Product image of Glucothera (Sodium Lactate Solution, Magnesium Chloride Hexahydrate, Sodium Chloride, Calcium Chloride Dihydrate) supplied by GNH India

Glucothera

Active Ingredient:
Sodium Lactate Solution, Magnesium Chloride Hexahydrate, Sodium Chloride, Calcium Chloride Dihydrate
Origin:
EU

Glucothera (Sodium Lactate Solution, Magnesium Chloride Hexahydrate, Sodium Chloride, Calcium Chloride Dihydrate)

Glucothera is an injectable electrolyte solution containing sodium lactate, magnesium chloride, sodium chloride, and calcium chloride. The formulation is supplied as a sterile solution for injection, with the specific concentration not disclosed. Designed for use in clinical settings, Glucothera provides a source of key electrolytes and fluid volume to help maintain plasma osmolarity and electrolyte balance. It is marketed in the European Union pharmaceutical market.

Manufacturer / TM Owner

Iperboreal Pharma S.R.L.

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Indications & Clinical Uses

Glucothera is indicated for clinical situations that require rapid fluid and electrolyte replacement, particularly when patients are unable to maintain adequate intravascular volume through oral intake.

  • Fluid resuscitation in hypovolemic patients to quickly restore circulating blood volume.
  • Electrolyte replacement for metabolic disturbances such as hyponatremia or hypomagnesemia.
  • Support of parenteral nutrition regimens by providing essential sodium, calcium, and magnesium ions.
  • Management of postoperative fluid losses through continuous infusion to maintain hemodynamic stability.
  • Treatment of dehydration due to gastrointestinal losses, including vomiting or diarrhea, with balanced electrolyte composition.
  • Use during dialysis to replenish electrolytes lost during the treatment process.

Side Effects

Adverse reactions to Glucothera are generally related to its electrolyte composition and route of administration.

Common

  • Injection site pain, erythema, or mild swelling.
  • Transient increase in serum sodium concentration.
  • Mild metabolic alkalosis due to lactate metabolism.
  • Slight elevation of serum magnesium levels without clinical symptoms.

Serious

  • Severe electrolyte imbalance such as hypernatremia, hypermagnesemia, or hypercalcemia.
  • Anaphylactic or severe hypersensitivity reaction.
  • Cardiac arrhythmias caused by rapid shifts in electrolyte concentrations.
  • Pulmonary edema or fluid overload in patients with compromised cardiac function.

Precautions & Warnings

When using Glucothera, clinicians should consider several safety factors to minimize risk.

  • Obtain baseline serum electrolyte and renal function tests before initiating therapy.
  • Monitor serum electrolytes and fluid balance regularly during infusion.
  • Adjust infusion rate in patients with cardiac or renal impairment to avoid overload.
  • Avoid administration in individuals with known hypersensitivity to any component of the solution.
  • Use caution in pregnant or lactating women until safety data are available.
  • Evaluate total fluid input to prevent pulmonary edema in at‑risk patients.
  • Ensure compatibility with the infusion set and avoid mixing with incompatible solutions.

Avoid Interactions

Glucothera may interact with other agents that affect electrolyte balance or fluid status.

Avoid

  • Concurrent infusion of high‑dose sodium bicarbonate solutions.
  • Co‑administration with calcium‑containing parenterals without compatibility testing.
  • Simultaneous use of hypertonic saline solutions.

Use with caution

  • Concomitant use of loop or thiazide diuretics.
  • Concurrent therapy with ACE inhibitors, ARBs, or other renin‑angiotensin system blockers.
  • Administration alongside cardiac glycosides such as digoxin.

Frequently Asked Questions

Glucothera contains sodium lactate, magnesium chloride hexahydrate, sodium chloride, and calcium chloride dihydrate in a sterile aqueous solution for injection.

Glucothera is supplied as a solution for injection and is typically administered via the intraperitoneal route under controlled medical supervision.

It is used for fluid resuscitation, electrolyte replacement, support of parenteral nutrition, postoperative fluid management, treatment of dehydration, and during dialysis to restore electrolyte balance.

Baseline and periodic assessment of serum electrolytes, renal function, and fluid balance is recommended, along with observation for signs of overload or adverse reactions.

Use in children should be based on clinical judgment, with dosing and monitoring adjusted for age, weight, and underlying medical conditions.

Common effects include injection‑site discomfort, transient increases in serum sodium, mild metabolic alkalosis, and slight elevations in magnesium levels.

Unlike normal saline, Glucothera provides multiple electrolytes (sodium, magnesium, calcium) and lactate, offering a broader electrolyte profile for specific replacement needs.

Compatibility should be verified for each co‑administered drug; avoid mixing with calcium‑containing solutions or hypertonic saline without proper testing.

Renal function should be evaluated before use, infusion rates may need reduction, and electrolyte levels must be closely monitored to prevent accumulation.

Store the unopened vials in a controlled room temperature environment, protected from light, and discard any solution that appears discolored or particulate.

Safety data in pregnancy are limited; it should be used only if the potential benefit justifies the potential risk to the fetus.

Glucothera supplies sodium, magnesium, calcium, and lactate, which together help re‑establish plasma osmolarity and replenish depleted electrolytes, supporting normal cellular function.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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