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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 prescription‑only solution for injection that contains human plasma protein (human albumin) as its active ingredient. The product is supplied in a sterile aqueous solution, with the exact concentration varying by market, and is manufactured for use in the European Union. It is classified as a plasma‑derived volume expander and is typically used in hospital settings for patients requiring rapid plasma volume restoration.

Manufacturer / TM Owner

Csl Behring Gmbh

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Indications & Clinical Uses

Human Albumin CSL Behring is indicated for clinical situations where an increase in plasma oncotic pressure and intravascular volume is required.

  • Treatment of hypovolemia due to burns, trauma, or major surgery.
  • Management of hypoalbuminemia associated with liver disease, nephrotic syndrome, or malnutrition.
  • Support during plasma exchange procedures and extracorporeal circulation.
  • Adjunct therapy for patients with severe sepsis or septic shock when fluid resuscitation is needed.
  • Volume replacement in cardiopulmonary bypass or hemodialysis when conventional crystalloids are insufficient.

How It Works

  • Human albumin acts as a natural plasma protein that contributes to oncotic pressure. When infused intravenously, it expands the intravascular compartment by drawing water from the interstitial space into the bloodstream, thereby increasing circulating volume. The added albumin also serves as a carrier for endogenous substances such as hormones, fatty acids, and drugs, supporting transport and distribution while helping maintain vascular integrity.

Side Effects

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

Common

  • Mild fever or chills during or shortly after infusion.
  • Transient hypotension or hypertension.
  • Headache or dizziness.
  • Nausea or mild gastrointestinal discomfort.
  • Local irritation at the infusion site.
  • Flushing or feeling of warmth.
  • Mild rash or pruritus.

Serious

  • Anaphylactic or severe allergic reactions, including urticaria and bronchospasm.
  • Volume overload leading to pulmonary edema or congestive heart failure.
  • Hemolysis or renal impairment in susceptible patients.
  • Transmission of infectious agents, although risk is extremely low with modern manufacturing.
  • Thromboembolic events due to increased viscosity.
  • Severe electrolyte disturbances such as hypernatremia.
  • Acute respiratory distress syndrome (ARDS) in rare cases.

Precautions & Warnings

Healthcare professionals should observe specific precautions when prescribing or administering Human Albumin CSL Behring to minimize risk and ensure appropriate use.

  • Assess fluid status and cardiac function before infusion to avoid overload.
  • Use caution in patients with renal impairment or severe liver disease.
  • Monitor vital signs and weight during and after administration.
  • Adjust dose in individuals with known hypersensitivity to albumin or plasma derivatives.
  • Avoid rapid infusion rates; administer over the recommended time frame.
  • Consider the risk of electrolyte imbalance, especially sodium, in patients on restrictive diets.
  • Document lot number and expiration date to trace product quality.

Avoid Interactions

Human Albumin CSL Behring may interact with other medications or solutions, requiring attention to compatibility and physiological effects.

Avoid

  • Co‑administration with other volume expanders that may cause fluid overload.
  • Simultaneous infusion of hypertonic saline solutions that could exacerbate hypernatremia.
  • Use with blood products containing incompatible preservatives.

Use with caution

  • Diuretics, as they may alter fluid balance and increase risk of hypovolemia.
  • Vasopressor agents, because changes in intravascular volume can affect hemodynamic response.
  • Anticoagulants, since rapid volume expansion may influence coagulation parameters.
  • Nephrotoxic drugs, given the potential for renal stress in volume‑overloaded states.

Frequently Asked Questions

It is primarily used to increase plasma oncotic pressure and restore intravascular volume in patients with hypovolemia, hypoalbuminemia, or during procedures that require volume expansion.

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

Use in patients with congestive heart failure requires careful monitoring of fluid status to avoid volume overload.

The manufacturing process includes viral inactivation steps, making the risk of infectious disease transmission extremely low, though not zero.

Vital signs, weight, and fluid balance should be monitored before, during, and after the infusion to detect any adverse reactions or overload.

Known hypersensitivity to human albumin or any component of the formulation is a contraindication.

Albumin exerts oncotic pressure, drawing fluid into the vascular space, whereas crystalloids distribute more evenly across compartments and do not significantly increase oncotic pressure.

Common side effects include mild fever, chills, transient blood pressure changes, headache, nausea, and local infusion site irritation.

Diuretics can be used, but clinicians should monitor fluid balance closely because combined effects may lead to hypovolemia.

The infusion rate should follow the prescribing information, typically administered slowly to reduce the risk of hypotension or other infusion‑related reactions.

Use in children should be based on clinical judgment and dosing guidelines specific to pediatric populations.

Store the solution at controlled room temperature, protect from light, and do not use after the expiration date indicated on the label.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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