Product image of Glucose (Glucose Monohydrate) supplied by GNH India

Glucose

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose (Glucose Monohydrate)

Glucose is a sterile solution for injection containing glucose monohydrate as the sole active ingredient. It is supplied in a liquid form intended for intravenous administration. The product is manufactured for the European market and is used as an energy substrate to raise blood glucose levels when rapid correction is required. As a parenteral carbohydrate, it supports cellular metabolism in clinical settings in hospital environments and emergency care.

Manufacturer / TM Owner

Fresenius Kabi Nederland B.V.

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Indications & Clinical Uses

Glucose injection is indicated for the rapid treatment of low blood sugar and for providing an immediate source of carbohydrate in various clinical situations.

  • Acute hypoglycemia in patients receiving insulin or oral hypoglycemic agents.
  • Energy support during surgery or anesthesia when oral intake is not possible.
  • Management of electrolyte imbalances that require carbohydrate supplementation.
  • Treatment of hyperkalemia as part of a regimen to shift potassium intracellularly.
  • Nutritional support in patients unable to tolerate enteral feeding.

Side Effects

Intravenous glucose may cause a range of reactions, most of which are mild and transient, while rare serious events can occur.

Common

  • Transient rise in blood glucose levels that typically normalize within hours.
  • Local discomfort, warmth, or irritation at the infusion site during administration.
  • Nausea, mild vomiting, or abdominal discomfort shortly after infusion.

Serious

  • Severe hyperglycemia leading to osmotic diuresis, dehydration, and electrolyte loss.
  • Allergic reactions ranging from skin rash and itching to full‑body anaphylaxis.
  • Pulmonary edema or cardiac arrhythmias in patients with underlying heart or fluid‑balance disorders.

Precautions & Warnings

When using intravenous glucose, clinicians should observe several precautions to minimize risks and ensure safe administration.

  • Verify patient’s blood glucose level before infusion to avoid overt hyperglycemia.
  • Adjust infusion rate in patients with renal or cardiac insufficiency to prevent fluid overload.
  • Monitor electrolytes, especially potassium, during and after administration.
  • Use aseptic technique to reduce risk of infection at the injection site.
  • Avoid rapid bolus administration in neonates and infants.
  • Assess for history of hypersensitivity to glucose solutions before use.

Avoid Interactions

Glucose injection can interact with other medications or clinical conditions, requiring careful consideration of concurrent therapies.

Avoid

  • Co‑administration with high‑dose insulin without monitoring, which may precipitate severe hypoglycemia.
  • Simultaneous infusion of hypertonic dextrose solutions, which can cause excessive hyperglycemia.

Use with caution

  • Concurrent use of potassium‑sparing diuretics, as rapid glucose infusion may shift potassium intracellularly.
  • Administration with beta‑adrenergic agonists, which can augment glucose release and affect blood sugar control.
  • Patients receiving total parenteral nutrition, requiring adjustment of carbohydrate content.

Frequently Asked Questions

Glucose injection delivers glucose directly into the bloodstream via the intravenous route, providing an immediate rise in blood sugar, whereas oral tablets must be absorbed through the gastrointestinal tract, resulting in a slower onset of action.

It is administered by a healthcare professional using a sterile IV line, with the infusion rate adjusted based on the patient’s blood glucose level, clinical condition, and physician orders.

The primary indications include acute hypoglycemia, providing carbohydrate support during surgery or anesthesia, treating hyperkalemia, and serving as part of parenteral nutrition for patients unable to eat orally.

When given intravenously, glucose can raise blood glucose concentrations within minutes, often normalizing hypoglycemia in 5 to 15 minutes depending on the dose and infusion rate.

Blood glucose should be measured frequently (e.g., every 15–30 minutes initially), and electrolytes, especially potassium, should be checked to detect any shifts caused by the infusion.

Yes, but dosing and infusion rates must be carefully calculated based on weight and clinical status, and rapid bolus administration is generally avoided in neonates and infants.

Signs may include rash, itching, swelling, shortness of breath, or anaphylaxis; any of these symptoms require immediate medical attention and discontinuation of the infusion.

Glucose stimulates insulin release, which drives potassium into cells and can lower serum potassium; therefore, potassium levels should be monitored, especially in patients at risk for hypokalemia.

Combining the two requires close monitoring; insulin may be needed to control hyperglycemia after glucose administration, but dosing must be individualized to avoid swings in blood sugar.

The product should be stored at controlled room temperature, protected from light, and used before the expiration date indicated on the packaging.

By providing glucose, insulin secretion is stimulated, which drives potassium into cells, thereby lowering extracellular potassium concentrations as part of hyperkalemia management.

Contraindications include known hypersensitivity to glucose solutions and conditions where rapid fluid administration could worsen fluid overload, such as severe heart failure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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