GNH USA

Europe — EMA

Hemosol B0

Learn about Hemosol B0 intravenous electrolyte solution, its uses, side effects, precautions, and drug interactions for clinical fluid management.

Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate

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What is 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.

What is Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate used for?

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.

What are the side effects of Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate?

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.

What precautions apply to Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate?

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.

What does Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate interact with?

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

What is the primary purpose of Hemosol B0 in clinical practice?+
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.
Which electrolytes are included in the composition of Hemosol B0?+
The solution contains calcium, magnesium, sodium, chloride, lactate (as a source of bicarbonate), and hydrogen carbonate.
Can Hemosol B0 be used for patients with renal impairment?+
Yes, but the infusion rate should be adjusted and electrolyte levels monitored closely because reduced renal function can affect clearance of calcium and magnesium.
How does lactate in Hemosol B0 contribute to acid‑base regulation?+
Lactate is metabolized by the liver to bicarbonate, which helps correct metabolic acidosis by increasing the buffering capacity of the blood.
What monitoring is recommended during Hemosol B0 administration?+
Regular checks of serum calcium, magnesium, sodium, chloride, and blood gas analysis are recommended, along with observation of cardiac rhythm and fluid status.
Is Hemosol B0 compatible with other intravenous medications?+
Compatibility should be confirmed for each medication; some solutions, especially those high in potassium or certain blood products, may be incompatible.
What are common side effects patients might experience with Hemosol B0?+
Common side effects include mild hypercalcemia, transient hypermagnesemia, slight increases in serum sodium, increased urine output, and mild metabolic alkalosis.
When should Hemosol B0 be avoided in a patient?+
It should be avoided in patients with severe hypercalcemia, uncontrolled cardiac arrhythmias, or when co‑administered with incompatible IV solutions.
How does Hemosol B0 differ from standard saline 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.
What are the storage requirements for Hemosol B0?+
The product should be stored at controlled room temperature, protected from light, and used before the expiration date indicated on the packaging.
Can Hemosol B0 be used in pediatric patients?+
Use in children is possible under specialist supervision, with dosing and infusion rates adjusted for age and weight, and with careful electrolyte monitoring.
What is the regulatory status of Hemosol B0 in the EU?+
Hemosol B0 is authorized as a medicinal product for intravenous use within the European Union and complies with EU pharmacovigilance regulations.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Calcium, Lactic Acid, Magnesium, Sodium, Chloride Ion, Hydrogen Carbonate
Route
Haemodialysis , Intravenous Use
Manufacturer
Vantive Belgium
Origin
EU

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