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 electrolyte solution containing calcium, magnesium, sodium, chloride, and bicarbonate, provided as a sterile solution for intravenous infusion. It is used primarily in renal replacement therapy to support haemodialysis procedures and to correct electrolyte and acid‑base disturbances. The product is manufactured for the European market and is available by prescription only.

Manufacturer / TM Owner

Vantive Belgium

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Indications & Clinical Uses

Hemosol B0 is indicated for use in clinical settings where precise electrolyte management is required. It is commonly employed during renal replacement therapies and for correcting imbalances in patients receiving haemodialysis.

  • Provides essential calcium, magnesium, sodium, and chloride during haemodialysis sessions.
  • Supplies bicarbonate to help maintain acid‑base balance.
  • Supports intravenous fluid therapy when electrolyte replacement is needed.
  • Assists in the management of metabolic acidosis in acute care.
  • Used as a component of dialysis fluid formulations.
  • May be administered in conjunction with other renal support solutions under medical supervision.

Side Effects

Side effects of Hemosol B0 are generally related to its electrolyte composition and the route of administration. Most adverse reactions are mild and transient, but serious events can occur in susceptible individuals.

Common

  • Mild infusion site irritation or erythema.
  • Transient nausea or vomiting.
  • Temporary headache.
  • Mild electrolyte shifts such as hypercalcemia or hypermagnesemia.
  • Slight increase in blood pressure during rapid infusion.

Serious

  • Severe hyperkalemia or hypocalcemia if dosing errors occur.
  • Acute pulmonary edema from fluid overload.
  • Anaphylactic or severe hypersensitivity reactions.
  • Cardiac arrhythmias related to electrolyte imbalance.
  • Metabolic alkalosis from excessive bicarbonate administration.

Precautions & Warnings

When using Hemosol B0, clinicians should consider patient-specific factors and monitor relevant parameters closely. The solution should be administered according to established protocols.

  • Verify electrolyte levels before and during infusion.
  • Adjust infusion rate in patients with compromised cardiac function.
  • Use caution in individuals with fluid overload or congestive heart failure.\n- Monitor acid‑base status to avoid metabolic alkalosis.
  • Ensure compatibility with other intravenous solutions.
  • Store according to manufacturer guidelines to maintain sterility.
  • Discontinue use and seek medical advice if signs of hypersensitivity appear.

Avoid Interactions

Hemosol B0 may interact with other medications or solutions that affect electrolyte balance or acid‑base status. Awareness of potential interactions helps prevent complications.

Avoid

  • Concurrent administration of high‑dose calcium or magnesium supplements without monitoring.
  • Use with potassium‑rich solutions in patients at risk of hyperkalemia.
  • Simultaneous infusion of acidic drugs that could counteract bicarbonate buffering.

Use with caution

  • Loop diuretics that may exacerbate electrolyte loss.
  • ACE inhibitors or ARBs that influence potassium levels.
  • Sodium‑containing medications that could contribute to fluid overload.
  • Blood transfusions that may affect calcium and magnesium concentrations.

Frequently Asked Questions

Hemosol B0 provides essential electrolytes and a bicarbonate buffer to maintain electrolyte balance and correct acid‑base disturbances during haemodialysis.

It can be used with caution; clinicians should monitor fluid status and adjust infusion rates to avoid fluid overload in heart failure patients.

The solution contains calcium, magnesium, sodium, chloride, and bicarbonate as the primary electrolyte components.

Use in pediatric patients should follow specific medical guidance and dosing adjustments; it is not automatically approved for children without physician oversight.

Store the solution at controlled room temperature, protected from light, and keep the container sealed until administration to maintain sterility.

Regular monitoring of serum electrolytes, blood pressure, and acid‑base status is recommended throughout the infusion.

Compatibility should be confirmed; avoid mixing with solutions that contain high potassium or acidic agents that could alter the intended electrolyte balance.

Serious reactions may include severe electrolyte imbalance, pulmonary edema, cardiac arrhythmias, or anaphylactic symptoms such as difficulty breathing and rash.

Yes, Hemosol B0 is a prescription‑only medication and must be ordered by a qualified healthcare professional.

The bicarbonate component acts as a buffer, raising blood pH and helping to neutralize excess acidity during renal replacement therapy.

The infusion should be paused, the site evaluated, and the healthcare provider consulted to determine whether to continue, adjust the rate, or discontinue the solution.

Contraindications include known hypersensitivity to any component of the solution and conditions where rapid electrolyte shifts could be harmful; clinical judgment is required.

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GNH India Pharmaceuticals Limited

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Last updated:

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