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Faricimab

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

Faricimab is a humanized bispecific antibody injection medication used to treat certain retinal eye conditions. It works by simultaneously inhibiting two pathways (VEGF-A and Ang-2) that contribute to abnormal blood vessel growth and fluid leakage in the retina. This medication is used in adults with neovascular (wet) age-related macular degeneration, diabetic macular edema, and macular edema following retinal vein occlusion.

Quick summary

Faricimab is an eye injection that treats retinal conditions by blocking two pathways involved in abnormal blood vessel growth and fluid leakage.

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

Key facts at a glance

ATC
S01LA09
RxNorm
2591519
Generic
Faricimab
Class
atc-s01
Brands
Vabysmo
Availability
rx
Lactation
unknown
Routes
—
Forms
injection, prefilled syringe
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)intravitreal injection
Usual dose
6mg (0.05mL of 120mg/mL solution)
Maximum
consult physician
Frequency
every 4 weeks for first 4 doses, then every 8-16 weeks based on response
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (not applicable)intravitreal injection
Usual dose
not approved for pediatric use
Maximum
consult physician
Frequency
not applicable
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)intravitreal injection
Usual dose
6mg (0.05mL of 120mg/mL solution)
Maximum
consult physician
Frequency
every 4 weeks for first 4 doses, then every 8-16 weeks based on response
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Doses significantly above the recommended 6 mg intravitreal dose may cause serious ocular toxicity
Chronic overdose: Not well established due to limited systemic absorption and professional administration
Immediate actions
Immediate ophthalmologic evaluation, monitor intraocular pressure, intraocular antibiotics if infection suspected
Antidote
No specific antidote exists for faricimab(N/A - treatment is supportive and symptom-directed)
Poison Control: 1-800-222-1222

Special Populations

8 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks to the mother

Monitor

regular fetal monitoring recommended

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if clearly needed, discuss risks and benefits with patient

Monitor

regular prenatal check-ups

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

consider delaying treatment until after delivery if clinically appropriate

Monitor

regular fetal monitoring

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

discontinue breastfeeding or interrupt treatment, decision should be based on importance of drug to mother

Monitor

monitor infant for potential effects

Use with caution and monitor for adverse effects.

✓

geriatric

elderly
safe
FDA Category
N
Dose Adjustment

no dosage adjustment required

Key Recommendations

safe for use in elderly patients, commonly used for age-related macular degeneration

Monitor

routine ophthalmologic monitoring

?

pediatric_age

children 0 18
unknown
FDA Category
N
Dose Adjustment

not established

Key Recommendations

use only if benefits outweigh potential risks, limited clinical trial data in pediatric populations

Monitor

close ophthalmologic monitoring

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no dosage adjustment needed

Key Recommendations

no specific adjustments required due to intravitreal administration and minimal systemic absorption

Monitor

standard monitoring

✓

hepatic_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no dosage adjustment needed

Key Recommendations

no specific adjustments required due to minimal systemic exposure

Monitor

standard monitoring

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2022

Initial FDA approval date for Faricimab (Vabysmo)

drug_classFDA
2023

Drug class

Value:VEGF and Ang-2 bispecific inhibitor

Pharmacological classification of Faricimab

usageFDA
2023

Primary indications

Value:Wet age-related macular degeneration, diabetic macular edema

Therapeutic indications for Faricimab

administrationFDA
2023

Route of administration

Value:Intravitreal injection

Method of drug administration

Faricimab is indicated for the treatment of neovascular (wet) age-related macular degeneration (AMD), diabetic macular edema (DME), and macular edema following retinal vein occlusion (RVO). It is administered as an intravitreal injection by an eye care professional.

Faricimab is a bispecific antibody that binds to and inhibits both VEGF-A and Ang-2. By blocking VEGF-A, it reduces endothelial cell proliferation, abnormal blood vessel growth (neovascularization), and vascular leakage. By inhibiting Ang-2, it promotes vascular stability and reduces inflammation, providing a dual mechanism for treating retinal vascular diseases.

Faricimab is administered by injection into the eye (intravitreal injection) by a qualified healthcare professional in a clinical setting. Common side effects may include conjunctival hemorrhage, eye discomfort, and increased intraocular pressure. Patients should report any signs of infection (pain, redness, sensitivity to light, vision changes) immediately. Treatment intervals may be adjusted based on individual response, with some patients potentially extending intervals up to every 16 weeks after initial dosing.

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