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Glucosa Altan

Active Ingredient:
Glucose, Anhydrous
Origin:
EU

Glucosa Altan (Glucose, Anhydrous)

Glucosa Altan is an intravenous solution that contains glucose, anhydrous as its sole active ingredient. The product is supplied in a sterile liquid form, with strength not specified, and is marketed in the European Union. It is classified as an excipient used to provide a source of carbohydrate and fluid during intravenous therapy. Glucosa Altan is intended for use under professional medical supervision in clinical settings.

Manufacturer / TM Owner

Altan Pharmaceuticals S.A.

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Indications & Clinical Uses

Glucosa Altan is employed in clinical practice primarily as an intravenous carbohydrate source and fluid supplement. It is indicated for a range of therapeutic situations where rapid glucose delivery is required.

  • Provide an immediate source of glucose for patients unable to eat orally.
  • Maintain blood sugar levels during perioperative or critical‑care situations.
  • Serve as a diluent for compatible intravenous medications.
  • Support fluid balance when combined with electrolytes.
  • Used in pediatric and adult settings under physician direction.

Side Effects

Side effects associated with Glucosa Altan are generally related to the intravenous administration of a glucose solution. Both common and rare reactions have been reported in clinical use.

Common

  • Transient hyperglycemia that resolves without intervention.
  • Mild irritation or pain at the infusion site.
  • Temporary increase in urine output due to osmotic diuresis.
  • Slight elevation of serum sodium when mixed with saline.

Serious

  • Severe hyperglycemia leading to metabolic acidosis.
  • Allergic reaction presenting as rash, itching, or hives.
  • Fluid overload causing pulmonary edema in susceptible patients.
  • Electrolyte imbalance, particularly hyponatremia, with large-volume infusions.

Precautions & Warnings

When using Glucosa Altan, healthcare professionals should observe several precautionary measures to ensure patient safety and optimal therapeutic outcomes.

  • Verify patient’s blood glucose level before initiating the infusion.
  • Adjust infusion rate in patients with diabetes or impaired glucose tolerance.
  • Monitor for signs of fluid overload, especially in cardiac or renal disease.
  • Use aseptic technique to prevent catheter‑related infections.
  • Avoid rapid administration in neonates and infants.
  • Document total volume and concentration administered in the medical record.

Avoid Interactions

Glucosa Altan may interact with other intravenous agents or medications that affect glucose metabolism, fluid balance, or electrolyte status. Awareness of these interactions helps prevent adverse events.

Avoid

  • Co‑administration with high‑dose insulin without close glucose monitoring.
  • Simultaneous infusion of hypertonic dextrose solutions exceeding recommended osmolarity.
  • Use with medications that cause severe hypoglycemia, such as sulfonylureas, without adjustment.

Use with caution

  • Concurrent IV fluids containing electrolytes; monitor serum sodium and potassium.
  • Patients receiving total parenteral nutrition; adjust carbohydrate contribution accordingly.
  • Individuals with renal impairment; assess fluid volume and glucose clearance.

Frequently Asked Questions

The primary component is glucose, anhydrous, which provides a sterile carbohydrate solution for intravenous use.

It is commonly used when rapid glucose delivery is needed, such as during surgery, in critical care, or when oral intake is not possible.

Glucosa Altan is classified as an excipient, specifically an intravenous solution that supplies glucose as a carbohydrate source.

Yes, it can be used in both pediatric and adult patients under the direction of a qualified healthcare professional.

Glucosa Altan is administered intravenously, typically through a sterile infusion set.

In most jurisdictions, including the EU, Glucosa Altan is available by prescription only and should be used under medical supervision.

Monitoring of blood glucose levels, fluid balance, and signs of electrolyte disturbances is recommended throughout the infusion.

Contraindications may include known hypersensitivity to glucose solutions and conditions where rapid fluid overload could be harmful.

The product should be stored according to the manufacturer’s instructions, typically in a cool, dry place protected from light until the expiration date.

It can serve as a diluent for compatible IV drugs, but compatibility should be verified before mixing.

Serious reactions may include severe hyperglycemia, allergic rash or hives, fluid overload leading to pulmonary edema, and significant electrolyte imbalances.

Yes, it may be incorporated into TPN formulations as the carbohydrate component, with adjustments made for total caloric needs.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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