Product image of Glucohalal (Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Glucose) supplied by GNH India

Glucohalal

Active Ingredient:
Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Glucose
Origin:
EU

Glucohalal (Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Glucose)

Glucohalal is an oral preparation containing sodium hydrogen carbonate, potassium chloride, sodium chloride, and glucose. The product is marketed in the European Union, though specific strength and dosage form are not disclosed. It is presented without a brand name and is classified as a pharmaceutical compound with unknown therapeutic class. Glucohalal is intended for use under professional supervision, and its composition suggests potential roles in electrolyte and glucose supplementation.

Manufacturer / TM Owner

Northumbria Pharma Limited

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Indications & Clinical Uses

Glucohalal is formulated with electrolyte salts and glucose, which may be considered in clinical situations that require supplementation of these components.

  • Oral electrolyte replacement in mild dehydration.
  • Adjunctive glucose source for patients with low blood sugar under supervision.
  • Supportive care during gastrointestinal losses.
  • Temporary supplementation during fasting or pre‑operative preparation.

Side Effects

The safety profile of Glucohalal reflects the known effects of its individual ingredients.

Common

  • Mild gastrointestinal discomfort such as nausea or bloating.
  • Transient increase in urinary output.
  • Slight alteration in taste perception.

Serious

  • Hypernatremia or hyperkalemia in patients with impaired renal function.
  • Severe electrolyte imbalance leading to cardiac arrhythmia.
  • Allergic reaction including rash, itching, or swelling.

Precautions & Warnings

When considering Glucohalal, several precautionary measures should be observed to minimize risk.

  • Assess renal and cardiac function before initiating therapy.
  • Monitor serum electrolytes regularly during use.
  • Avoid in individuals with known hypersensitivity to any component.
  • Use with caution in patients taking diuretics or antihypertensive agents.
  • Do not exceed the recommended volume without medical guidance.
  • Keep the product out of reach of children.

Avoid Interactions

Glucohalal may interact with other medications or substances that affect electrolyte balance or glucose metabolism.

Avoid

  • Concurrent use with high‑dose potassium supplements.
  • Combination with sodium‑rich intravenous fluids.
  • Co‑administration with medications that prolong the QT interval.

Use with caution

  • Diuretics that alter sodium or potassium levels.
  • ACE inhibitors or ARBs that affect potassium homeostasis.
  • Insulin or oral hypoglycemic agents due to added glucose.
  • Antacids containing sodium bicarbonate.

Frequently Asked Questions

Glucohalal includes sodium hydrogen carbonate, potassium chloride, sodium chloride, and glucose as its listed active components.

The product is intended for oral administration, typically as a liquid or dissolved preparation, depending on the specific dosage form supplied.

Glucohalal may be considered when electrolyte replenishment or supplemental glucose is needed, such as mild dehydration, gastrointestinal fluid loss, or pre‑operative fasting.

It can be used as part of an oral rehydration strategy to replace sodium, potassium, and glucose losses, but clinical judgment is required to determine suitability.

Common side effects may include mild gastrointestinal discomfort, increased urinary output, and a temporary change in taste.

Serious reactions can involve electrolyte disturbances such as hypernatremia or hyperkalemia, cardiac arrhythmias, and allergic responses like rash or swelling.

Patients with known hypersensitivity to any ingredient, severe renal impairment, or uncontrolled cardiac conditions should avoid using Glucohalal without medical advice.

Serum sodium and potassium concentrations should be checked periodically, especially in patients with renal disease or those receiving other electrolyte‑affecting drugs.

Yes, diuretics can alter sodium and potassium balance, so concurrent use should be approached with caution and electrolyte monitoring.

The regulatory status of Glucohalal in the EU is not clearly defined; it may require a prescription depending on national regulations.

Safety information for pregnancy and lactation has not been established; healthcare providers should evaluate risks and benefits before use.

Store the product at room temperature, protected from moisture and direct sunlight, and keep it out of reach of children.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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