Product image of Hospasol (Sodium Hydrogen Carbonate) supplied by GNH India

Hospasol

Active Ingredient:
Sodium Hydrogen Carbonate
Origin:
EU

Hospasol (Sodium Hydrogen Carbonate)

Hospasol is an intravenous preparation containing sodium hydrogen carbonate as its sole active ingredient. The product is supplied in a sterile solution for parenteral administration, with the specific concentration not disclosed in the public label. Originating from the European Union market, Hospasol is classified as a pharmaceutical agent used to modify systemic acid‑base balance when rapid correction is required in clinical settings under medical supervision.

Manufacturer / TM Owner

Vantive B.V.

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Indications & Clinical Uses

Hospasol is employed in medical practice where rapid adjustment of blood pH is needed.

  • Correction of metabolic acidosis during surgery or critical care.
  • Management of severe electrolyte disturbances associated with acid‑base imbalance.
  • Adjunct in cardiopulmonary bypass circuits to maintain appropriate pH.
  • Supportive therapy for patients receiving large volumes of chloride‑rich fluids.
  • Use in renal replacement therapies to buffer systemic acidity.
  • Preparation of buffered solutions for laboratory or diagnostic use in hospital settings.

How It Works

  • Sodium hydrogen carbonate, when administered intravenously, dissociates into sodium (Na⁺) and bicarbonate (HCO₃⁻) ions. The bicarbonate acts as a systemic buffer, combining with excess hydrogen ions to form carbonic acid, which is rapidly converted to water and carbon dioxide for exhalation. This shift reduces plasma hydrogen ion concentration, thereby raising the arterial pH toward normal physiological levels. The sodium component contributes to extracellular fluid volume and electrolyte balance.

Side Effects

Adverse reactions to intravenous sodium hydrogen carbonate are generally related to its alkalinizing effect and electrolyte load.

Common

  • Transient facial flushing or a sensation of warmth during the infusion.
  • Mild nausea, occasional vomiting, or abdominal discomfort.
  • Temporary rise in serum sodium concentration without clinical sequelae.
  • Mild metabolic alkalosis reflected by a modest increase in arterial pH.
  • Local irritation at the infusion site.

Serious

  • Severe metabolic alkalosis that may precipitate hypokalemia and muscle weakness.
  • Cardiac arrhythmias, including premature beats or tachyarrhythmias, linked to electrolyte disturbances.
  • Pulmonary edema resulting from rapid intravascular volume expansion.
  • Hypernatremia presenting with neurologic signs such as confusion, lethargy, or seizures.
  • Seizures directly attributable to extreme alkalosis and electrolyte imbalance.

Precautions & Warnings

When using Hospasol, clinicians should observe several precautionary measures to minimize risk and ensure appropriate patient selection.

  • Verify baseline arterial blood gas and electrolyte values before administration.
  • Avoid use in patients with known hypersensitivity to sodium bicarbonate or related compounds.
  • Use caution in individuals with congestive heart failure or fluid overload risk.
  • Adjust or withhold therapy in patients with severe renal impairment or uncontrolled hypertension.
  • Monitor serum sodium, potassium, and pH frequently during and after infusion.
  • Limit infusion rate to recommended clinical guidelines to prevent rapid pH shifts.
  • Ensure adequate ventilation to facilitate carbon dioxide elimination.

Avoid Interactions

Intravenous sodium hydrogen carbonate can interact with other medications or clinical conditions, requiring attention to avoid adverse outcomes.

Avoid

  • Concomitant use of strong acids or acidifying agents that counteract alkalinization.
  • High-dose loop diuretics that may exacerbate electrolyte disturbances.
  • Medications that prolong the QT interval when severe alkalosis is present.

Use with caution

  • Calcium channel blockers, as rapid pH changes can affect calcium binding.
  • Certain antibiotics (e.g., aminoglycosides) where altered pH may influence renal clearance.
  • Blood products, because bicarbonate may affect coagulation parameters.
  • Vasopressors, since volume shifts can modify hemodynamic response.

Frequently Asked Questions

Hospasol contains sodium hydrogen carbonate as its sole active pharmaceutical ingredient.

Hospasol is supplied as a sterile solution for intravenous (IV) administration.

Hospasol may be considered when rapid correction of metabolic acidosis, management of acid‑base disturbances, or buffering of large chloride loads is required, such as during surgery, critical care, or renal replacement therapy.

When given IV, sodium hydrogen carbonate dissociates into sodium and bicarbonate ions; the bicarbonate buffers excess hydrogen ions, forming carbonic acid that is converted to water and CO₂, thereby raising arterial pH.

Common adverse reactions include transient facial flushing, mild nausea or vomiting, a temporary increase in serum sodium, mild metabolic alkalosis, and possible local irritation at the infusion site.

Serious reactions can include severe metabolic alkalosis with hypokalemia, cardiac arrhythmias, pulmonary edema, hypernatremia with neurological symptoms, and seizures related to extreme alkalosis.

Baseline arterial blood gases, serum electrolytes (especially sodium and potassium), and renal function tests are recommended prior to infusion.

Caution is advised in patients with congestive heart failure or fluid overload because rapid volume expansion may exacerbate the condition.

Yes. It should be avoided with strong acids, high‑dose loop diuretics, and QT‑prolonging drugs. Use with caution when combined with calcium channel blockers, certain antibiotics, blood products, or vasopressors.

The regulatory status of Hospasol is not publicly specified, but it is generally considered a prescription‑only product in most jurisdictions.

Continuous monitoring of arterial pH, serum sodium, potassium, and overall fluid balance is recommended throughout the infusion and after completion.

Hospasol should be stored according to the manufacturer’s instructions, typically in a cool, dry place protected from light, and used before the expiration date indicated on the packaging.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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