Product image of Natriumwaterstofcarbonaat Fresenius Kabi Nederland (Sodium Hydrogen Carbonate) supplied by GNH India

Natriumwaterstofcarbonaat Fresenius Kabi Nederland

Active Ingredient:
Sodium Hydrogen Carbonate
Origin:
EU

Natriumwaterstofcarbonaat Fresenius Kabi Nederland (Sodium Hydrogen Carbonate)

Sodium hydrogen carbonate, the active ingredient in Natriumwaterstofcarbonaat Fresenius Kabi Nederland, is an electrolyte presented as a solution for injection for intravenous use. It supplies bicarbonate ions to buffer excess hydrogen ions, helping correct metabolic acidosis in patients who require acid‑base management, such as those in intensive care or undergoing major surgery.

GNH India supplies Natriumwaterstofcarbonaat Fresenius Kabi Nederland as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and intensive care units worldwide, including academic medical centres and private clinics.

Manufacturer / TM Owner

Fresenius Kabi Nederland B.V.

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Indications & Clinical Uses

Sodium hydrogen carbonate is employed to treat acid‑base disorders, primarily metabolic acidosis, by providing exogenous bicarbonate.

  • Metabolic acidosis: restores normal blood pH by increasing serum bicarbonate and neutralizing excess hydrogen ions.
  • Renal tubular acidosis: corrects systemic acidemia when endogenous bicarbonate reabsorption is impaired.
  • Diabetic ketoacidosis: supplies bicarbonate to support pH normalization in severe cases where acidosis persists despite insulin therapy.
  • Lactic acidosis: provides bicarbonate to buffer hydrogen ions generated from lactate accumulation in septic or hypoxic conditions.
  • Hyperchloremic acidosis: supplies bicarbonate to offset chloride‑induced reduction in plasma pH.

How It Works

  • Sodium hydrogen carbonate dissociates in plasma to yield sodium and bicarbonate ions. The bicarbonate acts as a physiological buffer, combining with hydrogen ions to form carbonic acid, which is rapidly converted to water and carbon dioxide for exhalation. This shift reduces the concentration of free hydrogen ions, raising blood pH toward normal. The administered sodium also contributes to extracellular fluid volume and electrolyte balance, supporting overall acid‑base homeostasis.

Side Effects

Sodium hydrogen carbonate may be associated with several adverse reactions, most of which are related to its electrolyte and alkalinizing properties.

Common Side Effects

  • Hypernatremia: serum sodium may increase, causing thirst, hypertension, or mild neurologic signs.
  • Fluid overload: excess volume can produce peripheral edema and increased cardiac workload.
  • Metabolic alkalosis: over‑correction may raise blood pH beyond the normal range.
  • Hypokalemia: potassium shift into cells may lead to muscle weakness or arrhythmias.
  • Infusion site irritation: redness, pain, or swelling at the injection site.

Serious or Rare Side Effects

  • Severe hypernatremia: marked sodium rise can cause confusion, seizures, or coma.
  • Pulmonary edema: fluid in lungs may cause dyspnea and reduced oxygenation.
  • Anaphylactic reaction: rare hypersensitivity with rash, bronchospasm, hypotension, and possible shock.
  • Severe metabolic alkalosis: profound pH elevation may precipitate cardiac arrhythmias and neuromuscular irritability.

Precautions & Warnings

When using sodium hydrogen carbonate injection, several precautions should be observed to ensure safe and effective therapy.

  • Monitor serum electrolytes: regularly check sodium, bicarbonate, and potassium levels during treatment.
  • Assess acid‑base status: obtain baseline arterial blood gas before infusion and repeat as needed.
  • Adjust infusion rate: avoid rapid administration that could over‑correct pH.
  • Use caution in renal impairment: reduced excretion may increase risk of electrolyte imbalance.
  • Contraindicated in severe metabolic alkalosis: do not administer when pH is already elevated.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Sodium hydrogen carbonate can interact with other medicines, influencing electrolyte balance or acid‑base status.

Major Interactions (Avoid)

  • Sodium bicarbonate + calcium carbonate: risk of hypercalcemia and excessive alkalinity.
  • Sodium bicarbonate + loop diuretics: may exacerbate electrolyte disturbances, especially hypokalemia.
  • Sodium bicarbonate + ACE inhibitors or ARBs: increased chance of metabolic alkalosis.

Moderate Interactions (Monitor Closely)

  • Sodium bicarbonate + potassium‑sparing diuretics: monitor potassium to prevent hyperkalemia.
  • Sodium bicarbonate + antacids: cumulative alkali load may require dose adjustment.
  • Sodium bicarbonate + insulin therapy: insulin‑induced potassium shift can be amplified.

Frequently Asked Questions

Sodium hydrogen carbonate injection is used to treat acid‑base disturbances, especially metabolic acidosis, by providing bicarbonate ions that help raise blood pH toward normal levels in hospitalized patients.

The solution dissociates into sodium and bicarbonate ions; bicarbonate buffers excess hydrogen ions, forming carbonic acid, which is then converted to water and carbon dioxide for exhalation, thereby reducing acidity.

The prescribed dose is individualized by the treating clinician based on the patient’s current acid‑base status, serum electrolyte values, underlying condition, and the desired rate of pH correction.

Safety data for sodium hydrogen carbonate injection in pregnancy and lactation are limited; it should be used only if the potential benefit justifies any potential risk to the fetus or infant.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

This injectable sodium hydrogen carbonate is a sterile, GMP‑manufactured solution designed for intravenous use, offering precise dosing and rapid systemic availability compared with oral or compounded bicarbonate forms, which may have slower absorption and variable bioavailability.

The product must be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze, shake vigorously, or expose to temperatures outside the recommended range.

Administration is performed intravenously by a qualified healthcare professional, typically via a controlled infusion pump or syringe, following aseptic technique and the dosing instructions provided by the prescriber.

Serious risks include severe hypernatremia, pulmonary edema, anaphylactic reactions, and profound metabolic alkalosis, all of which require immediate medical attention and may necessitate discontinuation of therapy.

Patients with known hypersensitivity to the product, those with severe metabolic alkalosis, uncontrolled hypertension, or significant fluid overload should not receive this injection unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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