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Fondaparinux

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

Fondaparinux is a synthetic anticoagulant that works by selectively inhibiting Factor Xa through its binding to antithrombin III, preventing blood clot formation. It is primarily used for the prevention and treatment of venous thromboembolic events, including deep vein thrombosis and pulmonary embolism, particularly in patients undergoing major orthopedic surgery or those at risk of blood clots.

Quick summary

Fondaparinux is a injectable anticoagulant that prevents blood clots by inhibiting Factor Xa, used primarily for preventing and treating venous thromboembolism.

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

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
B01AX05
RxNorm
321208
Generic
Fondaparinux
Class
atc-b01
Brands
Arixtra
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
2.5mg once daily (prophylaxis) or 5mg once daily (VTE treatment)
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)subcutaneous injection
Usual dose
Not typically recommended; limited pediatric data available
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)subcutaneous injection
Usual dose
2.5mg once daily (prophylaxis) with caution due to renal function
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 that may cause serious bleeding toxicity
Chronic overdose: prolonged use with accumulation leading to increased bleeding risk
Immediate actions
discontinue drug, monitor vital signs, supportive care, consider platelet transfusion
Antidote
no specific antidote available(supportive care and bleeding management only)
Poison Control: 1-800-222-1222

Special Populations

9 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring and ultrasound assessments

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

✗

pregnancy

second trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use unless benefits outweigh risks, consider alternative anticoagulants

Monitor

regular fetal monitoring, ultrasound for fetal growth

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

discontinue before delivery if possible, avoid close to delivery

Monitor

fetal monitoring, careful delivery planning, assess bleeding risk

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

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

discontinue breastfeeding or avoid drug

Key Recommendations

fondaparinux is excreted in breast milk, breastfeeding should be discontinued during treatment

Monitor

no specific monitoring required if breastfeeding discontinued

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce starting dose, use lower therapeutic doses

Key Recommendations

use with caution due to increased bleeding risk, start at lower end of dosing range

Monitor

regular renal function monitoring, watch for signs of bleeding, frequent CBC checks

Use with caution and monitor for adverse effects.

?

pediatric_age

children adolescents
unknown
FDA Category
N
Dose Adjustment

not established for pediatric use

Key Recommendations

not recommended for use in children under 18 years due to limited safety and efficacy data

Monitor

no standard monitoring established, use only in specialized pediatric centers

✗

renal_impairment

severe
contraindicated
FDA Category
N
Dose Adjustment

do not use in severe impairment

Key Recommendations

contraindicated in patients with severe renal impairment (CrCl less than 30 mL/min)

Monitor

assess renal function before initiating therapy

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

⚠

renal_impairment

moderate
caution
FDA Category
N
Dose Adjustment

use with caution, consider dose reduction

Key Recommendations

use with caution in moderate renal impairment (CrCl 30-50 mL/min), monitor closely

Monitor

frequent renal function monitoring, monitor for signs of bleeding

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with extreme caution, may require dose reduction

Key Recommendations

use with caution in severe hepatic impairment due to coagulopathy risk

Monitor

monitor liver function, coagulation parameters, watch for bleeding

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2001

FDA approval year for Fondaparinux (Arixtra)

drug_classWHO
2023

Drug class

Value:Anticoagulant - Synthetic pentasaccharide - Selective Factor Xa inhibitor

Pharmacological classification of Fondaparinux

usageMedical guidelines
2023

Common uses

Value:Prevention and treatment of venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE)

Primary therapeutic indications

mechanismFDA
2023

Mechanism of action

Value:Selectively inhibits Factor Xa by binding to antithrombin III

Pharmacodynamic mechanism

Prevention of venous thromboembolic events (VTE) in patients undergoing major orthopedic surgery of the legs or hips; treatment of acute DVT and pulmonary embolism; sometimes used in acute coronary syndromes.

Fondaparinux selectively binds to antithrombin III, potentiating its ability to neutralize Factor Xa by approximately 300-fold, thereby interrupting the coagulation cascade and preventing thrombin generation and clot formation.

Administered as a once-daily subcutaneous injection. Contraindicated in patients with severe renal impairment, active bleeding, or bacterial endocarditis. Requires careful monitoring for bleeding complications and may increase risk of spinal/epidural hematoma in patients undergoing neuraxial anesthesia.

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