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 electrolyte solution that combines calcium, magnesium, sodium, chloride, lactate, and hydrogen carbonate in a balanced formulation. It is supplied as a sterile liquid for infusion and is marketed in the European Union. The product is intended to support fluid and electrolyte balance in clinical settings where patients require intravenous replacement of essential minerals and buffering capacity.

Manufacturer / TM Owner

Vantive Belgium

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Indications & Clinical Uses

Hemosol B0 is used in hospital and clinical environments to address specific electrolyte and fluid needs. It is typically considered when patients have conditions that affect mineral balance or acid‑base status.

  • Replacement of calcium, magnesium, sodium, and chloride in patients with deficits.
  • Management of metabolic acidosis through lactate conversion to bicarbonate.
  • Support during major surgery or trauma when large fluid shifts occur.
  • Adjunct therapy for patients receiving parenteral nutrition.
  • Treatment of hypovolemia when isotonic fluid replacement is required.

Side Effects

Side effects of Hemosol B0 may vary in frequency and severity. Monitoring is recommended during administration.

Common

  • Mild hypercalcemia presenting as nausea or fatigue.
  • Transient hypermagnesemia causing flushing or warmth.
  • Slight elevation of serum sodium leading to mild thirst.
  • Temporary increase in urinary output.
  • Mild metabolic alkalosis reflected in blood gas analysis.

Serious

  • Severe hypercalcemia with cardiac arrhythmia.
  • Marked hypermagnesemia resulting in respiratory depression.
  • Rapid shifts in serum electrolytes causing seizures.
  • Overcorrection of acidosis leading to metabolic alkalosis complications.

Precautions & Warnings

When using Hemosol B0, clinicians should observe several safety considerations to minimize risk. Patient assessment and laboratory monitoring are essential.

  • Verify baseline electrolyte levels and acid‑base status before infusion.
  • Adjust infusion rate in patients with renal impairment to avoid accumulation.
  • Use caution in individuals with congestive heart failure or fluid overload risk.
  • Monitor cardiac rhythm in patients with known arrhythmias.
  • Avoid rapid bolus administration; prefer controlled infusion.
  • Ensure compatibility with other intravenous solutions before mixing.

Avoid Interactions

Hemosol B0 can interact with other medications or solutions, influencing electrolyte balance or infusion compatibility. Awareness of these interactions helps maintain patient safety.

Avoid

  • Co‑administration with calcium channel blockers that may exacerbate hypercalcemia.
  • Simultaneous infusion with high‑potassium solutions that could cause precipitation.
  • Use with certain blood products that may alter calcium levels.

Use with caution

  • Concurrent diuretics that affect sodium and magnesium excretion.
  • ACE inhibitors or ARBs in patients prone to hyperkalemia.
  • Antacids containing magnesium or aluminum.
  • Medications that influence renal handling of electrolytes, such as aminoglycosides.

Frequently Asked Questions

Hemosel B0 is used to replace lost electrolytes and provide buffering capacity in patients who require intravenous fluid therapy, helping maintain normal mineral balance and acid‑base status.

The solution contains calcium, magnesium, sodium, chloride, lactate (as a source of bicarbonate), and hydrogen carbonate.

Yes, but the infusion rate should be adjusted and electrolyte levels monitored closely because reduced renal function can affect clearance of calcium and magnesium.

Lactate is metabolized by the liver to bicarbonate, which helps correct metabolic acidosis by increasing the buffering capacity of the blood.

Regular checks of serum calcium, magnesium, sodium, chloride, and blood gas analysis are recommended, along with observation of cardiac rhythm and fluid status.

Compatibility should be confirmed for each medication; some solutions, especially those high in potassium or certain blood products, may be incompatible.

Common side effects include mild hypercalcemia, transient hypermagnesemia, slight increases in serum sodium, increased urine output, and mild metabolic alkalosis.

It should be avoided in patients with severe hypercalcemia, uncontrolled cardiac arrhythmias, or when co‑administered with incompatible IV solutions.

Unlike plain saline, Hemosol B0 provides a broader electrolyte profile and includes lactate/bicarbonate for buffering, making it suitable for more complex electrolyte disturbances.

The product should be stored at controlled room temperature, protected from light, and used before the expiration date indicated on the packaging.

Use in children is possible under specialist supervision, with dosing and infusion rates adjusted for age and weight, and with careful electrolyte monitoring.

Hemosol B0 is authorized as a medicinal product for intravenous use within the European Union and complies with EU pharmacovigilance regulations.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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