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 aqueous electrolyte solution that contains calcium, magnesium, sodium, chloride, bicarbonate and lactate. It is supplied in a ready‑to‑use liquid form for intravenous infusion or incorporation into haemodialysis circuits. The product is marketed in the European Union and is prescribed by healthcare professionals for electrolyte management during renal replacement therapy and related clinical situations.

Manufacturer / TM Owner

Vantive Belgium

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Indications & Clinical Uses

Hemosol B0 is indicated for clinical situations that require controlled electrolyte replacement and acid‑base balance. It is commonly employed in the following contexts:

  • Renal replacement therapy, specifically haemodialysis, to provide essential cations and anions.
  • Intravenous electrolyte supplementation in patients with acute or chronic electrolyte disturbances.
  • Maintenance of plasma osmolarity during prolonged infusion therapy.
  • Supportive care for patients undergoing major surgery or trauma with anticipated fluid shifts.
  • Adjunctive therapy in critical care settings where precise electrolyte control is required.

Side Effects

Adverse reactions to Hemosol B0 are generally infrequent, but they can be categorized by frequency and severity.

Common

  • Mild infusion site irritation or erythema.
  • Transient nausea or mild abdominal discomfort.
  • Slight increase in serum calcium or magnesium levels that resolves without intervention.
  • Temporary changes in blood pressure related to fluid volume shifts.

Serious

  • Hyperkalemia or severe electrolyte imbalance if administered in error.
  • Acute pulmonary edema from rapid volume overload.
  • Severe allergic reaction or anaphylaxis, though rare.
  • Metabolic alkalosis due to excess bicarbonate administration.
  • Cardiac arrhythmias associated with abrupt electrolyte changes.

Precautions & Warnings

When using Hemosol B0, clinicians should observe several safety considerations to minimise risk. Important precautions include:

  • Verify patient electrolyte status and acid‑base balance before initiation.
  • Adjust infusion rates in patients with compromised cardiac or pulmonary function.
  • Monitor serum calcium, magnesium, sodium, and bicarbonate levels regularly during therapy.
  • Use caution in individuals with known hypersensitivity to any component of the solution.
  • Ensure proper storage conditions to maintain solution sterility and stability.
  • Document any adverse events promptly and report according to local regulations.

Avoid Interactions

Hemosol B0 may interact with other medications or solutions administered concurrently. Awareness of these interactions helps prevent complications.

Avoid

  • Co‑administration with calcium channel blockers that may potentiate calcium overload.
  • Simultaneous infusion of high‑potassium solutions, which can exacerbate hyperkalemia.
  • Use with acidic drug formulations that could precipitate when mixed with bicarbonate.

Use with caution

  • Concurrent use of diuretics that alter sodium or magnesium balance.
  • Administration alongside other intravenous fluids containing overlapping electrolytes.
  • Patients receiving anticoagulants, as rapid volume shifts may affect hemodynamics.
  • Situations where rapid correction of acidosis is required, to avoid over‑correction.

Frequently Asked Questions

Hemosol B0 contains calcium, magnesium, sodium, chloride, bicarbonate (as hydrogen carbonate) and lactate, providing a balanced electrolyte composition for dialysis and intravenous use.

Yes, the solution is formulated for incorporation into haemodialysis circuits as well as for direct intravenous infusion when electrolyte replacement is needed.

Hemosol B0 is classified as a prescription‑only medication and must be ordered and administered under the supervision of a qualified healthcare professional.

The product should be stored at controlled room temperature, protected from light, and kept in its original sealed container to maintain sterility and chemical stability.

Clinicians should regularly monitor serum electrolytes, acid‑base status, blood pressure, and fluid balance throughout the infusion or dialysis session.

Hemosol B0 should be avoided in patients with known hypersensitivity to any of its components and used with caution in those with severe cardiac or pulmonary disease.

Mixing should be avoided unless compatibility has been confirmed, as some drugs may precipitate or alter the electrolyte balance when combined with the solution.

Lactate serves as a metabolizable buffer that helps maintain acid‑base equilibrium, particularly during haemodialysis where bicarbonate levels are critical.

Unlike simple saline, Hemosol B0 provides a broader spectrum of electrolytes and a bicarbonate buffer, making it suitable for precise electrolyte management in dialysis and critical care.

The solution is compatible with standard haemodialysis machines and can be connected to the dialysate circuit according to the manufacturer’s instructions.

The infusion should be stopped immediately, the patient evaluated, and appropriate medical treatment administered. The event should be documented and reported per local pharmacovigilance guidelines.

The safety of Hemosol B0 in pregnancy has not been established; it should only be used if the potential benefit justifies any potential risk to the fetus.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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