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Glycerophosphate De Sodium

Active Ingredient:
Sodium Glycerophosphate Pentahydrate
Origin:
EU

Glycerophosphate De Sodium (Sodium Glycerophosphate Pentahydrate)

Glycerophosphate De Sodium is a sterile aqueous solution for injection that contains sodium glycerophosphate pentahydrate as its active ingredient. It is supplied in a standard concentration for intravenous use and is marketed in the European Union. The product provides a readily bioavailable source of phosphate for patients requiring parenteral nutrition. Each vial typically contains 0.5 g of the pentahydrate dissolved in 100 mL of isotonic solution, allowing precise dosing in clinical settings.

Manufacturer / TM Owner

Fresenius Kabi France S.A.S.

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Indications & Clinical Uses

Glycerophosphate De Sodium is primarily used to supplement phosphate in patients receiving parenteral nutrition when oral intake is insufficient or contraindicated.

  • Provides inorganic phosphate for cellular metabolism and bone mineralization.
  • Supports energy production through ATP synthesis in critically ill patients.
  • Helps maintain acid‑base balance by acting as a buffer in intravenous solutions.
  • Used in neonatal and pediatric intensive care where phosphate requirements are high.
  • Can be incorporated into customized total parenteral nutrition (TPN) admixtures.
  • Facilitates renal phosphate reabsorption when administered with appropriate electrolyte balance.

Side Effects

Adverse reactions to Glycerophosphate De Sodium are generally infrequent, but they may occur depending on patient condition and infusion rate.

Common

  • Mild transient hyperphosphatemia that resolves after infusion.
  • Local irritation at the injection site, such as pain or erythema.
  • Nausea or mild gastrointestinal discomfort when administered rapidly.
  • Transient increase in serum calcium due to complex formation.

Serious

  • Severe hyperphosphatemia leading to calcium‑phosphate precipitation and possible renal dysfunction.
  • Hypocalcemia secondary to rapid phosphate shift.
  • Allergic reactions ranging from urticaria to anaphylaxis.
  • Metabolic acidosis if large volumes are infused without appropriate buffering.
  • Cardiovascular instability such as hypotension or arrhythmia in patients with severe electrolyte disturbances.

Precautions & Warnings

When using Glycerophosphate De Sodium, clinicians should observe specific precautions to minimize risks and ensure safe phosphate supplementation.

  • Assess baseline serum phosphate, calcium, and renal function before initiation.
  • Adjust dose in patients with impaired renal clearance to avoid accumulation.
  • Monitor serum electrolytes regularly during therapy, especially calcium and phosphate levels.
  • Use caution in patients with hyperparathyroidism or active bone disease.
  • Avoid rapid infusion rates that may provoke sudden shifts in serum phosphate.
  • Consider compatibility with other intravenous solutions to prevent precipitation.

Avoid Interactions

Glycerophosphate De Sodium may interact with certain intravenous medications or solutions, influencing electrolyte balance or causing precipitation.

Avoid

  • Co‑administration with calcium‑containing solutions without proper mixing protocols, which can precipitate calcium phosphate.
  • Simultaneous infusion with high‑dose vitamin D analogues that increase calcium absorption, raising risk of hypercalcemia.
  • Avoid mixing with alkaline solutions that may raise pH and promote precipitation.

Use with caution

  • Concurrent use of loop diuretics, as they can alter renal phosphate handling.
  • Administration alongside parenteral nutrition containing magnesium, requiring electrolyte monitoring.
  • Use with beta‑agonists that may shift intracellular phosphate.
  • Monitor cardiac function when combined with drugs that affect calcium signaling, such as digitalis.

Frequently Asked Questions

Glycerophosphate De Sodium supplies inorganic phosphate, an essential electrolyte, to patients receiving total parenteral nutrition (TPN) when oral or enteral intake is not possible.

It is administered as a sterile solution for injection, typically infused intravenously over a controlled period according to the prescribed rate and patient needs.

Serum phosphate, calcium, magnesium, and renal function (creatinine, eGFR) should be monitored regularly to detect electrolyte shifts or accumulation.

Mixing with calcium‑containing solutions can cause calcium‑phosphate precipitation; it should be avoided unless compatibility is confirmed by proper mixing protocols.

Signs may include muscle cramps, itching, joint pain, and in severe cases, calcium‑phosphate deposition leading to renal dysfunction or cardiovascular complications.

It can be used in neonatal intensive care when phosphate supplementation is required, but dosing and monitoring must be carefully adjusted for the infant's size and renal function.

Renal impairment reduces phosphate clearance; therefore, the dose should be reduced and serum phosphate levels monitored closely to avoid accumulation.

A common formulation contains 0.5 g of sodium glycerophosphate pentahydrate per 100 mL of isotonic solution, though exact concentrations may vary by manufacturer.

Contraindications include known hypersensitivity to the product and conditions where phosphate administration could exacerbate calcium‑phosphate precipitation, such as severe hypercalcemia.

Loop diuretics increase urinary phosphate excretion; when used together, clinicians should monitor serum phosphate to ensure adequate supplementation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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