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 an intravenous dialysis solution containing calcium, lactic acid, magnesium, sodium, chloride ion, and hydrogen carbonate. It is supplied as a sterile solution for infusion during haemodialysis, providing electrolyte and bicarbonate buffering. The product is manufactured for the EU market and is prescribed for renal replacement therapy. It is intended for use under medical supervision and is classified as a prescription‑only electrolyte solution.

Manufacturer / TM Owner

Vantive Belgium

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Indications & Clinical Uses

Hemosol B0 is used as the dialysate fluid during haemodialysis procedures to support patients with end‑stage renal disease.

  • Provides calcium and magnesium to maintain plasma electrolyte levels during dialysis.
  • Supplies sodium and chloride to help regulate fluid balance.
  • Delivers hydrogen carbonate as a bicarbonate buffer to correct metabolic acidosis.
  • Supports overall acid‑base homeostasis throughout the treatment session.
  • Can be employed in continuous renal replacement therapy (CRRT) where compatible.

Side Effects

Adverse reactions to Hemosol B0 are generally uncommon, but patients may experience effects related to its electrolyte composition or buffering capacity.

Common

  • Mild transient hypotension during infusion.
  • Slight nausea or vomiting.
  • Mild pruritus at the infusion site.
  • Temporary changes in serum calcium or magnesium levels.

Serious

  • Severe hypercalcemia or hypermagnesemia.
  • Metabolic alkalosis from excessive bicarbonate.
  • Acute pulmonary edema due to fluid overload.
  • Anaphylactic or severe allergic reaction to the solution.

Precautions & Warnings

Clinicians should observe specific precautions when prescribing Hemosol B0 to ensure patient safety and optimal dialysis outcomes.

  • Verify patient’s baseline electrolyte and acid‑base status before initiating treatment.
  • Adjust dialysate composition for patients with known hypercalcemia, hypermagnesemia, or severe metabolic alkalosis.
  • Monitor blood pressure and fluid balance closely during the session.
  • Use only with compatible haemodialysis machines and tubing sets.
  • Avoid use in patients with known hypersensitivity to any component of the solution.
  • Document any adverse events and report according to local regulations.

Avoid Interactions

Hemosol B0 may interact with certain medications or clinical conditions, requiring careful management.

Avoid

  • Concurrent administration of calcium channel blockers that may potentiate hypercalcemia.
  • High-dose vitamin D analogues that increase calcium absorption.
  • Sodium‑containing medications that could exacerbate fluid overload.

Use with caution

  • Loop diuretics, as they may alter intravascular volume and electrolyte shifts.
  • ACE inhibitors or ARBs, which can affect potassium and blood pressure during dialysis.
  • Anticoagulants, because changes in calcium levels can influence coagulation pathways.

Frequently Asked Questions

Hemosol B0 contains calcium, lactic acid, magnesium, sodium, chloride ion, and hydrogen carbonate as its active electrolyte constituents.

The hydrogen carbonate (bicarbonate) in Hemosol B0 acts as a buffer, neutralizing excess acids in the blood and supporting normal pH during the dialysis session.

It is used in standard intermittent haemodialysis, as well as in continuous renal replacement therapy (CRRT) when compatible with the equipment.

Baseline and periodic checks of serum electrolytes, acid‑base status, blood pressure, and fluid balance are recommended throughout treatment.

Yes, Hemosol B0 can be employed in CRRT protocols provided the dialysis machine and tubing are compatible with the solution.

Common effects include mild hypotension, transient nausea or vomiting, mild itching at the infusion site, and temporary shifts in calcium or magnesium levels.

Management may involve adjusting the calcium concentration in the dialysate, reducing calcium‑containing medications, and closely monitoring serum calcium levels.

Hemosol B0 should not be used in patients with a known hypersensitivity to any of its components or in those with uncontrolled severe metabolic alkalosis.

Avoid high‑dose vitamin D analogues and calcium‑containing drugs that may raise calcium levels. Use loop diuretics, ACE inhibitors, ARBs, and anticoagulants with caution, monitoring electrolytes and fluid status.

Hemosol B0 provides a specific concentration of hydrogen carbonate designed to buffer metabolic acids effectively, which may differ from other solutions that use alternative buffering agents or concentrations.

Hemosol B0 is administered intravenously as part of the haemodialysis circuit, delivering the solution directly into the dialysate stream.

No, Hemosol B0 is a prescription‑only product and must be prescribed by a qualified healthcare professional.

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GNH India Pharmaceuticals Limited

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Last updated:

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