Skip to content

Fremanezumab

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

Fremanezumab is a monoclonal antibody medication used for the preventive treatment of migraine in adults. It works by targeting and blocking calcitonin gene-related peptide (CGRP), a protein involved in migraine attacks. This treatment is administered by subcutaneous injection and is typically prescribed for patients who experience chronic or episodic migraine.

Quick summary

Fremanezumab is a CGRP inhibitor injection used to prevent migraine headaches in adults.

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

Key facts at a glance

ATC
N02CD03
RxNorm
2056691
Generic
Fremanezumab
Class
atc-n02
Brands
Ajovy
Availability
rx
Lactation
unknown
Routes
—
Forms
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)subcutaneous injection
Usual dose
225mg monthly
Maximum
consult physician
Frequency
once monthly (or 675mg every 3 months)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)subcutaneous injection
Usual dose
Not FDA approved for pediatric use
Maximum
consult physician
Frequency
N/A
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)subcutaneous injection
Usual dose
225mg monthly
Maximum
consult physician
Frequency
once monthly (or 675mg every 3 months)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Dose significantly above recommended therapeutic regimen (225mg monthly or 675mg quarterly)
Chronic overdose: Prolonged elevation of CGRP blockade with potential for enhanced pharmacological effects
Immediate actions
Discontinue administration, monitor vital signs, provide supportive care, contact poison control
Antidote
No specific antidote available(Supportive care is primary treatment approach)
Poison Control: 1-800-222-1222

Special Populations

10 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh potential risks to fetus

Monitor

regular prenatal monitoring recommended

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

continue only if benefits outweigh potential risks

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh potential risks

Monitor

regular fetal monitoring

Use with caution and monitor for adverse effects.

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

discontinue breastfeeding or interrupt treatment based on benefit-risk assessment

Monitor

monitor infant for potential effects

✗

pediatric_age

under 18 years
unsafe
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

not approved for use in pediatric patients; safety and efficacy not established

Monitor

not applicable

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

✓

geriatric

65 years and older
safe
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

no dosage adjustment required; monitor for adverse effects

Monitor

routine monitoring

✓

renal_impairment

mild moderate
safe
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

no dose adjustment required for mild to moderate renal impairment

Monitor

routine monitoring

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

use with caution; limited clinical data available

Monitor

enhanced monitoring recommended

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild moderate
safe
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

no dose adjustment required for mild to moderate hepatic impairment

Monitor

routine monitoring

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

use with caution; limited clinical data available

Monitor

enhanced monitoring recommended

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classFDA
2018

Drug class

Value:CGRP inhibitor

Calcitonin gene-related peptide inhibitor monoclonal antibody

prescribingFDA
2018

FDA approval year

Value:2018

Initial FDA approval for Fremanezumab

usageFDA
2023

Common uses

Value:Migraine prevention

Approved therapeutic indication for episodic and chronic migraine

administrationFDA
2023

Route of administration

Value:Subcutaneous injection

Method of drug delivery

Fremanezumab is indicated for the preventive treatment of migraine in adults, including both chronic migraine (15 or more headache days per month) and episodic migraine (fewer than 15 headache days per month).

Fremanezumab is a humanized monoclonal antibody that binds specifically to the calcitonin gene-related peptide (CGRP) ligand, preventing CGRP from binding to its receptor. By blocking this neuropeptide, which is involved in the inflammation and pain signaling associated with migraines, the medication helps reduce the frequency and severity of migraine attacks.

Fremanezumab is administered as a subcutaneous injection, either monthly or quarterly. As a biologic medication, it should not be stopped abruptly without medical consultation. Common side effects may include injection site reactions. Patients should be monitored for hypersensitivity reactions during treatment.

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