Product image of Haemaccel (Polygeline) supplied by GNH India

Haemaccel

Active Ingredient:
Polygeline
Origin:
EU

Haemaccel (Polygeline)

Haemaccel is a prescription‑only solution for injection that contains the colloid polygeline as its active ingredient. The product is supplied in an unspecified strength and is formulated as an intravenous fluid used to expand plasma volume. As a colloid plasma volume expander, Haemaccel works by increasing oncotic pressure within the bloodstream, helping to restore circulating volume in patients with fluid loss and supporting hemodynamic stability.

Manufacturer / TM Owner

Piramal Critical Care Limited

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Indications & Clinical Uses

Haemaccel is indicated for clinical situations where rapid plasma volume expansion is required.

  • Treatment of hypovolemia due to acute blood loss or dehydration.
  • Management of circulatory shock when immediate volume support is needed.
  • Intra‑operative fluid replacement to maintain adequate intravascular volume.
  • Adjunct therapy during major surgery to prevent hypotension.
  • Support for patients undergoing dialysis who require plasma expansion.
  • Use in trauma care to stabilize patients before definitive hemorrhage control.

Side Effects

The safety profile of Haemaccel includes a range of observed adverse reactions, which are generally categorized by frequency and severity.

Common

  • Mild, transient fever or chills occurring shortly after infusion.
  • Temporary elevation of blood pressure that resolves without intervention.
  • Local irritation or pain at the intravenous infusion site.
  • Nausea or mild gastrointestinal discomfort during or after administration.
  • Headache or dizziness that subsides within a few hours.

Serious

  • Anaphylactic or severe allergic reactions, including rash, bronchospasm, or hypotension.
  • Pulmonary edema resulting from fluid overload, especially in patients with cardiac dysfunction.
  • Renal impairment or decreased kidney function in susceptible individuals.

Precautions & Warnings

When using Haemaccel, clinicians should consider several precautionary measures to minimize risks and ensure appropriate patient selection.

  • Assess cardiac and renal function before administration, as fluid overload may exacerbate heart failure or kidney disease.
  • Avoid rapid infusion rates; follow recommended administration guidelines to reduce the chance of pulmonary edema.
  • Use caution in patients with known hypersensitivity to polygeline or other gelatin-derived products.
  • Monitor vital signs and fluid balance closely during and after infusion.
  • Do not administer concomitantly with large volumes of crystalloid solutions without adjusting total fluid input.

Avoid Interactions

Haemaccel may interact with other medications or clinical conditions; awareness of these interactions helps guide safe use.

Avoid

  • Avoid concurrent use with other colloid volume expanders, as combined oncotic load can increase risk of fluid overload.
  • Do not give with medications known to cause severe allergic reactions in gelatin-sensitive patients.

Use with caution

  • Use cautiously with diuretics, which may alter fluid balance and require adjustment of infusion volume.
  • Co‑administration with anticoagulants may enhance bleeding risk due to dilutional effects; monitor coagulation parameters.
  • Caution is advised when combined with drugs that affect renal function, such as aminoglycosides or NSAIDs, to prevent further kidney impairment.

Frequently Asked Questions

Haemaccel contains polygeline, a gelatin‑derived colloid that raises plasma oncotic pressure, thereby expanding the intravascular volume and helping to restore circulating blood volume.

Haemaccel is used for rapid plasma volume expansion in conditions such as hypovolemia, circulatory shock, intra‑operative fluid replacement, trauma stabilization, and as an adjunct during dialysis.

Haemaccel is supplied as a sterile solution for injection and is administered intravenously, usually through a controlled infusion pump to regulate the rate of delivery.

Caution is advised; patients with compromised cardiac function should be closely monitored for signs of fluid overload, and infusion rates may need to be reduced.

Common adverse reactions include mild fever or chills, transient increases in blood pressure, local infusion‑site irritation, nausea, headache, and dizziness.

Serious reactions include anaphylaxis, pulmonary edema, and renal impairment. If any of these occur, the infusion should be stopped and appropriate emergency care provided.

Yes. Patients with a documented hypersensitivity to polygeline, gelatin, or related compounds should not receive Haemaccel due to the risk of severe allergic reactions.

Because Haemaccel can dilute clotting factors, it may increase bleeding risk when used with anticoagulants. Monitoring of coagulation parameters is recommended.

Combination with diuretics should be done cautiously, as diuretics alter fluid balance. Dose adjustments and close monitoring of urine output and electrolytes are advisable.

Vital signs, central venous pressure, urine output, and overall fluid balance should be monitored regularly to detect early signs of overload or adverse reactions.

Haemaccel is primarily studied in adult populations; use in children should follow specific pediatric dosing guidelines and be supervised by a specialist.

The infusion should be stopped immediately, and emergency treatment with antihistamines, corticosteroids, or epinephrine should be administered according to standard anaphylaxis protocols.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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