Product image of Glucosio Con Potassio Cloruro Ii Bioindustria L.I.M. (Potassium Chloride, Glucose Monohydrate) supplied by GNH India

Glucosio Con Potassio Cloruro Ii Bioindustria L.I.M.

Active Ingredient:
Potassium Chloride, Glucose Monohydrate
Origin:
EU

Glucosio Con Potassio Cloruro Ii Bioindustria L.I.M. (Potassium Chloride, Glucose Monohydrate)

Glucosio Con Potassio Cloruro Ii, marketed by Bioindustria L.I.M., is an injectable solution that combines potassium chloride and glucose monohydrate in a single formulation; the exact strength is not disclosed on the label. Designed for intravenous administration, this prescription‑only product is intended for use in clinical settings within the European Union. It functions as an electrolyte supplement and glucose source to support fluid and electrolyte therapy.

Manufacturer / TM Owner

Bioindustria Lim Laboratorio Italiano Medicinali Spa

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Indications & Clinical Uses

Glucosio Con Potassio Cloruro Ii is indicated for several clinical situations where potassium and energy replenishment are required.

  • Treatment of hypokalemia or potassium depletion in hospitalized patients.
  • Fluid replacement therapy during postoperative recovery or acute illness.
  • Prevention of electrolyte imbalance in patients undergoing major surgery.
  • Support of intracellular fluid shifts when combined with other IV fluids.
  • Adjunctive therapy for patients receiving insulin to mitigate hypoglycemia‑induced potassium shifts.
  • Correction of potassium loss associated with diuretic therapy in critical‑care settings.

Side Effects

Side‑effect profiles for Glucosio Con Potassio Cloruro Ii reflect the pharmacologic actions of potassium chloride and glucose when administered intravenously. These events are generally dose‑dependent and monitored during therapy, occasionally requiring adjustment.

Common

  • Mild transient hyperglycemia due to glucose infusion.
  • Local irritation or pain at the injection site.
  • Slight increase in serum potassium that may cause mild muscle weakness.
  • Nausea or vomiting related to rapid glucose administration.

Serious

  • Severe hyperkalemia leading to cardiac arrhythmias.
  • Hyperosmolar hyperglycemic state in patients with impaired glucose tolerance.
  • Allergic or anaphylactic reaction to the formulation components.
  • Metabolic acidosis secondary to rapid potassium infusion in patients with renal impairment.

Precautions & Warnings

When prescribing Glucosio Con Potassio Cloruro Ii, clinicians should evaluate patient‑specific factors to minimize risks associated with potassium and glucose administration.

  • Verify baseline serum potassium and glucose levels before infusion.
  • Adjust dose in patients with renal insufficiency or on dialysis.
  • Use caution in individuals with cardiac disease or arrhythmias.
  • Avoid rapid infusion rates to reduce the risk of hyperkalemia.
  • Monitor cardiac rhythm and blood pressure during and after administration.
  • Consider alternative fluid therapy for patients with known hypersensitivity to formulation excipients.

Avoid Interactions

Glucosio Con Potassio Cloruro Ii may interact with other medications that affect potassium balance, glucose metabolism, or cardiac conduction.

Avoid

  • Concurrent use with potassium‑sparing diuretics or ACE inhibitors without electrolyte monitoring.
  • Co‑administration with rapid‑acting insulin boluses in uncontrolled diabetes.
  • Avoid simultaneous infusion with calcium gluconate solutions, as they may precipitate potassium chloride.

Use with caution

  • Combine with other IV fluids containing potassium; adjust total potassium load.
  • Use alongside beta‑adrenergic agonists, which can shift potassium intracellularly.
  • Administer with nephrotoxic drugs; monitor renal function closely.
  • Give together with medications that prolong QT interval; observe ECG changes.

Frequently Asked Questions

It provides potassium ions and glucose intravenously to correct potassium deficiency and supply energy during fluid and electrolyte therapy.

It is used for hypokalemia, potassium depletion, postoperative fluid replacement, prevention of electrolyte imbalance during surgery, and as an adjunct when insulin therapy may shift potassium.

The product is supplied as an injection solution for intravenous (IV) infusion under medical supervision.

Yes, it is classified as a prescription‑only (Rx) product in the European Union.

Baseline serum potassium and glucose levels should be measured to guide dosing and monitor safety.

Patients with renal impairment may require dose adjustment and close monitoring of potassium and fluid status.

Common effects include mild transient hyperglycemia, local injection‑site irritation, mild muscle weakness from potassium rise, and occasional nausea or vomiting.

Serious reactions can include severe hyperkalemia with cardiac arrhythmias, hyperosmolar hyperglycemic state, allergic or anaphylactic responses, and metabolic acidosis in renal‑compromised patients.

Yes, rapid infusion can increase the risk of hyperkalemia; infusion rates should follow institutional protocols and patient tolerance.

Concurrent use with potassium‑sparing diuretics, ACE inhibitors, or calcium gluconate solutions without monitoring should be avoided.

It may be used as an adjunct to insulin to prevent hypoglycemia‑induced potassium shifts, but glucose and potassium levels must be closely monitored.

Continuous cardiac monitoring, periodic serum potassium and glucose checks, and blood pressure observation are recommended throughout the infusion.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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