
  • Volume replacement during cardiac surgery and cardiopulmonary bypass
  • Adjunct therapy in patients with severe sepsis or systemic inflammatory response

How It Works

  • Human Albumin CSL Behring increases plasma oncotic pressure by adding exogenous albumin to the intravascular compartment. The elevated oncotic gradient draws water from the interstitial space into the vascular lumen, expanding circulating blood volume and improving tissue perfusion without directly affecting cardiac contractility or vascular tone.

Side Effects

Adverse reactions to Human Albumin CSL Behring can vary in frequency and severity.

Common

  • Fever or chills
  • Mild hypotension or hypertension
  • Headache
  • Nausea or vomiting
  • Local irritation at the infusion site
  • Transient rash or urticaria

Serious

  • Anaphylactic or severe allergic reactions
  • Acute hemolysis
  • Pulmonary edema due to fluid overload
  • Thromboembolic events
  • Severe hypertension or cardiovascular collapse

Precautions & Warnings

Human Albumin CSL Behring should be administered with careful clinical assessment. Consider the following precautions:

  • Evaluate fluid status and cardiac function before infusion
  • Monitor vital signs and urine output during and after administration
  • Use caution in patients with renal or hepatic impairment
  • Avoid rapid infusion rates to reduce risk of circulatory overload
  • Assess for known hypersensitivity to human albumin products
  • Adjust dose in patients with severe burns or capillary leak syndrome
  • Document any adverse reactions promptly

Avoid Interactions

Human Albumin CSL Behring may interact with other therapies that affect fluid balance or coagulation.

Avoid

  • Concurrent use of high‑dose diuretics without monitoring volume status
  • Simultaneous administration of other plasma expanders that could cause overload

Use with caution

  • Vasopressor agents, as changes in intravascular volume may alter hemodynamic response
  • Anticoagulants, because volume expansion can affect bleeding risk
  • Steroids or immunosuppressants, which may mask allergic reactions
  • Blood products, to prevent additive volume overload
  • Medications that influence renal function, requiring close monitoring

Frequently Asked Questions

It is used as a plasma volume expander to treat hypovolemia, shock, severe burns, hypoalbuminemia, and to support patients during cardiac surgery or liver disease.

The product is supplied as a sterile solution for injection and is administered intravenously under medical supervision.

Use in children should be based on clinical judgment and dosing guidelines provided by the prescribing physician, taking into account the child's weight and condition.

Vital signs, urine output, and signs of fluid overload should be monitored before, during, and after the infusion.

Yes, hypersensitivity reactions can occur; clinicians should be prepared to manage anaphylaxis if it arises.

Symptoms may include shortness of breath, pulmonary edema, elevated blood pressure, and swelling of the extremities.

Diuretics may need adjustment; clinicians should evaluate fluid status and coordinate diuretic therapy to avoid excessive volume shifts.

It can be administered alongside blood products, but careful monitoring is required to prevent volume overload.

Human Albumin raises plasma oncotic pressure, drawing water from the interstitial space into the bloodstream, thereby increasing circulating volume.

The product is marketed in the European Union; approval status in other regions should be confirmed with local regulatory agencies.

It should be stored according to the manufacturer’s instructions, typically refrigerated and protected from light, and used before the expiration date.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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