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Glucose Medipharm

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose Medipharm (Glucose Monohydrate)

Glucose Medipharm is a sterile injectable solution containing glucose monohydrate. It is supplied in an unspecified strength for the European market. Classified as a carbohydrate excipient for parenteral nutrition, it is prescription‑only. The formulation is designed for intravenous use to raise glucose levels and support fluid balance during treatment.

Manufacturer / TM Owner

Meditrade-Medipharm Gmbh

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Indications & Clinical Uses

Glucose Medipharm is indicated for several clinical situations where rapid carbohydrate delivery is required to correct low blood sugar, provide energy in parenteral nutrition, or assist with fluid management.

  • Treatment of documented hypoglycemia in hospital or emergency settings.
  • Component of total parenteral nutrition regimens for patients unable to receive enteral feeding.
  • Fluid replacement therapy when isotonic carbohydrate solutions are needed.
  • Support for patients undergoing surgery or critical illness who require controlled glucose infusion.
  • Adjunct in diagnostic procedures that require intravenous glucose loading.

Side Effects

Glucose Medipharm, like other intravenous carbohydrate solutions, may be associated with a range of adverse effects, most of which are related to its metabolic and osmotic properties.

Common

  • Transient increase in blood glucose levels.
  • Mild hyperosmolarity leading to temporary thirst.
  • Local irritation at the injection site.
  • Nausea or mild abdominal discomfort.

Serious

  • Severe hyperglycemia requiring insulin therapy.
  • Electrolyte disturbances such as hyponatremia.
  • Fluid overload with risk of pulmonary edema.
  • Allergic reactions ranging from rash to anaphylaxis.

Precautions & Warnings

When using Glucose Medipharm, clinicians should observe specific precautions to minimize risks and ensure appropriate therapeutic outcomes.

  • Verify blood glucose concentration before and during infusion.
  • Adjust infusion rate in patients with renal or cardiac insufficiency.
  • Monitor electrolyte levels, especially sodium and potassium, during prolonged therapy.
  • Use caution in individuals with diabetes mellitus or impaired glucose tolerance.
  • Avoid rapid infusion in neonates and small children due to risk of hyperosmolar injury.
  • Ensure compatibility with other intravenous solutions before co‑administration.

Avoid Interactions

Glucose Medipharm can interact with other medications or solutions, influencing glucose metabolism or fluid balance, therefore awareness of potential interactions is essential.

Avoid

  • Concurrent administration with high‑dose insulin without close glucose monitoring.
  • Mixing with calcium‑containing solutions that may precipitate.
  • Co‑infusion with hypertonic saline solutions that could exacerbate hyperosmolarity.

Use with caution

  • Concurrent use of diuretics that may alter electrolyte status.
  • Administration alongside beta‑blockers, which can mask hypoglycemia symptoms.
  • Co‑administration with other carbohydrate‑containing parenterals, requiring total glucose load calculation.

Frequently Asked Questions

Glucose Medipharm is a sterile solution for injection that contains glucose monohydrate as the active ingredient. It is supplied as an aqueous solution intended for intravenous administration.

The product is infused directly into a vein using a calibrated infusion set. The rate and total volume are determined by the patient’s clinical condition and blood glucose monitoring.

It is commonly prescribed for documented hypoglycemia, as part of total parenteral nutrition, and for fluid replacement when a carbohydrate source is needed.

Blood glucose levels, electrolyte concentrations, and fluid balance should be monitored regularly. Vital signs and signs of fluid overload are also assessed.

Use in neonates and small children should be cautious, with slower infusion rates and close monitoring to avoid hyperosmolar injury.

Glucose Medipharm provides an immediate intravenous source of glucose, bypassing gastrointestinal absorption, which is useful when oral intake is not possible or rapid correction is needed.

Common side effects include a transient rise in blood glucose, mild thirst from hyperosmolarity, local irritation at the injection site, and occasional nausea.

Discontinuation is advised if severe hyperglycemia, significant electrolyte imbalance, fluid overload, or an allergic reaction occurs.

There are no absolute contraindications listed, but it should be used with caution in patients with uncontrolled diabetes, severe renal or cardiac failure, and known hypersensitivity to glucose solutions.

Concurrent high‑dose insulin can cause rapid fluctuations in blood glucose; therefore, glucose levels must be closely monitored and insulin doses adjusted as needed.

Store the unopened vials in a cool, dry place protected from light. After opening, use according to the manufacturer’s aseptic guidelines and discard any remaining solution within the recommended time frame.

Compatibility should be confirmed before mixing; it is generally compatible with isotonic saline and dextrose solutions but may precipitate with calcium‑containing fluids.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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