Product image of Haemaccel (Polygeline) supplied by GNH India

Haemaccel

Active Ingredient:
Polygeline
Origin:
EU

Haemaccel (Polygeline)

Haemaccel is a solution for injection containing the colloid polygeline as the active ingredient. It is supplied in an unspecified strength as an intravenous fluid intended for volume expansion. The product is manufactured for the European market and is available by prescription only. Haemaccel works by providing oncotic pressure to increase intravascular plasma volume. It is used in settings to manage hypovolemia, shock, and fluid replacement during surgery or trauma.

Manufacturer / TM Owner

Piramal Critical Care B.V.

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Indications & Clinical Uses

Haemaccel is indicated for situations where rapid expansion of circulating blood volume is required.

  • Treatment of hypovolemia due to blood loss, dehydration, or burns.
  • Management of circulatory shock in trauma or postoperative patients.
  • Fluid replacement during major surgery when blood loss is anticipated.
  • Support of intravascular volume in patients with sepsis or severe infection.
  • Adjunctive therapy for electrolyte-free volume expansion in pediatric or adult patients.
  • Temporary plasma volume expansion in patients awaiting definitive blood transfusion.

Side Effects

Adverse reactions to Haemaccel are generally related to its colloid nature and the intravenous route of administration. These events are typically mild and resolve without specific treatment, but clinicians monitor patients closely for any signs of worsening.

Common

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

Serious

  • Anaphylactic or severe allergic reactions
  • Pulmonary edema due to fluid overload
  • Acute kidney injury in susceptible patients
  • Coagulopathy
  • Electrolyte imbalance

Precautions & Warnings

When using Haemaccel, clinicians should assess patient risk factors and monitor clinical parameters to minimize potential complications.

  • Evaluate cardiac function before infusion in patients with heart failure.
  • Use caution in individuals with renal impairment or reduced urine output.
  • Avoid rapid large-volume administration in patients at risk of pulmonary edema.
  • Monitor blood pressure and central venous pressure during and after infusion.
  • Check for signs of allergic reaction, especially in patients with known colloid sensitivities.
  • Adjust dosage in pediatric patients based on weight and clinical response.
  • Discontinue infusion if severe hypotension or anaphylaxis occurs.

Avoid Interactions

Haemaccel may interact with other intravenously administered agents, influencing fluid balance, coagulation, or cardiovascular stability.

Avoid

  • Concurrent infusion of other synthetic colloids (e.g., hydroxyethyl starch) due to additive risk of renal dysfunction.
  • Simultaneous administration of high-dose vasopressors without volume assessment, which can exacerbate hypertension.

Use with caution

  • Blood products such as packed red cells, as volume status should be balanced.
  • Diuretics, because they may alter the intended plasma expansion effect.
  • ACE inhibitors or ARBs, which can affect blood pressure response to volume loading.
  • Anticoagulants, since rapid plasma expansion may influence coagulation parameters.

Frequently Asked Questions

Haemaccel is a sterile solution for injection that contains the colloid polygeline. It works by creating oncotic pressure in the bloodstream, which draws fluid into the vascular compartment and expands plasma volume.

Haemaccel is commonly used for hypovolemia, circulatory shock, and fluid replacement during surgery, trauma, or severe infection when rapid plasma volume expansion is needed.

Haemaccel is administered intravenously, usually as an infusion. The rate and total volume are determined by the patient’s clinical condition and response to therapy.

Common adverse effects include mild fever, chills, transient changes in blood pressure, nausea, vomiting, headache, dizziness, and local irritation at the injection site.

Serious reactions may include anaphylaxis, pulmonary edema from fluid overload, acute kidney injury, coagulopathy, and significant electrolyte disturbances.

Patients with known hypersensitivity to polygeline or other gelatin-based products, and those with uncontrolled heart failure or severe renal impairment, should avoid Haemaccel.

Clinicians should monitor blood pressure, central venous pressure, urine output, and signs of allergic reaction throughout the infusion and for a period afterward.

Haemaccel can be administered alongside blood products, but the overall fluid balance should be carefully assessed to avoid volume overload.

Diuretics may reduce the plasma‑expanding effect of Haemaccel; therefore, dosage adjustments and close monitoring of fluid status are recommended.

Haemaccel may be used in children when weight‑based dosing is applied and the patient is closely monitored for hemodynamic changes.

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

Unlike crystalloids, Haemaccel is a colloid that remains in the vascular space longer, providing a greater and more sustained increase in plasma oncotic pressure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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