Skip to content

Voriconazole

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

Voriconazole is a broad-spectrum triazole antifungal medication used to treat serious, potentially life-threatening fungal infections in patients with compromised immune systems. It is primarily prescribed for invasive aspergillosis, serious Candida infections, and other fungal infections that have not responded to other treatments.

Quick summary

A potent antifungal agent for treating serious invasive fungal infections in immunocompromised patients.

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

Key facts at a glance

ATC
J02AC03
RxNorm
121243
Generic
Voriconazole
Class
atc-j02
Brands
Vfend
Availability
rx
Lactation
unknown
Routes
oral
Forms
injection, suspension, tablet
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
400mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
200mg 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 exceeding 5 grams may cause serious toxicity
Chronic overdose: Prolonged use above recommended doses can lead to cumulative toxicity especially in patients with hepatic impairment
Immediate actions
Gastric lavage within 1-2 hours of ingestion, activated charcoal, supportive care, monitoring of liver function
Antidote
No specific antidote available(Treatment is supportive and symptomatic)
Poison Control: 1-800-222-1222

Special Populations

8 groups
✗

pregnancy

first trimester
unsafe
FDA Category
D
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks - known teratogenic effects

Monitor

regular fetal monitoring including ultrasound

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

⚠

pregnancy

second third trimester
caution
FDA Category
D
Dose Adjustment

use lowest effective dose

Key Recommendations

use only if benefits outweigh risks - consider alternative antifungals

Monitor

regular fetal monitoring

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
N
Dose Adjustment

discontinue breastfeeding

Key Recommendations

voriconazole is excreted in breast milk - breastfeeding not recommended

Monitor

none

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

✓

pediatric_age

children 2 11 years
safe
FDA Category
N
Dose Adjustment

weight-based dosing required

Key Recommendations

approved for use in children 2 years and older with invasive aspergillosis

Monitor

monitor liver function tests regularly

⚠

geriatric

elderly 65 years and older
caution
FDA Category
N
Dose Adjustment

no specific adjustment needed

Key Recommendations

use with caution due to potential decreased hepatic function

Monitor

monitor hepatic function and renal function

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

IV formulation contraindicated - use oral if needed

Key Recommendations

cyclodextrin vehicle accumulates in severe renal impairment - avoid IV formulation

Monitor

monitor renal function

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate
caution
FDA Category
N
Dose Adjustment

reduce maintenance dose by half

Key Recommendations

reduce dose to 200mg BID (from 200mg BID maintenance) for moderate hepatic impairment

Monitor

monitor liver function tests closely

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

severe
unsafe
FDA Category
N
Dose Adjustment

avoid use

Key Recommendations

not recommended for severe hepatic impairment - use alternative therapy

Monitor

not applicable

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

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2002

General prescribing information

drug_classWHO
2023

Drug class

Value:Azole antifungal

Drug class information

usageMedical guidelines
2023

Common uses

Value:Treatment of invasive aspergillosis, candidemia, esophageal candidiasis

Common therapeutic uses

pharmacologyFDA
2023

Mechanism of action

Value:Inhibition of fungal cytochrome P450 14α-demethylase

Pharmacological mechanism

Voriconazole is used to treat invasive aspergillosis (including fatal forms), candidemia in non-neutropenic patients, serious Candida infections (including resistant strains), and infections caused by Scedosporium and Fusarium species. It is typically reserved for serious infections when other antifungal therapies have failed or are inappropriate.

Voriconazole works by inhibiting the fungal cytochrome P450 enzyme 14α-demethylase, which is essential for converting lanosterol to ergosterol—a critical component of the fungal cell membrane. By disrupting ergosterol synthesis, the medication compromises the fungal cell membrane integrity, preventing fungal growth and replication.

Voriconazole carries significant risks including hepatotoxicity, visual disturbances (blurred vision, color changes), and severe drug interactions with many medications metabolized through CYP450 enzymes. It requires therapeutic drug monitoring to ensure adequate levels and reduce toxicity risk. Common side effects include visual disturbances, rash, nausea, vomiting, and headache. Use in pregnancy should be avoided due to potential fetal harm.

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

WellAlly may earn a referral fee from linked resources at no extra cost to you. Editorial content is never influenced by commercial relationships.

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