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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 (human albumin) as the active ingredient; the specific strength is not disclosed. Marketed in the European Union, this prescription‑only product is used to restore plasma volume and protein levels in clinical settings. It is administered intravenously under medical supervision. It is supplied in single‑use vials and stored at controlled temperature to maintain protein integrity.

Manufacturer / TM Owner

Csl Behring Gmbh

1
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Indications & Clinical Uses

Human Albumin Csl Behring is indicated for clinical situations that require rapid plasma volume expansion or correction of low albumin levels.

  • Treatment of hypovolemia associated with trauma, surgery, or dehydration.
  • Management of shock and severe burns where fluid loss is extensive.
  • Replacement of plasma proteins during massive transfusion or plasma exchange.
  • Support of patients with hypoalbuminemia due to liver disease, nephrotic syndrome, or malnutrition.
  • Adjunct therapy during cardiac surgery or organ transplantation to maintain oncotic pressure.

How It Works

  • Human albumin increases the oncotic pressure of the intravascular compartment by contributing to the plasma protein pool. The added albumin draws water from the interstitial space into the bloodstream, thereby expanding circulating volume. This effect helps to restore hemodynamic stability and supports transport of endogenous substances, such as hormones and drugs, that bind to albumin. The increase in oncotic pressure also reduces capillary leakage and supports endothelial integrity.

Side Effects

Adverse reactions to Human Albumin Csl Behring are generally infrequent but may occur following intravenous administration.

Common

  • Mild fever or chills during infusion.
  • Transient headache or dizziness.
  • Nausea or mild gastrointestinal discomfort.
  • Localized erythema or swelling at the injection site.

Serious

  • Anaphylactic or severe allergic reactions, including urticaria and bronchospasm.
  • Volume overload leading to pulmonary edema, especially in patients with cardiac dysfunction.
  • Hemolysis or renal impairment in susceptible individuals.
  • Transmission of infectious agents, although risk is minimized by manufacturing controls.

Precautions & Warnings

Healthcare professionals should evaluate patient history and clinical status before administering Human Albumin Csl Behring.

  • Assess for known hypersensitivity to albumin or any component of the formulation.
  • Evaluate cardiac, renal, and hepatic function to avoid volume overload.
  • Use caution in patients with active bleeding or coagulopathy, as albumin may affect clotting factors.
  • Monitor vital signs and fluid balance during and after infusion.
  • Adjust dose or infusion rate in elderly or critically ill patients.
  • Avoid use in patients with severe hypervolemia or uncontrolled hypertension.

Avoid Interactions

Human Albumin Csl Behring may interact with other therapies that influence fluid balance, coagulation, or immune response.

Avoid

  • Concurrent administration of high‑dose diuretics without careful monitoring, which can exacerbate hypovolemia.
  • Simultaneous use of other plasma expanders or colloids that may increase the risk of volume overload.
  • Blood products containing incompatible antibodies that could trigger hemolytic reactions.

Use with caution

  • Vasopressors or inotropic agents, as rapid volume changes may alter hemodynamic response.
  • Anticoagulants (e.g., heparin, warfarin) because albumin can affect plasma protein binding.
  • Immunosuppressive drugs, given the potential for altered immune modulation.
  • Renal replacement therapies, where fluid shifts need close observation.

Frequently Asked Questions

It is primarily used to expand intravascular plasma volume in patients with hypovolemia, shock, severe burns, or significant plasma protein loss.

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 specific dosing guidelines provided by the prescribing physician.

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

The manufacturing process includes viral inactivation steps, but a minimal residual risk of infectious agent transmission remains.

The infusion should be stopped immediately, and appropriate emergency treatment, such as antihistamines or epinephrine, should be administered.

Concurrent high‑dose diuretics should be avoided or used with close monitoring to prevent excessive fluid loss.

Albumin can bind various drugs; therefore, plasma protein binding and drug levels may be altered and should be monitored.

The solution should be stored at controlled refrigerated temperatures as indicated on the label to preserve protein stability.

No, it is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

Common side effects include mild fever, chills, headache, nausea, and localized injection‑site reactions.

It should be avoided in patients with known hypersensitivity to albumin, severe hypervolemia, or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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