Product image of Natriumhydrogencarbonat-Lösung Fresenius Kabi Deutschland (Sodium Hydrogen Carbonate) supplied by GNH India

Natriumhydrogencarbonat-Lösung Fresenius Kabi Deutschland

Active Ingredient:
Sodium Hydrogen Carbonate
Origin:
EU

Natriumhydrogencarbonat-Lösung Fresenius Kabi Deutschland (Sodium Hydrogen Carbonate)

Sodium hydrogen carbonate, the active ingredient in Natriumhydrogencarbonat-Lösung Fresenius Kabi Deutschland, is an alkalizing agent presented as a solution for injection for intravenous use. It is employed to correct metabolic acidosis, assist in severe hyperkalemia management, and alkalinize urine in various acid‑base disorders.
GNH India supplies Natriumhydrogencarbonat-Lösung Fresenius Kabi Deutschland as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Fresenius Kabi Deutschland Gmbh

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Indications & Clinical Uses

Sodium hydrogen carbonate is used in clinical settings to address disorders of acid‑base balance and related electrolyte disturbances.

  • Metabolic acidosis: raises systemic pH by providing bicarbonate ions, helping restore normal acid‑base status.
  • Severe hyperkalemia (as part of therapy): shifts potassium into cells and supports cardiac stability when combined with other measures.
  • Alkalinization of urine: increases urinary pH to promote excretion of certain toxins or to prevent crystal formation.

How It Works

  • Sodium hydrogen carbonate dissociates to release bicarbonate ions, which combine with excess hydrogen ions in the bloodstream to form carbonic acid. This reaction is catalyzed by carbonic anhydrase, ultimately producing water and carbon dioxide that are exhaled, thereby raising systemic pH and correcting metabolic acidosis.

Side Effects

Adverse reactions may occur with intravenous administration of sodium hydrogen carbonate.

Common Side Effects

  • Mild pain or irritation at the injection site.
  • Transient hypernatremia due to sodium load.
  • Mild metabolic alkalosis if over‑corrected.
  • Fluid overload in patients with limited cardiac reserve.
  • Hypokalemia secondary to intracellular potassium shift.

Serious or Rare Side Effects

  • Severe metabolic alkalosis leading to respiratory depression.
  • Pulmonary edema in volume‑overloaded patients.
  • Cardiac arrhythmias from electrolyte disturbances.
  • Severe hypernatremia causing neurologic symptoms.
  • Anaphylactoid reactions (rare).

Precautions & Warnings

When using sodium hydrogen carbonate injection, clinicians should observe several safety measures.

  • Assess acid‑base status: verify indication and baseline pH before infusion.
  • Monitor electrolytes: check serum sodium, potassium, and calcium regularly.
  • Adjust infusion rate: administer slowly to avoid rapid pH shifts.
  • Caution in heart failure: limit volume to prevent overload.
  • Avoid in severe hypocalcemia: may exacerbate calcium deficiency.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Sodium hydrogen carbonate can influence the activity of other medications.

Major Interactions (Avoid)

  • Concurrent alkalinizing agents (e.g., other bicarbonate solutions) – risk of severe alkalosis.
  • Calcium‑containing IV solutions – may precipitate calcium carbonate.
  • Certain antibiotics (e.g., tetracyclines, fluoroquinolones) – reduced absorption/effectiveness.

Moderate Interactions (Monitor Closely)

  • Potassium supplements – may cause rapid shifts in serum potassium.
  • Loop diuretics – enhanced electrolyte loss requiring monitoring.
  • ACE inhibitors or ARBs – increased risk of hyperkalemia when combined with other therapies.
  • Digitalis glycosides – electrolyte changes can predispose to toxicity.

Frequently Asked Questions

Natriumhydrogencarbonat-Lösung is an intravenous sodium bicarbonate solution used to correct metabolic acidosis, assist in the management of severe hyperkalemia, and alkalinize urine in various acid‑base disorders.

When administered, sodium hydrogen carbonate dissociates into sodium and bicarbonate ions. The bicarbonate binds excess hydrogen ions, forming carbonic acid, which is rapidly converted to water and carbon dioxide, thereby raising systemic pH and correcting acidosis.

The dosage of Natriumhydrogencarbonat-Lösung is determined by the prescribing clinician based on the patient’s acid‑base status, electrolyte levels, and clinical condition. No standard dose is provided here.

Safety data for sodium hydrogen carbonate in pregnancy and lactation are limited. Use only if the potential benefit justifies any potential risk to the fetus or infant, and follow the prescriber’s guidance.

To place an 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 needed), and import documentation.

Sodium hydrogen carbonate is a rapid‑acting, readily available alkalinizing agent that directly supplies bicarbonate ions, unlike oral antacids which act more slowly. Compared with other IV alkalinizers, it has a well‑characterized safety profile but requires careful monitoring of electrolytes and volume status.

Store the solution at room temperature, preferably below 25 °C. Keep it in the original packaging, protect from moisture and direct sunlight, and ensure the vial is sealed until use.

The solution is administered intravenously, typically via a controlled infusion. The rate and total volume are set by the prescriber according to the patient’s laboratory values and clinical response.

Serious risks include severe metabolic alkalosis, pulmonary edema from fluid overload, significant electrolyte disturbances such as hypernatremia or hypokalemia, and rare anaphylactoid reactions. Continuous monitoring is essential during therapy.

Patients with known hypersensitivity to sodium bicarbonate, severe hypocalcemia, uncontrolled heart failure, or those who cannot tolerate rapid shifts in pH or volume should not receive this product unless a clinician determines it is absolutely necessary.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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