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Fosphenytoin

Published: July 26, 2026Updated: July 26, 2026

Fosphenytoin is an anticonvulsant medication used to treat and prevent certain types of seizures, including status epilepticus. It is a water-soluble prodrug that is converted in the body to phenytoin, allowing for intravenous or intramuscular administration when rapid seizure control is needed. This medication is typically used in hospital settings for patients who cannot take oral antiepileptic drugs.

Quick summary

Fosphenytoin is an injectable anticonvulsant prodrug of phenytoin used to treat and prevent seizures, particularly in emergency and hospital settings.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy
BOXED WARNING

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
N03AB05
RxNorm
72236
Generic
Fosphenytoin
Class
atc-n03
Brands
Cerebyx
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose of approximately 10,000 mg or more of fosphenytoin sodium may cause serious toxicity
Chronic overdose: Chronic toxicity can occur with sustained supratherapeutic levels exceeding 30 mcg/mL; cumulative dosing above recommended limits may lead to toxicity
Immediate actions
Supportive care, airway management, activated charcoal if within 1-2 hours of ingestion, intravenous fluids, cardiac monitoring
Antidote
No specific antidote exists for fosphenytoin overdose(Treatment is supportive; effectiveness depends on timely intervention and severity of overdose)
Poison Control: 1-800-222-1222

Special Populations

7 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; consider alternative antiseizure medications with better safety profile

Monitor

regular fetal monitoring including ultrasound for fetal growth

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

pregnancy

second third trimester
caution
FDA Category
C
Dose Adjustment

monitor levels closely

Key Recommendations

maintain therapeutic phenytoin levels; dose adjustments often needed as pregnancy progresses due to altered pharmacokinetics

Monitor

frequent phenytoin plasma level monitoring; fetal growth monitoring

Use with caution and monitor for adverse effects.

✗

lactation

none
unsafe
FDA Category
N
Dose Adjustment

avoid or discontinue breastfeeding

Key Recommendations

fosphenytoin and its metabolite phenytoin pass into breast milk; breastfeeding not recommended

Monitor

monitor infant for signs of phenytoin exposure including sedation, feeding difficulties

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

geriatric

none
caution
FDA Category
N
Dose Adjustment

reduce initial dose

Key Recommendations

start at lower end of dosing range; reduced hepatic metabolism and protein binding in elderly

Monitor

monitor phenytoin levels and for signs of toxicity including ataxia, dizziness, nystagmus

Use with caution and monitor for adverse effects.

⚠

pediatric_age

neonates infants
caution
FDA Category
N
Dose Adjustment

weight-based dosing with careful titration

Key Recommendations

approved for use in pediatric patients including neonates; doses expressed as phenytoin equivalents (PE)

Monitor

closely monitor phenytoin levels; monitor for cardiac effects especially IV administration

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

may require dose reduction

Key Recommendations

fosphenytoin is metabolized to phenytoin which is highly protein bound; in renal impairment, monitor free phenytoin levels

Monitor

monitor both total and free phenytoin levels; watch for toxicity

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

significant dose reduction required

Key Recommendations

fosphenytoin is metabolized in liver to phenytoin; hepatic impairment reduces metabolism

Monitor

frequent phenytoin level monitoring; monitor liver function tests

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

Commonly prescribed since

Value:1996

FDA approval year for intravenous use

Drug classWHO
2023

Anticonvulsant

Value:Anticonvulsant/Antiepileptic

ATC classification N03AB12 - phenytoin derivatives

usageMedical guidelines
2023

Common uses

Value:Status epilepticus, seizure control

Primary therapeutic indications

administrationFDA
2023

Route of administration

Value:Intravenous, Intramuscular

Available formulations

Treatment and prevention of generalized tonic-clonic seizures, complex partial seizures, and status epilepticus. Primarily used in acute care settings when rapid IV or IM administration is required.

Fosphenytoin is a prodrug that is converted to phenytoin in the bloodstream. Its anticonvulsant effects are achieved through voltage-dependent blockade of sodium channels in neurons, which stabilizes neuronal membranes and prevents the spread of seizure activity.

Must be administered slowly via IV (no faster than 150 mg PE/minute) due to risk of severe cardiovascular reactions including hypotension and arrhythmias. Requires cardiac monitoring during infusion. May cause drowsiness, dizziness, or coordination problems. Cross-reacts with phenytoin in serum drug testing.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed July 26, 2026. · Read our editorial policy