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Glucose 5% Basi

Active Ingredient:
Glucose
Origin:
EU

Glucose 5% Basi (Glucose)

Glucose 5% Basi is an intravenous solution containing 5 % w/v glucose as the active ingredient. It is supplied as a sterile, isotonic carbohydrate solution intended for parenteral administration. The product is classified as a carbohydrate solution and is marketed in the European Union. It is prescribed by healthcare professionals for use in clinical settings where rapid glucose delivery or fluid replacement is required and electrolyte balance.

Manufacturer / TM Owner

Laboratórios Basi – Indústria Farmacêutica, S.A.

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Indications & Clinical Uses

Glucose 5% Basi is used in several clinical situations where a rapid source of carbohydrate or fluid replacement is needed.

  • Treatment of acute hypoglycemia in patients unable to take oral glucose.
  • Component of parenteral nutrition regimens to provide caloric support.
  • Fluid and electrolyte replacement during surgery or trauma.
  • Dilution medium for intravenous drug admixtures.
  • Maintenance of blood glucose levels during prolonged fasting.
  • Support for patients with metabolic disorders requiring controlled glucose infusion.

Side Effects

Glucose 5% Basi may be associated with a range of adverse reactions, most of which are mild and transient.

Common

  • Mild hyperglycemia when administered in excess.
  • Local irritation or pain at the infusion site.
  • Nausea or vomiting related to rapid glucose infusion.
  • Electrolyte shifts, particularly decreased serum potassium.
  • Transient headache due to rapid osmotic changes.
  • Mild metabolic acidosis in patients with impaired renal function.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Fluid overload causing pulmonary edema.
  • Allergic reactions such as urticaria or anaphylaxis.
  • Hyperosmolar hyperglycemic state in susceptible patients.
  • Hypoglycemia if glucose infusion is abruptly discontinued after prolonged use.
  • Severe electrolyte disturbances such as hypernatremia or hypocalcemia.

Precautions & Warnings

When prescribing Glucose 5% Basi, clinicians should consider several precautionary measures to ensure safe administration and minimize complications.

  • Assess baseline blood glucose levels and continue periodic monitoring during the infusion to avoid both hyperglycemia and hypoglycemia.
  • Monitor cumulative fluid input and output, particularly in patients with congestive heart failure or impaired renal function, to prevent fluid overload.
  • Adjust the infusion rate based on the patient’s electrolyte status, especially potassium and sodium levels, to reduce the risk of shifts.
  • Employ strict aseptic technique when accessing the intravenous line to minimize the risk of catheter-associated bloodstream infections.
  • Avoid rapid bolus administration unless clinically indicated, as sudden glucose spikes can precipitate metabolic disturbances.
  • Confirm compatibility with other intravenous drugs before co‑administration, as incompatibility may cause precipitation or loss of efficacy.
  • Evaluate pregnancy status; current safety information is limited, so use only when the potential benefit justifies the potential risk.

Avoid Interactions

Glucose 5% Basi can interact with other medications or clinical conditions, influencing its safety and effectiveness.

Avoid

  • Co‑administration with insulin infusions without appropriate dose adjustments, which may cause severe hypoglycemia.
  • Simultaneous infusion of potassium chloride solutions, as rapid glucose delivery can increase serum potassium and precipitate arrhythmias.

Use with caution

  • Concurrent use of diuretics that affect electrolyte balance; monitor potassium and sodium levels closely.
  • Administration with beta‑adrenergic agonists, which may enhance glycogenolysis and alter glucose requirements.
  • Use in patients receiving total parenteral nutrition containing other carbohydrate sources; adjust total glucose load to prevent hyperglycemia.

Frequently Asked Questions

Glucose 5% Basi contains glucose at a concentration of 5 % weight/volume (w/v), which means 5 grams of glucose per 100 mL of solution.

It is commonly used for treating acute hypoglycemia, as part of parenteral nutrition, for fluid and electrolyte replacement during surgery or trauma, and as a diluent for other intravenous medications.

Yes, it can be used in pediatric patients when indicated, but dosing and infusion rates must be individualized by a qualified healthcare professional.

Regular monitoring of blood glucose, serum electrolytes, and fluid balance is recommended to detect hyperglycemia, electrolyte shifts, or fluid overload.

Compatibility varies; it should be checked against each medication’s compatibility data before mixing to avoid precipitation or loss of efficacy.

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

The solution provides both water and an osmotic agent (glucose) that draws fluid into the vascular space, assisting in restoring intravascular volume.

Rapid infusion can shift electrolytes, especially potassium and sodium; monitoring and adjustment are necessary in at‑risk patients.

Safety data are limited; it should be used only when the potential benefit outweighs any potential risk to the fetus.

The infusion rate should be reduced or stopped, and appropriate measures such as insulin therapy may be considered under medical supervision.

Aseptic technique reduces the risk of catheter‑related bloodstream infections, which can be serious complications of intravenous therapy.

It is classified under ATC code B05BB01, which corresponds to carbohydrate solutions used for parenteral nutrition and fluid replacement.

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GNH India Pharmaceuticals Limited

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