Product image of Glucosio S.A.L.F. (Glucose Monohydrate) supplied by GNH India

Glucosio S.A.L.F.

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucosio S.A.L.F. (Glucose Monohydrate)

Glucosio S.A.L.F. is a parenteral carbohydrate solution whose active ingredient is glucose monohydrate, supplied as a sterile solution for injection. The product is manufactured in the European Union and is classified as a carbohydrate solution/excipient used as an adjunct in parenteral nutrition. It is intended for intramuscular, intravenous, or subcutaneous administration to provide an immediate source of glucose and to assist in maintaining osmotic balance during fluid therapy.

Manufacturer / TM Owner

S.A.L.F. Spa Laboratorio Farmacologico

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Indications & Clinical Uses

Glucosio S.A.L.F. is employed in clinical settings where rapid glucose supplementation or fluid balance is required.

  • Treatment of documented hypoglycemia when oral glucose is not feasible.
  • Component of parenteral nutrition regimens for patients unable to receive enteral feeding.
  • Support for fluid and electrolyte replacement in perioperative or trauma care.
  • Provision of an energy substrate during prolonged fasting or critical illness.
  • Adjunct in neonatal intensive care to maintain glucose homeostasis.
  • Use in surgical patients to prevent peri‑operative hypoglycemia.

Side Effects

Adverse reactions to Glucosio S.A.L.F. are generally related to the glucose load and the route of administration.

Common

  • Transient hyperglycemia, especially in patients with impaired insulin response.
  • Local irritation or pain at the injection site.
  • Mild nausea or vomiting following rapid infusion.
  • Electrolyte shifts such as mild hyponatremia due to osmotic effects.
  • Headache associated with rapid changes in blood glucose.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Allergic or anaphylactic reaction to excipients.
  • Volume overload causing pulmonary edema in susceptible individuals.
  • Severe hypoglycemia if glucose is administered after insulin without monitoring.
  • Life‑threatening electrolyte disturbances (e.g., severe hyponatremia).

Precautions & Warnings

When using Glucosio S.A.L.F., clinicians should observe several precautions to minimize risk and ensure appropriate therapy.

  • Verify blood glucose level before and after administration to avoid over‑correction.
  • Adjust dose in patients with renal or hepatic impairment due to altered glucose metabolism.
  • Monitor fluid balance closely in patients at risk for volume overload or heart failure.
  • Use caution in individuals with known hypersensitivity to any component of the solution.
  • Limit infusion rate according to manufacturer guidelines to reduce the chance of hyperglycemia.
  • Consider alternative carbohydrate sources for patients with uncontrolled diabetes mellitus.
  • Ensure aseptic technique to prevent contamination of the injection solution.

Avoid Interactions

Glucosio S.A.L.F. may interact with other medications or clinical conditions that affect glucose homeostasis or fluid balance.

Avoid

  • Concomitant use of high‑dose insulin without glucose monitoring, which can precipitate severe hypoglycemia.
  • Co‑administration with other hypertonic glucose solutions, increasing risk of hyperglycemia and osmotic complications.
  • Use with diuretics in patients prone to electrolyte disturbances without close monitoring.

Use with caution

  • Concurrent administration of corticosteroids, which can raise blood glucose levels.
  • Beta‑blockers that may mask symptoms of hypoglycemia.
  • Medications that affect renal function, such as ACE inhibitors, requiring careful fluid assessment.
  • Anticoagulants, as rapid infusion may affect coagulation parameters.
  • Drugs that alter electrolyte balance, like potassium‑sparing agents.

Frequently Asked Questions

The active ingredient is glucose monohydrate, a simple carbohydrate used to provide energy.

It can be given intramuscularly, intravenously, or subcutaneously as a sterile solution for injection.

It is indicated for treatment of hypoglycemia, fluid and electrolyte replacement, and as an adjunct in parenteral nutrition.

It may be used in pediatric and neonatal care under strict medical supervision to maintain glucose homeostasis.

Blood glucose levels, electrolyte status, and fluid balance should be monitored before, during, and after infusion.

Allergic reactions are rare but possible; signs include rash, itching, swelling, or anaphylaxis and require immediate medical attention.

Glucosio S.A.L.F. provides rapid, controlled delivery of glucose directly into the bloodstream, useful when oral administration is not feasible.

Patients with heart failure should be monitored for volume overload, as the solution adds fluid to the circulatory system.

It can be combined, but glucose and insulin doses must be carefully balanced to avoid severe hypoglycemia or hyperglycemia.

The regulatory status varies by country; in many regions it is prescription‑only, but specific status should be confirmed locally.

Store the solution at controlled room temperature, protected from light, and discard after the expiration date.

The glucose in the solution contributes to the osmolarity of plasma, helping to maintain fluid distribution across compartments.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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