Product image of Kaliumklorid-Glukose Sad (Potassium Chloride, Glucose Monohydrate) supplied by GNH India

Kaliumklorid-Glukose Sad

Active Ingredient:
Potassium Chloride, Glucose Monohydrate
Origin:
EU

Kaliumklorid-Glukose Sad (Potassium Chloride, Glucose Monohydrate)

Potassium chloride and glucose monohydrate, the active ingredient in Kaliumklorid-Glukose Sad, is an electrolyte solution presented as an intravenous solution for intravenous use. It treats hypokalemia, supports fluid replacement and addresses hypoglycemia in hospitalized patients.

GNH India supplies Kaliumklorid-Glukose Sad as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Amgros I/S

1
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Indications & Clinical Uses

Kaliumklorid-Glukose Sad is used in fluid and electrolyte therapy to correct electrolyte imbalances and support metabolic needs.

  • Hypokalemia: restores potassium levels to prevent cardiac and muscular complications.
  • Fluid replacement: provides isotonic fluid to maintain intravascular volume in dehydration or postoperative states.
  • Hypoglycemia: supplies glucose to raise blood sugar and facilitate cellular energy while aiding potassium uptake.

How It Works

  • The solution delivers potassium ions directly into the bloodstream, raising serum potassium concentration and correcting hypokalemia. Glucose monohydrate supplies an immediate carbohydrate source, stimulating insulin release that promotes intracellular potassium shift and provides cellular energy. Together they re‑establish fluid and electrolyte balance when administered intravenously.

Side Effects

Kaliumklorid-Glukose Sad 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 sickness.
  • Hyperglycemia: elevated blood glucose levels, especially in diabetic patients.

Serious or Rare Side Effects

  • Cardiac arrhythmia: abnormal heart rhythm due to rapid potassium shifts.
  • Anaphylactic reaction: severe allergic response requiring immediate treatment.
  • Severe hyperkalemia: dangerous rise in potassium causing muscle weakness or cardiac arrest.

Precautions & Warnings

When using Kaliumklorid-Glukose Sad, clinicians should observe several precautions to ensure patient safety.

  • Renal impairment: monitor serum potassium and adjust infusion rate.
  • Cardiac disease: assess ECG before and during therapy.
  • Diabetes mellitus: watch blood glucose levels closely.
  • Concomitant potassium‑sparing drugs: avoid additive hyperkalemia risk.
  • Pediatric use: dose must be calculated carefully by the prescriber.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Kaliumklorid-Glukose Sad can interact with other medications, influencing potassium or glucose balance.

Major Interactions (Avoid)

  • ACE inhibitors or ARBs: may potentiate hyperkalemia.
  • Potassium‑sparing diuretics (e.g., spironolactone): increase risk of severe hyperkalemia.
  • Insulin therapy: concurrent high‑dose insulin can cause rapid intracellular potassium shift.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt insulin‑mediated potassium uptake.
  • Digoxin: elevated potassium can enhance digoxin toxicity.
  • Loop diuretics: may cause fluctuating potassium levels requiring monitoring.

Frequently Asked Questions

Kaliumklorid-Glukose Sad is an intravenous electrolyte solution used to correct low blood potassium (hypokalemia), provide fluid replacement in dehydrated or postoperative patients, and treat low blood sugar (hypoglycemia) by delivering glucose alongside potassium.

Potassium chloride supplies potassium ions that raise serum potassium levels, while glucose monohydrate provides a rapid source of carbohydrate that stimulates insulin release. Insulin promotes the movement of potassium into cells, helping to normalize electrolyte balance and supply cellular energy.

The dose of Kaliumklorid-Glukose Sad is individualized by the prescribing clinician based on the patient’s serum potassium, glucose levels, weight, renal function and overall clinical condition. No fixed regimen is provided; the prescriber determines the appropriate infusion rate and volume.

Safety data for Kaliumklorid-Glukose Sad in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

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 any cold‑chain needs) and import documentation.

Kaliumklorid-Glukose Sad combines potassium chloride with glucose, offering both potassium repletion and an immediate energy source. Compared with plain potassium chloride solutions, it may reduce the risk of hypoglycemia and facilitate intracellular potassium shift, while still providing the same electrolyte correction benefits.

Store Kaliumklorid-Glukose Sad at ambient temperature, preferably below 25 °C. Keep the container sealed, protect it from direct light and moisture, and avoid freezing. Follow standard aseptic handling procedures when preparing the IV infusion.

The product is administered intravenously. It is typically diluted in compatible IV fluids and infused over a period determined by the prescriber, with continuous monitoring of serum potassium, glucose, and cardiac rhythm as appropriate.

Serious risks include severe hyperkalemia leading to cardiac arrhythmia, anaphylactic reactions, and rapid shifts in blood glucose that may cause metabolic disturbances. Immediate medical attention is required if signs of cardiac irregularities, severe allergic response, or unexpected blood‑sugar changes occur.

Patients with known hypersensitivity to potassium chloride or glucose monohydrate, those with severe hyperkalemia, uncontrolled diabetes with high baseline glucose, or severe renal failure where potassium excretion is compromised should not receive this product unless closely monitored by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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