Product image of Glucose/Sodium Chloride Fresenius Kabi (Sodium Chloride, Glucose Monohydrate) supplied by GNH India

Glucose/Sodium Chloride Fresenius Kabi

Active Ingredient:
Sodium Chloride, Glucose Monohydrate
Origin:
EU

Glucose/Sodium Chloride Fresenius Kabi (Sodium Chloride, Glucose Monohydrate)

Glucose/Sodium Chloride Fresenius Kabi is an intravenous injection solution containing sodium chloride and glucose monohydrate. It is supplied as a sterile liquid for infusion, intended for use in the European Union market. It provides both electrolyte (sodium chloride) and carbohydrate (glucose) components to support fluid balance and energy needs when administered by healthcare professionals under prescription. It is designed for intravenous administration and classified as a prescription medication.

Manufacturer / TM Owner

Fresenius Kabi S.R.O.

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Indications & Clinical Uses

Glucose/Sodium Chloride injection is used in clinical settings to address fluid and electrolyte deficits and to provide an energy source during intravenous therapy.

  • Replenishment of extracellular fluid volume in patients with dehydration or hypovolemia.
  • Replacement of sodium and chloride losses associated with gastrointestinal drainage, burns, or diuretic therapy.
  • Provision of a carbohydrate source for patients unable to receive oral nutrition.
  • Support of perioperative fluid management to maintain hemodynamic stability.
  • Adjunctive therapy in parenteral nutrition regimens where glucose is required.

Side Effects

Adverse reactions to Glucose/Sodium Chloride injection are generally infrequent, but they may occur and are categorized by frequency and severity.

Common

  • Mild local irritation at the infusion site.
  • Transient hyperglycemia.
  • Slight increase in serum sodium levels.
  • Nausea or mild headache.

Serious

  • Severe hypernatremia leading to neurologic symptoms.
  • Anaphylactic or severe allergic reaction.
  • Fluid overload causing pulmonary edema.

Precautions & Warnings

When administering Glucose/Sodium Chloride injection, clinicians should observe several precautions to minimize risk and ensure appropriate use.

  • Assess patient’s fluid status and electrolyte balance before initiation.
  • Monitor serum glucose and sodium concentrations during therapy.
  • Use caution in patients with renal impairment or congestive heart failure.
  • Adjust infusion rate in individuals at risk for rapid shifts in osmolarity.
  • Avoid administration to patients with known hypersensitivity to any component of the solution.
  • Consider compatibility with other intravenous medications before co‑infusion.

Avoid Interactions

Glucose/Sodium Chloride injection may interact with other drugs; awareness of these interactions helps prevent adverse outcomes.

Avoid

  • Concurrent administration with hypertonic saline solutions, which may cause excessive sodium load.
  • Mixing with calcium‑containing solutions that can precipitate insoluble salts.

Use with caution

  • Concurrent use of insulin or oral hypoglycemic agents, which may amplify glucose‑lowering effects.
  • Diuretics that promote sodium loss, requiring close monitoring of electrolyte status.
  • Blood pressure–lowering agents, as rapid volume expansion may affect hemodynamics.

Frequently Asked Questions

The product contains sodium chloride and glucose monohydrate dissolved in a sterile aqueous solution for intravenous use.

It is used to replace fluid volume, restore sodium and chloride balance, and provide a carbohydrate source for patients who cannot take oral nutrition.

The solution is administered intravenously by a healthcare professional, usually through a peripheral or central venous catheter.

Compatibility should be checked before co‑infusion; some calcium‑containing solutions may precipitate, and hypertonic saline should be avoided.

Serum glucose, sodium, and overall fluid balance should be monitored, especially in patients with renal or cardiac conditions.

Use in children should be determined by a physician, taking into account age‑specific fluid and electrolyte requirements.

Common side effects include mild local irritation at the infusion site, transient hyperglycemia, slight increases in serum sodium, nausea, or mild headache.

Serious reactions may include severe hypernatremia, anaphylactic or severe allergic responses, and fluid overload leading to pulmonary edema.

Insulin or other glucose‑lowering agents should be used with caution, as the glucose in the solution can affect blood sugar control.

The solution is contraindicated in patients with known hypersensitivity to sodium chloride, glucose monohydrate, or any excipients in the formulation.

It is a prescription‑only medication and must be administered under the supervision of a qualified healthcare professional.

Additional details are available on the Fresenius Kabi website or through the product’s prescribing information.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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