Product image of Kaliumchlorid/Natriumchlorid B. Braun (Potassium Chloride, Sodium Chloride) supplied by GNH India

Kaliumchlorid/Natriumchlorid B. Braun

Active Ingredient:
Potassium Chloride, Sodium Chloride
Origin:
EU

Kaliumchlorid/Natriumchlorid B. Braun (Potassium Chloride, Sodium Chloride)

Potassium chloride and sodium chloride, the active ingredients in Kaliumchlorid/Natriumchlorid B. Braun, are electrolyte solutions presented as an intravenous solution for intravenous use. They restore deficient potassium and sodium ions, helping to correct hypokalemia, hyponatremia, and support overall fluid and electrolyte balance in hospitalized patients requiring careful monitoring in clinical settings. Administration is performed under physician supervision to ensure safe electrolyte correction.

GNH India supplies Kaliumchlorid/Natriumchlorid B. Braun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and clinics worldwide.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Kaliumchlorid/Natriumchlorid B. Braun is used as an intravenous electrolyte solution to correct specific ion deficiencies.

  • Electrolyte replacement: restores potassium and sodium levels in patients with overall electrolyte depletion.
  • Hypokalemia: raises low serum potassium concentrations to normal range.
  • Hyponatremia: increases serum sodium to correct dilutional hyponatremia.
  • Fluid and electrolyte balance maintenance: supports ongoing fluid therapy in postoperative or critically ill patients.

How It Works

  • Kaliumchlorid/Natriumchlorid delivers potassium (K⁺) and sodium (Na⁺) ions directly into the bloodstream via intravenous infusion. The added ions shift extracellular electrolyte concentrations, promoting osmotic balance and membrane potential restoration. Potassium repletion facilitates cellular repolarization, while sodium contributes to extracellular fluid volume and nerve impulse transmission, collectively correcting deficits and supporting normal physiological functions.

Side Effects

Kaliumchlorid/Natriumchlorid may be associated with several adverse reactions, ranging from mild to severe.

Common Side Effects

  • Injection site pain: mild discomfort at the infusion site.
  • Phlebitis: inflammation of the vein used for administration.
  • Nausea: transient feeling of queasiness.
  • Hyperkalemia: elevated serum potassium if infused rapidly.

Serious or Rare Side Effects

  • Cardiac arrhythmia: irregular heart rhythm due to electrolyte imbalance.
  • Severe hyperkalemia: life‑threatening potassium excess causing muscle weakness.
  • Anaphylactic reaction: rare hypersensitivity with rash, bronchospasm, or hypotension.

Precautions & Warnings

When using Kaliumchlorid/Natriumchlorid, clinicians should observe specific precautions to minimize risks.

  • Patient assessment: evaluate serum potassium and sodium levels before initiation.
  • Infusion rate: administer at a controlled rate to avoid rapid electrolyte shifts.
  • Cardiac monitoring: observe ECG for arrhythmias during and after infusion.
  • Concomitant drugs: adjust dosage when used with other potassium‑sparing agents or diuretics.
  • Renal function: assess kidney function as impaired clearance may increase risk of accumulation.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Kaliumchlorid/Natriumchlorid can interact with other medications, influencing electrolyte balance or cardiac function.

Major Interactions (Avoid)

  • ACE inhibitors or ARBs: may potentiate hyperkalemia.
  • Potassium‑sparing diuretics (e.g., spironolactone): increase risk of severe hyperkalemia.
  • Sodium‑containing IV fluids: can cause hypernatremia if combined excessively.

Moderate Interactions (Monitor Closely)

  • Digoxin: electrolyte shifts can alter its therapeutic window.
  • Beta‑blockers: may mask signs of hypoglycemia in patients with electrolyte disturbances.
  • NSAIDs: can impair renal excretion of potassium, requiring monitoring.

Frequently Asked Questions

Kaliumchlorid/Natriumchlorid is an intravenous electrolyte solution used to replace deficient potassium and sodium ions. It is indicated for treating hypokalemia, hyponatremia, and for maintaining fluid and electrolyte balance in patients who require intravenous therapy, such as those in intensive care or postoperative settings.

Potassium chloride provides potassium ions that enter the extracellular fluid after intravenous infusion. The increased potassium concentration helps restore normal cellular membrane potential, supports nerve impulse transmission, and promotes proper muscle function, thereby correcting low serum potassium levels.

The dose of Kaliumchlorid/Natriumchlorid is individualized. A prescriber determines the amount and infusion rate based on the patient’s laboratory values, clinical condition, and overall fluid management plan. No standard dosing regimen is provided in public literature.

Safety data for use in pregnancy or lactation are limited. The product should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and it must be prescribed and monitored by a qualified healthcare professional.

To order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide. After verification of trade or institutional credentials, the sales team will provide pricing, availability, shipping details (including any cold‑chain requirements), and assist with import documentation.

Kaliumchlorid/Natriumchlorid combines both potassium and sodium chloride in a single IV formulation, offering convenience over separate potassium chloride or sodium chloride preparations. It provides balanced electrolyte replacement in one bag, reducing the need for multiple infusions, but clinicians must still monitor serum levels closely, as with any electrolyte therapy.

The product must be stored refrigerated at 2‑8 °C. Keep the container in its original packaging, protect it from light, and avoid freezing or shaking the solution. If the temperature rises above the recommended range, discard the product according to local regulations.

It is administered intravenously, typically via a controlled infusion pump or gravity drip under physician supervision. The infusion rate is adjusted based on the patient’s electrolyte status and clinical response, and continuous cardiac monitoring is recommended during and after administration.

Serious risks include severe hyperkalemia or hypernatremia, which can lead to cardiac arrhythmias, muscle weakness, or neurological symptoms. Anaphylactic reactions, although rare, may also occur. Prompt recognition and management of these events are essential to patient safety.

The product is contraindicated in patients with known hyperkalemia, severe renal impairment that limits potassium excretion, or uncontrolled hypernatremia. Caution is also advised for individuals receiving other potassium‑containing medications or those with conditions predisposing them to rapid electrolyte shifts.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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