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 solution that contains calcium, magnesium, sodium, chloride, hydrogen carbonate and lactic acid. It is supplied as a sterile liquid for use in haemodialysis and other intravenous applications. The product is marketed in the European Union and is available only by prescription. It is designed to help maintain electrolyte balance and acid‑base status during renal replacement therapy.

Manufacturer / TM Owner

Vantive Belgium

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Indications & Clinical Uses

Hemosol B0 is used in clinical settings where precise control of electrolytes and acid‑base balance is required, especially during renal replacement procedures. It may be employed for the following purposes:

  • Replacement of calcium, magnesium and sodium losses during haemodialysis.
  • Correction of metabolic acidosis in patients receiving dialysis.
  • Maintenance of plasma volume and osmotic balance in critically ill patients.
  • Support of cardiac and neuromuscular function when electrolyte disturbances are present.
  • Adjunct therapy for patients with chronic kidney disease undergoing intermittent dialysis.

Side Effects

Side effects of Hemosol B0 are generally related to its electrolyte composition and the rate of infusion. They are reported in clinical practice and may vary in frequency and severity.

Common

  • Mild nausea or vomiting.
  • Transient hypotension or dizziness during rapid infusion.
  • Mild headache.
  • Local irritation at the infusion site.
  • Temporary changes in serum calcium or magnesium levels.

Serious

  • Hypercalcemia leading to cardiac arrhythmias.
  • Severe metabolic alkalosis.
  • Pulmonary edema from excessive volume load.
  • Acute coronary syndrome in patients with underlying heart disease.
  • Severe electrolyte imbalance requiring urgent medical intervention.

Precautions & Warnings

When prescribing or administering Hemosol B0, clinicians should observe several safety considerations to minimize risk.

  • Monitor serum calcium, magnesium, sodium and bicarbonate levels before, during, and after infusion.
  • Avoid use in patients with known hypercalcemia or severe metabolic alkalosis.
  • Adjust infusion rate in patients with compromised cardiac function or fluid overload risk.
  • Use caution in individuals receiving other electrolyte-containing solutions to prevent cumulative excess.
  • Ensure compatibility with other intravenous medications; incompatibility may cause precipitation.
  • Store the solution according to manufacturer guidelines to maintain sterility and potency.

Avoid Interactions

Hemosol B0 may interact with other medications or solutions administered intravenously. Awareness of potential interactions helps maintain patient safety.

Avoid

  • Simultaneous infusion of calcium‑containing solutions with phosphate binders, which can precipitate calcium phosphate.
  • Co‑administration with high‑dose potassium supplements, as electrolyte shifts may become unpredictable.

Use with caution

  • Loop diuretics, which can amplify calcium and magnesium losses.
  • ACE inhibitors or ARBs, which may affect renal handling of electrolytes.
  • Beta‑blockers, especially in patients prone to bradycardia when calcium levels rise.
  • Anticoagulants used during dialysis, as electrolyte shifts can influence coagulation parameters.

Frequently Asked Questions

Hemosol B0 contains calcium, magnesium, sodium, chloride ion, hydrogen carbonate (bicarbonate) and lactic acid in a sterile aqueous solution.

It is primarily used during haemodialysis to help maintain electrolyte and acid‑base balance.

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

The solution should be stored at controlled room temperature, protected from light, and kept in its original sealed container until administration.

Compatibility should be confirmed with the pharmacy; generally it can be co‑administered with compatible crystalloids but may precipitate with phosphate‑containing solutions.

Regular monitoring of serum calcium, magnesium, sodium, bicarbonate, and overall fluid balance is recommended throughout the infusion.

Common side effects include mild nausea, transient hypotension, headache, local infusion site irritation, and temporary changes in electrolyte levels.

It should be avoided in patients with documented hypercalcemia, severe metabolic alkalosis, or known incompatibility with other infused solutions.

Yes, loop diuretics, ACE inhibitors/ARBs, beta‑blockers, and high‑dose potassium supplements should be used with caution due to potential electrolyte interactions.

The infusion should be stopped immediately, the patient should receive appropriate medical care, and the event should be reported to the prescribing physician and pharmacovigilance authorities.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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