Product image of Kalii Chloridum/Natrii Chloridum B. Braun (Potassium Chloride, Sodium Chloride) supplied by GNH India

Kalii Chloridum/Natrii Chloridum B. Braun

Active Ingredient:
Potassium Chloride, Sodium Chloride
Origin:
EU

Kalii Chloridum/Natrii Chloridum B. Braun (Potassium Chloride, Sodium Chloride)

Potassium chloride and sodium chloride, the active ingredients in Kalii Chloridum/Natrii Chloridum B. Braun, are electrolyte supplements presented as an injection solution for intravenous use. They are employed to correct electrolyte depletion, such as hypokalemia and hyponatremia, in hospitalized patients who require rapid fluid and ion balance restoration.

GNH India supplies Kalii Chloridum/Natrii Chloridum B. Braun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Kalii Chloridum/Natrii Chloridum B. Braun is an intravenous electrolyte supplement used to address disorders of potassium and sodium balance.

  • Electrolyte depletion: restores normal potassium and sodium concentrations in patients with overall electrolyte loss.
  • Hypokalemia: raises low serum potassium levels to prevent cardiac and muscular complications.
  • Hyponatremia: increases serum sodium to correct dilutional hyponatremia.
  • Fluid replacement: provides essential ions as part of volume resuscitation in acute care settings.

How It Works

  • The injection delivers potassium and sodium ions directly into the bloodstream, increasing extracellular concentrations of these electrolytes. Elevated potassium supports cellular membrane potential and cardiac electrophysiology, while sodium contributes to osmotic balance and fluid distribution. Together they help re‑establish electrolyte homeostasis and maintain intravascular volume, facilitating normal nerve impulse transmission and muscle contraction.

Side Effects

Adverse reactions may occur with intravenous electrolyte administration.

Common Side Effects

  • Mild vein irritation at the infusion site.
  • Transient nausea or vomiting.
  • Temporary headache.
  • Mild dizziness.
  • Slight increase in blood pressure.
  • Mild muscle cramps.

Serious or Rare Side Effects

  • Hyperkalemia leading to cardiac arrhythmia.
  • Hypernatremia causing neurological disturbances.
  • Severe allergic reaction (anaphylaxis).
  • Phlebitis or thrombophlebitis.
  • Electrolyte imbalance with metabolic acidosis.
  • Renal impairment exacerbation.

Precautions & Warnings

When using Kalii Chloridum/Natrii Chloridum B. Braun, clinicians should consider several safety measures.

  • Patient assessment: evaluate baseline electrolyte levels and renal function before administration.
  • Infusion rate: avoid rapid infusion to reduce risk of cardiac events.
  • Monitoring: continuously monitor cardiac rhythm and serum electrolytes during therapy.
  • Contraindications: do not use in patients with known hypersensitivity to the formulation.
  • Compatibility: ensure compatibility with other IV solutions before mixing.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Electrolyte therapy can interact with other medications, requiring careful review.

Major Interactions (Avoid)

  • ACE inhibitors or ARBs: may potentiate hyperkalemia.
  • Potassium‑sparing diuretics: increase risk of elevated serum potassium.
  • Sodium‑containing medications: can exacerbate hypernatremia.

Moderate Interactions (Monitor Closely)

  • Digoxin: altered potassium levels affect digoxin toxicity.
  • NSAIDs: may impair renal excretion of electrolytes.
  • Insulin: shifts potassium intracellularly, requiring electrolyte monitoring.

Frequently Asked Questions

Kalii Chloridum/Natrii Chloridum B. Braun is an intravenous electrolyte solution containing potassium chloride and sodium chloride. It is used to correct electrolyte deficiencies such as hypokalemia and hyponatremia, and to support fluid replacement in patients who need rapid restoration of potassium and sodium balance.

The injection delivers potassium and sodium ions directly into the bloodstream, raising extracellular concentrations of these electrolytes. Potassium helps maintain cellular membrane potential and cardiac rhythm, while sodium contributes to osmotic balance and fluid distribution. Together they re‑establish electrolyte homeostasis and support normal physiological functions.

The dose of Kalii Chloridum/Natrii Chloridum B. Braun is determined by the prescribing clinician based on the patient’s electrolyte levels, clinical condition, and renal function. The healthcare professional will calculate the appropriate volume and concentration required for safe and effective therapy.

Safety data for Kalii Chloridum/Natrii Chloridum B. Braun in pregnancy and lactation are limited. Use only if clearly needed and after a risk‑benefit assessment by the treating physician. The prescriber should consider maternal and fetal electrolyte requirements before administration.

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 submission, the sales team will verify trade or institutional credentials and respond with pricing, availability, shipping details (including cold‑chain if required) and import documentation.

Kalii Chloridum/Natrii Chloridum B. Braun provides a combined potassium and sodium formulation in a single IV solution, which can simplify dosing compared with separate potassium or sodium preparations. It offers rapid correction of both electrolytes simultaneously, whereas other products may target only one ion or require multiple infusions.

The injection should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Before use, inspect the vial for particulate matter or discoloration and allow it to reach room temperature if required by the administration protocol.

Kalii Chloridum/Natrii Chloridum B. Braun is administered intravenously. The solution is typically diluted in an appropriate compatible IV fluid and infused over a controlled period, as directed by the prescribing clinician, to avoid rapid shifts in electrolyte concentrations.

Serious risks include hyperkalemia, which can cause life‑threatening cardiac arrhythmias, and hypernatremia, which may lead to neurological complications. Anaphylactic reactions, severe vein irritation, and renal impairment exacerbation are also possible and require immediate medical attention.

Patients with known hypersensitivity to potassium chloride, sodium chloride, or any component of the formulation should not receive this injection. It is also contraindicated in individuals with severe renal failure, uncontrolled hyperkalemia, or uncontrolled hypernatremia unless closely monitored by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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