Product image of Hemosol B0 (Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate) supplied by GNH India

Hemosol B0

Active Ingredient:
Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate
Origin:
EU

Hemosol B0 (Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate)

Hemosol B0 is a sterile dialysis solution formulated with calcium, lactic acid, magnesium, sodium, chloride ion, and hydrogen carbonate. It is supplied as a solution for injection intended for use in hemodialysis circuits. The product is manufactured for the European market and is classified as a renal replacement therapy solution that helps maintain electrolyte and acid‑base balance during extracorporeal blood treatment and overall patient safety.

Manufacturer / TM Owner

Vantive Belgium

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Indications & Clinical Uses

Hemosol B0 is indicated for use in clinical settings where hemodialysis or other forms of renal replacement therapy are required.

  • Provides electrolyte replacement during standard hemodialysis sessions.
  • Supports acid‑base regulation in patients with chronic kidney disease undergoing dialysis.
  • Can be used as a dialysate component in continuous renal replacement therapy (CRRT).
  • Suitable for use in both adult and pediatric dialysis protocols when appropriate concentration adjustments are made.
  • Facilitates maintenance of calcium and magnesium balance during high‑flux dialysis procedures.

Side Effects

Adverse events associated with Hemosol B0 are generally related to its electrolyte composition and are reported in clinical practice.

Common

  • Mild transient hypotension during dialysis, often self‑limiting and managed by adjusting ultrafiltration.
  • Slight rise in serum calcium or magnesium that usually normalizes without additional therapy.
  • Minor discomfort at the vascular access site, alleviated by standard catheter care.

Serious

  • Severe hypercalcemia that may cause cardiac arrhythmia and requires prompt medical intervention.
  • Acute metabolic alkalosis from excess buffering agents, possibly needing dialysate composition adjustment.
  • Anaphylactic or severe hypersensitivity reaction to solution components, demanding immediate emergency treatment.

Precautions & Warnings

When using Hemosol B0, clinicians should observe specific precautions to ensure patient safety and optimal dialysis performance.

  • Verify patient electrolyte baseline values before initiating treatment to avoid over‑correction.
  • Adjust calcium and magnesium concentrations for patients with known cardiac or neuromuscular disorders.
  • Monitor acid‑base status regularly during therapy, especially in patients prone to metabolic alkalosis.
  • Use compatible infusion sets and tubing to prevent precipitation of calcium salts.
  • Ensure proper storage conditions (controlled temperature, protection from light) to maintain solution stability.

Avoid Interactions

Hemosol B0 may interact with certain medications or clinical conditions; awareness of these interactions helps prevent complications during dialysis.

Avoid

  • Concurrent administration of calcium‑containing intravenous drugs that could cause hypercalcemia.
  • Use with high‑dose bicarbonate or other strong alkalinizing agents that may exacerbate metabolic alkalosis.

Use with caution

  • Loop diuretics, which can alter sodium and chloride balance during treatment.
  • Beta‑blockers, as they may mask signs of hypotension related to dialysis.
  • Anticoagulants (e.g., heparin) requiring close monitoring of clotting parameters.

Frequently Asked Questions

Hemosol B0 includes calcium, magnesium, sodium, chloride ion, hydrogen carbonate, and lactic acid as a buffering agent.

The solution can be used in adult and pediatric dialysis protocols when appropriate concentration adjustments are made under clinical supervision.

Hydrogen carbonate and lactic acid in the formulation act as buffering agents that help regulate pH levels in the blood during extracorporeal treatment.

Yes, Hemosol B0 is suitable as a dialysate component for CRRT when the prescribed settings match the patient’s electrolyte needs.

Regular checks of serum calcium, magnesium, sodium, chloride, and bicarbonate levels, as well as blood pressure and acid‑base status, are advised.

Hemosol B0 should be avoided in patients with known hypersensitivity to any of its components or in cases where extreme electrolyte imbalances are present without correction.

The dialysis prescription should be reviewed, calcium concentration may be reduced, and appropriate medical management should be initiated promptly.

The regulatory status of Hemosol B0 varies by jurisdiction; it is typically supplied under prescription or medical supervision for dialysis use.

Store the solution at the temperature recommended by the manufacturer, protect it from direct light, and keep the container sealed until use.

Mixing with other solutions is not recommended unless specifically directed by a healthcare professional, as incompatibilities may lead to precipitation.

Serious reactions may include severe hypercalcemia symptoms, metabolic alkalosis, or anaphylaxis, which require immediate medical attention.

The formulation is a sterile solution for injection and typically does not contain additional preservatives, but the exact composition should be confirmed from the product label.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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