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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 containing calcium, lactic acid, magnesium, sodium, chloride ion, and hydrogen carbonate. It is formulated for use in haemodialysis and other intravenous applications, providing electrolyte and acid‑base balance support. The product is marketed in the European Union and supplied without a specific brand name, adhering to standard pharmaceutical quality specifications. The solution is sterile, isotonic, and intended for administration under medical supervision.

Manufacturer / TM Owner

Vantive Belgium

1
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Indications & Clinical Uses

Hemosol B0 is primarily employed in clinical settings where precise electrolyte and acid‑base management is required.

  • Maintenance of electrolyte concentrations during haemodialysis.
  • Correction of mild metabolic acidosis in patients receiving renal replacement therapy.
  • Support of calcium and magnesium balance in critically ill patients.
  • Provision of sodium and chloride to stabilize plasma osmolality.
  • Use as a compatible carrier solution for intravenous drug admixtures.

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 vomiting.
  • Slight increase in serum calcium or magnesium levels.
  • Temporary headache or dizziness.

Serious

  • Severe hypercalcemia or hypermagnesemia.
  • Rapid shifts in blood pH leading to metabolic alkalosis.
  • Anaphylactic or severe hypersensitivity reactions.
  • Pulmonary edema from fluid overload.

Precautions & Warnings

When using Hemosol B0, clinicians should observe several precautionary measures to minimize risk.

  • Verify patient electrolyte and acid‑base status before initiation.
  • Adjust infusion rate in patients with cardiac or renal impairment.
  • Monitor serum calcium, magnesium, and bicarbonate levels during therapy.
  • Avoid use in patients with known hypersensitivity to any component.
  • Use caution in pregnant or lactating individuals until safety is established.
  • Ensure compatibility with other intravenous solutions to prevent precipitation.

Avoid Interactions

Hemosol B0 may interact with other medications or solutions; awareness of these interactions helps maintain safety.

Avoid

  • Concurrent administration with calcium channel blockers that may exacerbate hypercalcemia.
  • Co‑infusion with high‑dose bicarbonate solutions, which can cause excessive alkalosis.
  • Use with blood products containing citrate, increasing risk of electrolyte imbalance.

Use with caution

  • Loop diuretics, which can alter calcium and magnesium excretion.
  • ACE inhibitors or ARBs, where shifts in sodium and potassium may affect blood pressure control.
  • Anticoagulants used during haemodialysis, requiring monitoring of clotting parameters.

Frequently Asked Questions

Hemosol B0 is used to maintain electrolyte balance and support acid‑base homeostasis during haemodialysis treatments.

The solution provides calcium, magnesium, sodium, chloride, and bicarbonate (as hydrogen carbonate) along with lactic acid.

Yes, it is compatible with many IV drugs, but compatibility should be confirmed before admixture.

Regular checks of serum calcium, magnesium, sodium, chloride, and bicarbonate levels are advised, as well as observation for infusion site reactions.

Infusion rates may need adjustment in patients with cardiac impairment, and fluid status should be closely monitored.

Common effects include mild infusion site irritation, transient nausea, slight electrolyte shifts, headache, or dizziness.

Serious reactions may involve hypercalcemia, hypermagnesemia, metabolic alkalosis, severe hypersensitivity, or fluid overload leading to pulmonary edema.

Yes, it should not be used in individuals with documented hypersensitivity to any of its components.

Concurrent use may increase the risk of hypercalcemia, so clinicians should avoid combining them when possible.

Use in pregnancy should be approached with caution, and the benefits must be weighed against potential risks.

The European Medicines Agency (EMA) is responsible for the regulatory oversight of Hemosol B0 within the European Union.

It may be employed in CRRT to provide electrolyte and acid‑base support, but dosing and compatibility should be evaluated by the treating team.

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GNH India Pharmaceuticals Limited

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