Product image of Kaliumklorid B. Braun (Potassium Chloride) supplied by GNH India

Kaliumklorid B. Braun

Active Ingredient:
Potassium Chloride
Origin:
EU

Kaliumklorid B. Braun (Potassium Chloride)

Potassium Chloride, the active ingredient in Kaliumklorid B. Braun, is an electrolyte / potassium supplement presented as an intravenous solution for intravenous use. It is employed to correct hypokalemia and to provide potassium replacement in patients requiring electrolyte management. It is indicated for adult patients with documented low serum potassium levels and is commonly used in intensive care, surgery, and dialysis settings.

GNH India supplies Kaliumklorid B. Braun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide. The company adheres to stringent quality standards and provides reliable logistics for global healthcare institutions.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Kaliumklorid B. Braun is used to address electrolyte disturbances, particularly low potassium levels, in various clinical settings.

  • Hypokalemia: restores serum potassium to normal range, supporting cardiac and muscular function.
  • Potassium replacement therapy: provides controlled potassium infusion for patients undergoing diuretic treatment or postoperative care.
  • Electrolyte imbalance during renal replacement therapy: helps maintain potassium balance in dialysis patients.

How It Works

  • Potassium chloride dissociates in plasma to release potassium ions, which increase extracellular potassium concentration. The elevated potassium restores the transmembrane gradient essential for the Na⁺/K⁺‑ATPase pump, stabilizing cellular membrane potential and enabling normal electrical activity in nerve, muscle and cardiac cells. Intravenous administration delivers the ion directly into the bloodstream for rapid correction of hypokalemia. This rapid increase helps prevent complications associated with severe potassium depletion.

Side Effects

Potassium chloride infusion can be associated with several adverse reactions, ranging from mild to serious.

Common Side Effects

  • Infusion site pain or irritation: discomfort at the catheter insertion point.
  • Nausea or vomiting: gastrointestinal upset following administration.
  • Mild hyperkalemia: transient elevation of serum potassium above normal.

Serious or Rare Side Effects

  • Cardiac arrhythmias: potentially life‑threatening rhythm disturbances.
  • Severe hyperkalemia: marked increase in serum potassium leading to cardiac arrest.
  • Anaphylactic reaction: rare hypersensitivity with respiratory compromise.

Precautions & Warnings

When using Kaliumklorid B. Braun, several precautions should be observed to ensure patient safety and product integrity.

  • Serum potassium assessment: verify baseline potassium levels before infusion.
  • Cardiac monitoring: observe ECG for arrhythmias during and after administration.
  • Renal function evaluation: adjust dose in patients with impaired kidney function.
  • Infusion rate control: avoid rapid administration exceeding recommended mEq per hour.
  • Concomitant drug review: caution with other potassium‑increasing agents.
  • Store at room temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Potassium chloride may interact with other medicines, affecting potassium balance or cardiac function.

Major Interactions (Avoid)

  • ACE inhibitors or ARBs: can cause additive hyperkalemia.
  • Potassium‑sparing diuretics (e.g., spironolactone): increase risk of severe hyperkalemia.
  • Trimethoprim‑containing antibiotics: potentiate potassium retention.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask symptoms of hyperkalemia‑induced arrhythmias.
  • Digoxin: elevated potassium can alter digoxin toxicity risk.

Frequently Asked Questions

Kaliumklorid B. Braun is an intravenous potassium chloride solution used to treat hypokalemia and to provide potassium replacement in patients with low serum potassium, such as those on diuretics, postoperative patients, or individuals undergoing dialysis.

Potassium chloride dissociates after infusion, releasing potassium ions that raise extracellular potassium levels. This restores the Na⁺/K⁺‑ATPase gradient, stabilizes cell membrane potential, and supports normal electrical activity in nerves, muscles, and the heart.

The prescribed dose is individualized by the treating physician based on the patient’s current serum potassium concentration, renal function, and overall clinical condition. The healthcare professional calculates the required milliequivalents and sets an appropriate infusion rate.

Safety data are limited. The product should be used in pregnancy or lactation only when the potential benefit to the mother outweighs any potential risk to the fetus or infant, and the decision rests with the prescriber after careful evaluation.

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 and the necessary import documentation.

Unlike oral potassium salts, the intravenous formulation provides rapid correction of serum potassium and is suitable for patients who cannot take oral medication. Oral preparations act more slowly and are generally used for maintenance therapy rather than acute correction.

The solution should be stored at controlled room temperature, protected from light and moisture, and kept in its original container until use. Do not freeze or shake the product before administration.

It is administered by intravenous infusion through a peripheral or central line under the supervision of qualified healthcare personnel. The infusion rate is set according to the prescribed dose and patient monitoring requirements.

The most critical risks include severe hyperkalemia leading to cardiac arrhythmias or arrest, and rare anaphylactic reactions. Continuous cardiac monitoring and regular serum potassium checks are essential to detect these complications early.

Patients with documented hyperkalemia, severe renal impairment without appropriate dose adjustment, or known hypersensitivity to potassium chloride should not be given this product. Clinicians must evaluate contraindications before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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