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Glukos Med Na40 + K20 Braun

Active Ingredient:
Potassium Chloride, Sodium Chloride, Glucose Monohydrate
Origin:
EU

Glukos Med Na40 + K20 Braun (Potassium Chloride, Sodium Chloride, Glucose Monohydrate)

Glukos Med Na40 + K20 Braun is an intravenous injection solution that combines potassium chloride, sodium chloride, and glucose monohydrate. Formulated for parenteral use, it delivers essential electrolytes and carbohydrate energy directly into the bloodstream. The product is manufactured for the EU market and is available by prescription only. It is intended to correct electrolyte disturbances, support fluid balance, and provide rapid glucose supplementation when needed.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Glukos Med Na40 + K20 Braun is indicated for several clinical situations that require rapid electrolyte and fluid replacement. It is commonly employed in hospital settings for patients who need intravenous support.

  • Treatment of hypokalemia (low potassium levels)
  • Management of hyponatremia (low sodium levels)
  • Peri‑operative fluid and electrolyte replacement during surgery
  • Replenishment of fluid loss after trauma or extensive burns
  • Correction of hypoglycemia when oral intake is not possible
  • Support of intravascular volume in patients with dehydration

Side Effects

Side effects may occur with any intravenous electrolyte solution. Most are mild and transient, but serious reactions are possible and require immediate medical attention.

Common

  • Mild irritation or pain at the injection site
  • Transient nausea or vomiting
  • Temporary headache
  • Mild increase in blood pressure
  • Mild hyperglycemia (elevated blood glucose)
  • Slight electrolyte imbalance if administered rapidly

Serious

  • Severe hyperkalemia leading to cardiac arrhythmia
  • Acute hypernatremia causing neurological symptoms
  • Anaphylactic or severe allergic reaction
  • Phlebitis or thrombophlebitis at the infusion site
  • Rapid fluid overload resulting in pulmonary edema

Precautions & Warnings

Glukos Med Na40 + K20 Braun should be used with careful clinical monitoring to avoid complications. Specific considerations include:

  • Verify patient electrolyte levels before and during therapy
  • Adjust infusion rate in patients with renal impairment or heart failure
  • Use caution in pregnant or breastfeeding individuals; data are limited
  • Avoid rapid bolus administration to reduce risk of hyperkalemia
  • Monitor blood glucose closely in diabetic patients
  • Ensure proper aseptic technique to prevent infection at the infusion site

Avoid Interactions

Concurrent medications can influence the safety and effectiveness of Glukos Med Na40 + K20 Braun. Interactions fall into two categories:

Avoid

  • Potassium-sparing diuretics (e.g., spironolactone) that may cause dangerous hyperkalemia
  • ACE inhibitors or ARBs combined with high potassium intake
  • Sodium bicarbonate solutions administered simultaneously, which can cause precipitation

Use with caution

  • Other intravenous electrolytes or fluids that may alter sodium/potassium balance
  • Insulin therapy, which can shift potassium into cells
  • Beta‑adrenergic agonists that affect serum potassium levels
  • Anticoagulants, as rapid infusion may affect coagulation parameters

Frequently Asked Questions

The product is designed to supply potassium, sodium, and glucose intravenously to correct electrolyte imbalances, provide energy, and restore intravascular volume.

It is commonly used for hypokalemia, hyponatremia, peri‑operative fluid replacement, fluid loss due to trauma or surgery, and hypoglycemia when oral intake is not feasible.

The solution is administered intravenously, typically through a controlled infusion pump to regulate the rate of delivery.

Patients should have regular checks of serum potassium, sodium, glucose, and overall fluid balance, as well as cardiac monitoring if high potassium doses are used.

Use in renal impairment requires dose adjustment and close monitoring of potassium and sodium levels to avoid accumulation.

Safety data in pregnancy are limited; clinicians should weigh potential benefits against risks and consider alternative therapies when possible.

Symptoms may include rash, itching, swelling, difficulty breathing, or anaphylaxis, and require immediate medical attention.

The infusion should be stopped, potassium levels re‑checked, and appropriate measures such as calcium gluconate or insulin therapy may be initiated under medical supervision.

Mixing with other solutions should be avoided unless compatibility has been confirmed, as precipitation or electrolyte disturbances can occur.

Store the product at controlled room temperature, protected from light, and keep the vial sealed until use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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