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Human Albumin Baxalta

Active Ingredient:
Human Serum Albumin
Origin:
EU

Human Albumin Baxalta (Human Serum Albumin)

Human Albumin Baxalta is a sterile solution for injection that contains human serum albumin as the active ingredient. Provided as an intravenous albumin solution, it is manufactured for the European market and classified as a plasma protein used as a volume expander. The product is prescription‑only and is used when rapid restoration of circulatory volume or correction of low serum albumin is needed clinically.

Manufacturer / TM Owner

Baxalta Innovations Gmbh

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Indications & Clinical Uses

Human Albumin Baxalta is employed in clinical settings where plasma volume expansion or albumin replacement is required.

  • Treatment of hypovolemia associated with acute blood loss or dehydration.
  • Management of shock, including septic or hemorrhagic shock.
  • Support for patients with extensive burns to maintain intravascular volume.
  • Correction of hypoalbuminemia in liver disease, nephrotic syndrome, or chronic malnutrition.
  • Adjunct therapy during renal dialysis when low albumin contributes to fluid shifts.
  • Perioperative volume management in major surgery.

How It Works

  • Human Albumin Baxalta works by increasing the oncotic pressure of plasma. The infused human serum albumin molecules bind water within the vascular compartment, drawing fluid from the interstitial space back into the bloodstream. This rise in oncotic pressure expands intravascular volume, improves tissue perfusion, and helps maintain hemodynamic stability. The albumin also serves as a carrier for endogenous substances such as hormones, fatty acids, and drugs.

Side Effects

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

Common

  • Transient fever or chills.
  • Mild hypotension or hypertension.
  • Headache.
  • Nausea or vomiting.
  • Local irritation at the infusion site.

Serious

  • Anaphylactic or severe allergic reactions.
  • Acute hemolysis.
  • Volume overload leading to pulmonary edema.
  • Thromboembolic events.
  • Renal dysfunction.

Precautions & Warnings

Clinicians should evaluate patient history and clinical status before administering Human Albumin Baxalta to minimize risk.

  • Assess for known hypersensitivity to human albumin or any component of the solution.
  • Use caution in patients with congestive heart failure or pulmonary edema due to risk of volume overload.
  • Monitor fluid balance and electrolytes during and after infusion.
  • Avoid rapid infusion rates that may provoke cardiovascular instability.
  • Evaluate renal and hepatic function, as impairment may affect albumin metabolism.
  • Consider the potential for increased intracranial pressure in patients with head trauma.

Avoid Interactions

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

Avoid

  • Concurrent administration of other volume expanders (e.g., synthetic colloids) without careful monitoring.
  • Use with drugs that have a high risk of anaphylaxis, such as certain antibiotics or contrast agents, without pre‑medication.

Use with caution

  • Diuretics, which may exacerbate intravascular volume shifts.
  • Vasopressors, as combined effects on blood pressure require close observation.
  • Anticoagulants, because changes in plasma protein levels can alter drug binding.
  • Immunosuppressants, due to potential modulation of immune reactions.

Frequently Asked Questions

Human Albumin Baxalta is used as a plasma volume expander to restore intravascular volume and to correct low serum albumin levels in various medical conditions.

The product is administered intravenously as a sterile solution for injection.

It can be used with caution; clinicians should monitor for signs of volume overload because patients with congestive heart failure are at higher risk.

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

The albumin solution may be employed in the management of hypovolemic, septic, or hemorrhagic shock when rapid plasma volume expansion is needed.

Infused albumin increases plasma oncotic pressure, which draws fluid from the interstitial space into the vascular compartment, expanding circulating blood volume.

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

The solution should be stored according to the manufacturer’s instructions, typically refrigerated and protected from light until the expiration date.

Common reactions include transient fever or chills, mild changes in blood pressure, headache, nausea, vomiting, and local infusion site irritation.

Concurrent use with other volume expanders should be avoided or closely monitored to prevent excessive fluid accumulation.

Yes, it may be used as an adjunct in renal dialysis when low albumin contributes to fluid shifts and volume management is required.

Patients with severe burns, liver disease, nephrotic syndrome, major surgery, or any condition causing hypoalbuminemia or significant fluid loss may benefit.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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