What is the maximum recommended dosage of fosphenytoin (antiepileptic medication)?

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Maximum Dosage of Fosphenytoin

The maximum infusion rate for fosphenytoin is 150 mg PE/min in adults and 2 mg PE/kg/min (or 150 mg PE/min, whichever is slower) in pediatric patients. 1

Dosing Guidelines for Fosphenytoin

Status Epilepticus (Emergency Dosing)

  • Adults: 15-20 mg PE/kg at a rate of 100-150 mg PE/min, not exceeding 150 mg PE/min 2, 1
  • Pediatric patients: 15-20 mg PE/kg at a rate of 1-3 mg PE/kg/min (maximum rate: 150 mg PE/min or 2 mg PE/kg/min, whichever is slower) 2, 1

Non-Emergent Loading and Maintenance Dosing

  • Adults:

    • Loading dose: 10-20 mg PE/kg at a rate not exceeding 150 mg PE/min 3, 1
    • Maintenance dose: 4-6 mg PE/kg/day in divided doses 1
  • Pediatric patients:

    • Loading dose: 10-15 mg PE/kg at a rate of 1-2 mg PE/kg/min (or 150 mg PE/min, whichever is slower) 1
    • Initial maintenance dose: 2-4 mg PE/kg given 12 hours after loading dose 1
    • Subsequent maintenance doses: 4-8 mg PE/kg/day in divided doses 1

Important Administration Considerations

Route of Administration

  • Intravenous (IV) administration is preferred for status epilepticus 1
  • Intramuscular (IM) administration should ordinarily not be used in status epilepticus or in pediatric patients 1

Preparation and Dilution

  • Dilute in 5% Dextrose Injection or 0.9% Sodium Chloride Injection 1
  • Concentration should range from 1.5 to 25 mg PE/mL 1
  • Maximum concentration should not exceed 25 mg PE/mL 1

Safety Precautions

  • Continuous monitoring of ECG, blood pressure, and respiratory function is essential during administration 1
  • Observe patients throughout the period where maximal serum phenytoin concentrations occur (approximately 10-20 minutes after the end of infusion) 1
  • Monitor heart rate via ECG and reduce infusion rate if heart rate decreases by 10 beats per minute 2
  • When given IV, itching is common and can be controlled by reducing the flow rate 2

Common Pitfalls and Caveats

  1. Medication errors: Fatal overdoses have occurred when the concentration of the vial (50 mg PE/mL) was misinterpreted to mean that the total content of the vial was 50 mg PE. Always ensure the appropriate volume is withdrawn from the vial 1

  2. Cardiovascular risks: Exceeding the maximum infusion rate can cause cardiac arrhythmias and hypotension 3

  3. Compatibility issues: Fosphenytoin should be diluted in normal saline only, as it is incompatible with glucose-containing solutions 3

  4. Therapeutic monitoring: After fosphenytoin administration, phenytoin concentrations should not be monitored until conversion to phenytoin is essentially complete (approximately 2 hours after IV infusion) 1

  5. Target therapeutic concentrations: Aim for serum total phenytoin concentrations of 10-20 mcg/mL (unbound phenytoin concentrations of 1-2 mcg/mL) 1

Fosphenytoin offers advantages over phenytoin due to its greater aqueous solubility, resulting in fewer adverse effects and less soft-tissue injury 4. It can be administered more rapidly than phenytoin, allowing for quicker achievement of therapeutic levels in emergency situations 5.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Medication Administration and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Safety of fosphenytoin sodium.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 1996

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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