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Glycophos

Active Ingredient:
Sodium Glycerophosphate Pentahydrate
Origin:
EU

Glycophos (Sodium Glycerophosphate Pentahydrate)

Glycophos is a sodium glycerophosphate pentahydrate solution for injection, supplied as a sterile intravenous preparation. It contains the active ingredient sodium glycerophosphate pentahydrate and is marketed in the European Union as a prescription‑only electrolyte supplement. The product is used to replenish phosphate and sodium levels in patients requiring intravenous phosphate replacement. Glycophos is administered by healthcare professionals under controlled conditions and is stored according to manufacturer guidelines to maintain stability.

Manufacturer / TM Owner

Fresenius Kabi Ab

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Indications & Clinical Uses

Glycophos is indicated for clinical situations where phosphate repletion is required through the intravenous route.

  • Treatment of hypophosphatemia associated with critical illness, surgery, or renal replacement therapy.
  • Supplementation of phosphate in patients receiving total parenteral nutrition (TPN) who have limited oral intake.
  • Electrolyte replacement in patients with phosphate depletion due to prolonged fasting, severe burns, or extensive trauma.
  • Support of metabolic processes that depend on phosphate, such as ATP synthesis and cellular signaling.
  • Adjunctive therapy during dialysis or continuous renal replacement therapy when phosphate losses are anticipated.

Side Effects

Adverse reactions to Glycophos are generally related to the infusion of phosphate and sodium and may vary in frequency and severity.

Common

  • Transient hyperphosphatemia leading to mild serum phosphate elevation.
  • Temporary hypernatremia causing mild increase in serum sodium.
  • Local irritation or pain at the injection site.
  • Mild gastrointestinal discomfort such as nausea.

Serious

  • Severe hyperphosphatemia that may precipitate calcium‑phosphate deposition in tissues.
  • Acute metabolic alkalosis resulting from rapid sodium load.

Precautions & Warnings

When prescribing Glycophos, clinicians should evaluate patient-specific factors and monitor laboratory values to minimize risks.

  • Assess baseline serum phosphate, calcium, and sodium levels before initiating therapy.
  • Adjust dose in patients with renal impairment or reduced glomerular filtration rate.
  • Avoid rapid infusion rates to prevent sudden shifts in electrolyte balance.
  • Monitor cardiac rhythm in patients with existing electrolyte abnormalities.
  • Use caution in individuals with a history of hypercalcemia or metastatic calcification.
  • Discontinue or reduce infusion if serum phosphate exceeds the therapeutic target.

Avoid Interactions

Glycophos may interact with other medications that influence electrolyte balance or renal function, requiring careful management.

Avoid

  • Concomitant administration of calcium‑containing solutions that can precipitate calcium‑phosphate complexes.
  • High‑dose vitamin D analogues that increase intestinal phosphate absorption.

Use with caution

  • Loop diuretics, which may enhance renal phosphate loss and alter serum levels.
  • ACE inhibitors or ARBs, which can affect renal handling of electrolytes.
  • Parenteral nutrition formulations containing phosphate, to avoid cumulative excess.

Frequently Asked Questions

The active ingredient in Glycophos is sodium glycerophosphate pentahydrate.

Glycophos is supplied as a sterile solution for injection and is administered intravenously by a healthcare professional.

Glycophos is used for hypophosphatemia, phosphate depletion during parenteral nutrition, and general electrolyte replacement therapy.

Dose adjustment and careful monitoring are recommended for patients with renal impairment because reduced kidney function can affect phosphate clearance.

Baseline serum phosphate, calcium, and sodium levels should be measured prior to initiating Glycophos therapy.

Common side effects include transient hyperphosphatemia, temporary hypernatremia, local injection‑site irritation, and mild nausea.

Serious events may include severe hyperphosphatemia leading to calcium‑phosphate precipitation and acute metabolic alkalosis from rapid sodium administration.

Mixing Glycophos with calcium‑containing solutions should be avoided because it can cause calcium‑phosphate precipitation.

The pregnancy safety category for Glycophos is listed as unknown; it should only be used if the potential benefit justifies the potential risk to the fetus.

Serum phosphate should be monitored regularly, typically every 4–6 hours initially, and then adjusted based on clinical response and target levels.

Glycophos is a prescription product; pediatric use should be determined by a physician based on weight‑based dosing and clinical need.

Glycophos should be stored according to the manufacturer’s instructions, usually in a controlled temperature environment away from light and moisture.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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