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

Natriumbikarbonat Fresenius Kabi

Active Ingredient:
Sodium Hydrogen Carbonate
Origin:
EU

Natriumbikarbonat Fresenius Kabi (Sodium Hydrogen Carbonate)

Sodium Hydrogen Carbonate, the active ingredient in Natriumbikarbonat Fresenius Kabi, is an excipient presented as a sterile solution for injection for intravenous use. It provides bicarbonate ions to raise plasma pH and correct metabolic acidosis, and is also employed to alkalinize urine in clinical settings.

GNH India supplies Natriumbikarbonat Fresenius Kabi as a licensed, GDP‑compliant product sourced from the European Union, delivering reliable batches to hospitals, transplant centres, oncology units and pharmacy chains worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support international distribution.

Manufacturer / TM Owner

Fresenius Kabi Ab

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Indications & Clinical Uses

  • Natriumbikarbonat is an intravenous electrolyte replenisher that addresses acid‑base disturbances.
  • Metabolic acidosis: rapidly raises plasma bicarbonate concentration to normalize pH in patients with acute or chronic acid accumulation.
  • Correction of acid‑base disturbances: provides buffering capacity during surgery, trauma or renal failure to maintain systemic homeostasis.
  • Alkalinization of urine: elevates urinary pH to enhance excretion of acidic drugs or prevent calcium‑oxalate stone formation.

How It Works

  • Sodium Hydrogen Carbonate dissociates in plasma to release bicarbonate ions, which combine with hydrogen ions to form carbonic acid that is rapidly converted to CO₂ and water via carbonic anhydrase. This buffering reaction raises extracellular pH, counteracting metabolic acidosis, while the increased bicarbonate diffuses into renal tubular fluid, raising urinary pH and promoting alkalinization.

Side Effects

Intravenous administration of sodium hydrogen carbonate may be associated with several adverse reactions, ranging from mild to serious.

Common Side Effects

  • Injection site pain: mild discomfort or erythema at the infusion site.
  • Hypernatremia: elevated serum sodium levels causing thirst or mild edema.
  • Metabolic alkalosis: excessive rise in blood pH leading to tingling or nausea.
  • Hypocalcemia: reduced calcium levels manifesting as muscle cramps.

Serious or Rare Side Effects

  • Volume overload: pulmonary edema in patients with compromised cardiac function.
  • Severe hyperkalemia: paradoxical increase in potassium in certain renal conditions.
  • Allergic reaction: anaphylaxis with rash, bronchospasm, or hypotension.
  • Intracellular shift of potassium: can precipitate arrhythmias.

Precautions & Warnings

Before using Natriumbikarbonat, clinicians should consider several safety and handling precautions.

  • Indication assessment: confirm metabolic acidosis or need for urine alkalinization before administration.
  • Electrolyte monitoring: regularly check serum sodium, potassium, and bicarbonate levels during therapy.
  • Cardiac status: avoid rapid infusion in patients with heart failure or fluid overload risk.
  • Renal function: adjust dose in severe renal impairment to prevent alkalosis.
  • Concomitant alkalinizing agents: limit use with other bicarbonate‑containing solutions to avoid over‑correction.
  • Store at ambient temperature: keep in original container, protect from light and moisture, and do not freeze.

Avoid Interactions

Sodium hydrogen carbonate can interact with other medicines, influencing electrolyte balance or drug efficacy.

Major Interactions (Avoid)

  • Calcium channel blockers: may potentiate hypotension when combined with rapid bicarbonate infusion.
  • Certain antibiotics (e.g., penicillins): high urinary pH can reduce drug stability and effectiveness.
  • Loop diuretics: increased risk of metabolic alkalosis and electrolyte disturbances.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: monitor potassium and renal function due to additive effects on electrolytes.
  • Antacids containing aluminum or magnesium: may cause precipitation or reduced absorption of other oral drugs.
  • Insulin therapy: rapid correction of acidosis can alter glucose utilization, requiring insulin dose adjustment.

Frequently Asked Questions

Natriumbikarbonat is an intravenous solution of sodium hydrogen carbonate used to correct metabolic acidosis, stabilize acid‑base balance during critical care, and alkalinize urine to aid the elimination of certain acidic substances or prevent stone formation.

After infusion, sodium hydrogen carbonate dissociates into sodium and bicarbonate ions. The bicarbonate buffers excess hydrogen ions, forming carbonic acid that is quickly converted to carbon dioxide and water, thereby raising blood pH and providing a buffering capacity that restores normal acid‑base status.

The dose of Natriumbikarbonat is determined by the prescribing clinician based on the patient’s acid‑base status, weight, renal function and clinical condition. Dosage calculations are individualized and should follow local prescribing guidelines.

Safety data for sodium hydrogen carbonate in pregnancy and lactation are limited. It should only be used when clearly needed and after a risk‑benefit assessment by the treating physician. Breastfeeding mothers should consult their healthcare provider before use.

To order, 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 required) and necessary import documentation.

Natriumbikarbonat provides direct bicarbonate ions, offering rapid correction of acidosis compared with oral alkali salts that require gastrointestinal absorption. It is preferred in acute settings where immediate pH adjustment is needed, whereas oral agents are used for chronic management.

Store at ambient temperature: keep the vial in its original packaging, protect from light and moisture, and do not freeze. Ensure the container remains sealed until use to maintain sterility.

Natriumbikarbonat is administered intravenously as a sterile solution. It is typically infused slowly under clinical supervision, with the infusion rate adjusted according to the patient’s electrolyte status and response to therapy.

Serious risks include volume overload leading to pulmonary edema, severe metabolic alkalosis, hypernatremia, and rare allergic reactions such as anaphylaxis. Continuous monitoring of fluid balance and electrolytes is essential to mitigate these risks.

Patients with uncontrolled heart failure, severe fluid overload, known hypersensitivity to sodium bicarbonate, or those receiving conflicting alkalinizing agents should not receive Natriumbikarbonat unless a careful risk assessment justifies its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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