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Fulvestrant

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

Fulvestrant is a selective estrogen receptor degrader (SERD) used to treat hormone receptor-positive breast cancer in postmenopausal women. It works by binding competitively to estrogen receptors, blocking the effects of estrogen that can promote cancer growth, and causing downregulation of the receptor. This medication is typically used when cancer has progressed after other anti-estrogen therapies.

Quick summary

Fulvestrant is an estrogen receptor antagonist used to treat hormone receptor-positive breast cancer by blocking estrogen from stimulating tumor growth.

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

Key facts at a glance

ATC
L02BA03
RxNorm
282357
Generic
Fulvestrant
Class
atc-l02
Brands
Faslodex, Cligavyx
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 (postmenopausal women with HR-positive breast cancer)intramuscular injection
Usual dose
500mg once monthly (after initial loading dose)
Maximum
consult physician
Frequency
once monthly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
adult (postmenopausal women - loading dose regimen)intramuscular injection
Usual dose
500mg on days 0, 14, 28, then monthly
Maximum
consult physician
Frequency
loading dose then monthly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (postmenopausal women with HR-positive breast cancer)intramuscular injection
Usual dose
500mg once monthly (no dose adjustment required)
Maximum
consult physician
Frequency
once monthly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Doses significantly higher than recommended therapeutic regimen (500mg loading dose) may cause serious toxicity
Chronic overdose: Repeated dosing exceeding recommended cumulative amount over treatment period leading to cumulative toxicity
Immediate actions
discontinue drug administration, monitor vital signs, supportive care, gastric decontamination if oral medications co-ingested
Antidote
no specific antidote(supportive care is primary treatment; no specific antidote available)
Poison Control: 1-800-222-1222

Special Populations

8 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

Fulvestrant should not be used during pregnancy unless clearly necessary. Women of childbearing potential should use effective contraception during treatment and for 2 years after the last dose.

Monitor

regular fetal monitoring

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

✗

pregnancy

second trimester
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

Discontinue fulvestrant if pregnancy occurs and advise patient on potential risks to fetus

Monitor

regular fetal monitoring and ultrasound assessments

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

Not recommended during third trimester; consider alternative therapies for breast cancer during pregnancy

Monitor

regular fetal monitoring

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

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

discontinue breastfeeding

Key Recommendations

It is unknown if fulvestrant is excreted in human breast milk. Breastfeeding should be discontinued during treatment and for 2 years after the last dose due to potential harm to the infant.

Monitor

no specific monitoring required

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

?

pediatric_age

children adolescents
unknown
FDA Category
N
Dose Adjustment

not established

Key Recommendations

Fulvestrant is not indicated for use in pediatric patients. Safety and efficacy have not been established in children or adolescents.

Monitor

not applicable

⚠

geriatric

elderly 65 plus
caution
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

No dose adjustment is required for patients over 65 years. However, elderly patients may have increased sensitivity to the drug and should be monitored closely for adverse effects.

Monitor

regular assessment of tolerability and adverse effects

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild moderate
caution
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

No dose adjustment is required for patients with mild to moderate renal impairment (CrCl 30-80 mL/min). Use with caution in patients with severe renal impairment.

Monitor

monitor renal function periodically

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild moderate
caution
FDA Category
N
Dose Adjustment

consider dose reduction

Key Recommendations

Fulvestrant is metabolized in the liver. For patients with mild to moderate hepatic impairment, no specific dose adjustment is required, but close monitoring is recommended. Use with caution.

Monitor

monitor liver function tests regularly

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2002

General prescribing information

drug_classWHO
2023

Drug class

Value:Selective Estrogen Receptor Degrader (SERD)

Drug class information

usageMedical guidelines
2023

Common uses

Value:Treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women

Common therapeutic uses

mechanismFDA
2023

Mechanism of action

Value:Selective estrogen receptor degrader (downregulates estrogen receptor)

Pharmacological mechanism

Treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. May be used alone or in combination with other targeted therapies.

Fulvestrant is a selective estrogen receptor degrader (SERD) that competitively binds to estrogen receptors with affinity comparable to estradiol. By binding to these receptors, it prevents estrogen from activating them, leading to receptor downregulation and inhibition of estrogen-dependent tumor growth.

Administered as intramuscular injections (typically 500mg on days 0, 14, and then monthly). Common side effects may include injection site pain, nausea, and hot flashes. Requires proper handling and administration by healthcare professionals. May increase risk of bleeding in patients taking anticoagulants.

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