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Voriconazole (Vfend)

Raw research findings for this medication. Mostly single studies, not curated or confirmed robust.

About Voriconazole

What it is

Voriconazole is an azole antifungal: it blocks the fungal enzyme that makes ergosterol, a building block of the fungal cell membrane. It is used for serious fungal infections such as invasive aspergillosis and some Candida infections, often in people whose immune system is weakened. It is sold as Vfend, among other names.

How genes come into it

Voriconazole is broken down mainly by the liver enzyme CYP2C19, and its blood levels vary widely between people. Poor metabolizers keep much more of it, with a higher chance of side effects such as visual disturbances and liver effects; people with the fast *17 version on both copies (ultrarapid metabolizers) may clear it too quickly for it to reach working levels. CPIC and DPWG have published guidelines on CYP2C19 and voriconazole, and the US FDA lists it as affecting safety. Studies have also looked at CYP3A4 and other genes, with weaker evidence.

Published guidelines

Clinical guidelines that name a gene for Voriconazole. They sort people into groups by the gene copies they carry.

CPIC guideline: CYP2C19. Ultrarapid Metabolizer · Rapid Metabolizer · Normal Metabolizer · Likely Intermediate Metabolizer · Intermediate Metabolizer · Likely Poor Metabolizer · Poor Metabolizer · Indeterminate. Strong. 2017.

DPWG guideline: CYP2C19. Ultrarapid Metabolizer · Rapid Metabolizer · Normal Metabolizer · Likely Intermediate Metabolizer · Intermediate Metabolizer · Likely Poor Metabolizer · Poor Metabolizer · Indeterminate. 2011.

US FDA: CYP2C19. Likely Intermediate Metabolizer · Intermediate Metabolizer · Likely Poor Metabolizer · Poor Metabolizer. Data that Indicate a Potential Impact on Safety or Response.

What research found

Every published finding on gene variants and Voriconazole. Upload your DNA file to see which of these rows apply to you.

Rated evidence (4 rated variants)

PharmGKB weighs all studies of a variant and rates how strong the evidence is, from 1A (strongest) to 4.

CYP2C19 CYP2C19*1, CYP2C19*2, CYP2C19*3, CYP2C19*17: Level 1A · replicated. Metabolism/PK. 47.

SLCO2B1 rs3781727: Level 3. Metabolism/PK. 1.

CYP3A4 rs4646437: Level 3. Metabolism/PK: Fungal infectious disease. 1.

ABCB1 rs1045642: Level 3. Metabolism/PK. 1.

Metabolism (109 findings)

Studies of how quickly the body processes this medication.

ABCB1 rs1045642: Genotype AA is associated with decreased metabolism of voriconazole in healthy individuals as compared to genotype GG.

ABCB1 rs1045642: Genotype AA is associated with decreased trough concentration of voriconazole in children as compared to genotypes AG + GG.

ABCC2 rs717620: Genotypes CT + TT is associated with increased trough concentration of voriconazole in children as compared to genotype CC.

ABCG2 rs13120400: Genotype CC is associated with increased trough concentration of voriconazole in children as compared to genotypes CT + TT.

Response (5 findings)

Studies of how well it worked in people carrying a variant.

CYP2C19 CYP2C19 poor metabolizer and intermediate metabolizer genotypes: CYP2C19 intermediate metabolizer and poor metabolizer is associated with increased clinical benefit to voriconazole as compared to CYP2C19 normal metabolizer.

CYP2C19 CYP2C19 poor metabolizers: CYP2C19 poor metabolizer is associated with increased response to voriconazole as compared to CYP2C19 normal metabolizer.

CYP2C19 CYP2C19*1, CYP2C19*17: CYP2C19 *1/*17 is associated with decreased response to voriconazole in people with Mycoses.

CYP2C19 CYP2C19*17: CYP2C19 *17/*17 is associated with decreased response to voriconazole in women with Mycoses.

Dosing (11 findings)

Studies of how much of the drug people needed or tolerated.

CYP2C19 CYP2C19*1, CYP2C19*17: CYP2C19 *17/*17 (assigned as ultrarapid metabolizer phenotype) is associated with decreased dose-adjusted trough concentrations of voriconazole in children with Neoplasms as compared to CYP2C19 *1/*1 (assigned as normal metabolizer phenotype) .

CYP2C19 CYP2C19*1, CYP2C19*17: CYP2C19 *1/*17 + *17/*17 is associated with increased dose of voriconazole in people with Mycoses as compared to CYP2C19 *1/*1.

CYP2C19 CYP2C19*1, CYP2C19*2: CYP2C19 *2/*2 (assigned as poor metabolizer phenotype) is associated with increased dose-adjusted trough concentrations of voriconazole in children with Neoplasms as compared to CYP2C19 *1/*1 (assigned as normal metabolizer phenotype) .

CYP2C19 CYP2C19*1, CYP2C19*2: CYP2C19 *1/*2 (assigned as intermediate metabolizer phenotype) is associated with increased dose-adjusted trough concentrations of voriconazole in children with Neoplasms as compared to CYP2C19 *1/*1 (assigned as normal metabolizer phenotype) .

Side effects (1 finding)

Studies of side effects in people carrying a variant.

CYP2C19 CYP2C19*1, CYP2C19*2, CYP2C19*3, CYP2C19*17: CYP2C19 *1/*2 + *1/*3 + *2/*2 + *2/*3 + *3/*3 (assigned as intermediate metabolizer and poor metabolizer phenotype) is associated with increased concentrations of voriconazole in children with adverse events, Cholestasis or Thrombocytopenia as compared to CYP2C19 *1/*1 + *1/*17 (assigned as normal metabolizer phenotype) .

Study findings and evidence levels: PharmGKB (CC BY-SA 4.0). Guidelines: CPIC and DPWG, as bundled in PharmCAT. Most studies were done mainly in people of European ancestry.

Related Drugs

More drugs from the same category

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Agenerase (Protease Inhibitors)

Allegra (Antihistamines)

Not a prescribing recommendation. This page is educational information about pharmacogenomic research and clinical guidelines - it is not medical or dosing advice, and not a prediction of how any medication will work for you. Never start, stop, or change a medication or dose based on it; talk to your doctor or pharmacist, who can order clinical-grade testing if appropriate.

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Content updated September 2026.

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