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Glycophos

Active Ingredient:
Sodium Glycerophosphate Pentahydrate
Origin:
EU

Glycophos (Sodium Glycerophosphate Pentahydrate)

Glycophos is a prescription‑only sodium glycerophosphate pentahydrate solution for injection, supplied in a sterile liquid form for intravenous administration. It provides inorganic phosphate to support cellular metabolism, bone mineralization, and electrolyte balance. Marketed in the European Union, Glycophos is used under medical supervision for conditions requiring phosphate supplementation.

Manufacturer / TM Owner

Fresenius Kabi Hellas Single Member S.A.

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Indications & Clinical Uses

Glycophos is indicated for clinical situations where phosphate replenishment is needed. It is commonly employed in the following contexts:

  • Treatment of hypophosphatemia in hospitalized patients.
  • Inclusion in parenteral nutrition regimens to meet phosphate requirements.
  • Electrolyte replacement during major surgery or critical illness.
  • Support of bone mineralization in patients with prolonged phosphate deficiency.
  • Adjunct therapy for metabolic disorders affecting phosphate metabolism.

Side Effects

Side effects of Glycophos vary in frequency and severity. They are generally related to the intravenous route and phosphate load.

Common

  • Mild injection site discomfort or erythema.
  • Transient nausea or vomiting.
  • Temporary elevation of serum calcium levels.
  • Mild headache.
  • Low-grade fever.

Serious

  • Hyperphosphatemia leading to calcium‑phosphate precipitation.
  • Acute renal failure in susceptible individuals.
  • Severe allergic reaction or anaphylaxis.
  • Cardiac arrhythmias due to electrolyte imbalance.
  • Metabolic acidosis in high‑dose scenarios.

Precautions & Warnings

When prescribing Glycophos, clinicians should consider several safety measures. Important precautions include:

  • Assess baseline serum phosphate, calcium, and renal function before initiation.
  • Adjust dose in patients with chronic kidney disease or impaired renal clearance.
  • Monitor electrolytes frequently during therapy to avoid hyperphosphatemia.
  • Use caution in patients with a history of hypersensitivity to phosphate preparations.
  • Avoid rapid infusion rates that may precipitate calcium‑phosphate complexes.
  • Discontinue if signs of severe allergic reaction develop.

Avoid Interactions

Glycophos may interact with other medications or clinical conditions. Interaction considerations are:

Avoid

  • Concurrent use of calcium supplements or calcium‑containing IV solutions without appropriate timing, due to risk of precipitation.
  • High‑dose vitamin D therapy that can increase calcium absorption.

Use with caution

  • Loop diuretics, which may alter calcium and phosphate balance.
  • Antacids containing aluminum or magnesium, which can affect phosphate absorption.
  • Blood‑pressure medications that influence renal perfusion.
  • Drugs that affect renal function, such as aminoglycosides.
  • Medications that prolong QT interval, as electrolyte shifts may exacerbate arrhythmias.

Frequently Asked Questions

Glycophos contains sodium glycerophosphate pentahydrate, which provides inorganic phosphate that participates in cellular energy production, bone mineralization, and maintenance of acid‑base balance.

Glycophos is prescribed for hypophosphatemia, as part of parenteral nutrition, and for general electrolyte replacement in patients who cannot receive oral phosphate.

Glycophos is supplied as a sterile solution for intravenous injection and is administered by a healthcare professional under controlled infusion rates.

Baseline serum phosphate, calcium, creatinine, and overall renal function should be measured to determine appropriate dosing and monitor safety.

Yes, but dosing must be adjusted and serum electrolytes closely monitored because reduced renal clearance can increase the risk of hyperphosphatemia.

Common side effects include mild injection site irritation, transient nausea, headache, low‑grade fever, and temporary changes in calcium levels.

Serious reactions include hyperphosphatemia, acute renal failure, severe allergic reactions such as anaphylaxis, cardiac arrhythmias, and metabolic acidosis.

Calcium-containing products should be administered separately and timed to avoid simultaneous infusion, as they can precipitate with phosphate.

Electrolytes are typically checked daily or more frequently if the patient has renal impairment or is receiving high‑dose phosphate.

Glycophos is a prescription‑only medication and must be ordered by a licensed healthcare provider.

Patients with known hypersensitivity to phosphate preparations should be evaluated carefully, and infusion should be stopped immediately if an allergic reaction occurs.

The safety of Glycophos in pregnancy has not been established; it should be used only if the potential benefit justifies the potential risk to the fetus.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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