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Glucosum Et Natrium Chloratum 2:1 Fresenius

Active Ingredient:
Sodium Chloride, Glucose Monohydrate
Origin:
EU

Glucosum Et Natrium Chloratum 2:1 Fresenius (Sodium Chloride, Glucose Monohydrate)

Glucosum Et Natrium Chloratum 2:1 Fresenius is an intravenous solution containing sodium chloride and glucose monohydrate in a 2:1 ratio. It is supplied as a sterile liquid for infusion, intended for fluid and electrolyte replacement in clinical settings. The product is manufactured in the European Union and requires a prescription. It is packaged in infusion bags and used under medical supervision to restore fluid volume and provide an energy substrate.

Manufacturer / TM Owner

Fresenius Kabi Polska Sp. Z O.O.

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Indications & Clinical Uses

Glucosum Et Natrium Chloratum 2:1 is indicated for clinical situations where rapid fluid and electrolyte replacement is required.

  • Rehydration of patients with dehydration due to vomiting, diarrhea, or excessive sweating.
  • Replacement of sodium and chloride losses in surgical or trauma patients.
  • Support of blood glucose levels in individuals at risk of hypoglycemia.
  • Maintenance of fluid balance during peri‑operative care or intensive‑care monitoring.
  • Adjunct therapy for electrolyte correction in metabolic disorders such as hyponatremia.

Side Effects

The safety profile of the solution reflects the components of sodium chloride and glucose, with most reactions being mild and related to the infusion process.

Common

  • Mild local irritation or erythema at the infusion site.
  • Transient increase in blood glucose concentration.
  • Slight electrolyte shifts causing mild nausea.
  • Low‑grade headache or dizziness during rapid infusion.

Serious

  • Hypernatremia leading to neurological symptoms.
  • Severe hyperglycemia, especially in diabetic patients.
  • Fluid overload with pulmonary edema.

Precautions & Warnings

Clinicians should evaluate patient-specific factors before administering Glucosum Et Natrium Chloratum 2:1 to minimize risks.

  • Assess baseline serum electrolytes and glucose before infusion.
  • Adjust infusion rate in patients with cardiac or renal impairment.
  • Avoid use in individuals with known hypersensitivity to sodium chloride or glucose solutions.
  • Monitor fluid balance and weight to prevent overload.
  • Use caution in pregnant or lactating women; limited safety data are available.
  • Do not mix with incompatible medications or solutions without compatibility testing.

Avoid Interactions

The solution may interact with other intravenous agents or affect the pharmacokinetics of certain drugs.

Avoid

  • Co‑administration with hypertonic saline solutions, which can cause excessive sodium load.
  • Simultaneous infusion of potassium‑containing preparations without electrolyte monitoring.

Use with caution

  • Concurrent use of insulin or oral hypoglycemics; monitor blood glucose closely.
  • Administration with nephrotoxic drugs; watch for altered renal handling of electrolytes.
  • Use alongside diuretics; electrolyte shifts may be amplified.

Frequently Asked Questions

It contains sodium chloride and glucose monohydrate in a 2:1 ratio, formulated as a sterile intravenous solution.

It is used when patients need rapid fluid and electrolyte replacement, such as after dehydration, surgery, trauma, or to prevent hypoglycemia.

Use in children should follow pediatric dosing guidelines and be supervised by a qualified healthcare professional.

Serum electrolytes, blood glucose, fluid balance, and vital signs should be monitored regularly throughout the infusion.

Compatibility should be confirmed before mixing; avoid co‑infusion with hypertonic saline or potassium solutions without proper monitoring.

Symptoms may include confusion, seizures, muscle twitching, or decreased level of consciousness.

Glucose provides an immediate energy substrate, helping to maintain blood sugar levels during periods of fasting or stress.

Yes, a slower infusion rate is recommended to reduce the risk of fluid overload in patients with cardiac compromise.

The solution should be stored at controlled room temperature, protected from light, and used before the expiration date.

Safety data are limited; it should only be used in pregnancy when clearly indicated and prescribed by a physician.

Mild irritation, erythema, or a transient feeling of warmth are the most frequently reported local reactions.

In addition to sodium chloride, it contains glucose, providing both electrolyte replacement and an energy source.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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