To become available it is necessary for the phosphate group to be hydrolysed from the glycerophosphate molecule. The hydrolysis occurs maximally at a plasma concentration of >0.7 mmol/l. Assuming that all hydrolysis of glycerophosphate takes place in plasma, about 12-15 mmol of sodium glycerophosphate will be hydrolysed each day in individuals with normal serum alkaline phosphatase.
No pharmacokinetical data is available for infants, however with the recommended dosage hyperphosphataemia is unlikely.
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| Hypophosphataemia |
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GFR ≥10 ml/min/1.73m2: Dose adjustment not required.
GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Hypernatraemia, hyperphosphataemia, shock or dehydration.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Glycophos should be used with caution in patients with impaired renal function. The phosphate status of all patients should be monitored regularly. Be aware that glycophos contains sodium.
Glycophos must not be given undiluted.
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The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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| Electrolyte solutions | ||
|---|---|---|
| B05XA07 | ||
| B05XA19 | ||
| B05XA31 | ||
| B05XA06 | ||
| Amino acids | ||
|---|---|---|
| B05XB01 | ||
| Vitamins | ||
|---|---|---|
| B05XC | ||
| VITAMINS | ||
|---|---|---|
| B05XC | ||
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