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Anti-Inhibitor Coagulant Complex

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

Anti-Inhibitor Coagulant Complex (FEIBA) is a bypassing agent used to treat and prevent bleeding in hemophilia A or B patients who have developed inhibitors (neutralizing antibodies) against factor VIII or IX replacement therapy. It contains a combination of activated and non-activated clotting factors that work around these inhibitors to promote blood coagulation.

Quick summary

A hemostatic agent for hemophilia patients with inhibitor antibodies that bypasses the need for specific clotting factors.

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
B02BD01
RxNorm
314504
Generic
Anti-Inhibitor Coagulant Complex
Class
atc-b02
Brands
Feiba
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
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)intravenous infusion
Usual dose
50-100 units/kg
Maximum
consult physician
Frequency
every 12-48 hours as needed
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)intravenous infusion
Usual dose
50-100 units/kg
Maximum
consult physician
Frequency
every 12-48 hours as needed
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)intravenous infusion
Usual dose
50-75 units/kg
Maximum
consult physician
Frequency
every 12-48 hours as needed
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity including thromboembolic events
Chronic overdose: cumulative dosing exceeding recommended limits can lead to thrombotic complications
Immediate actions
discontinue infusion, monitor vital signs, provide supportive care
Antidote
no specific antidote available(supportive care is primary treatment)
Poison Control: 1-800-222-1222

Special Populations

8 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

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

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use only if clearly needed

Key Recommendations

use only if benefits outweigh risks to mother

Monitor

regular fetal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

use only if clearly needed

Key Recommendations

use only if benefits outweigh risks to mother; plan for delivery

Monitor

regular fetal monitoring and delivery planning

Use with caution and monitor for adverse effects.

?

lactation

breastfeeding
unknown
FDA Category
C
Dose Adjustment

avoid or discontinue breastfeeding

Key Recommendations

discontinue breastfeeding or avoid use due to unknown excretion in breast milk

Monitor

monitor infant for bleeding

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

adjust based on renal and hepatic function

Key Recommendations

use with caution; assess renal and hepatic function before dosing

Monitor

monitor renal function, hepatic function, and for signs of thrombosis

Use with caution and monitor for adverse effects.

⚠

pediatric_age

children
caution
FDA Category
C
Dose Adjustment

weight-based dosing required

Key Recommendations

dosing based on body weight; use under close medical supervision

Monitor

monitor for bleeding, thrombosis, and inhibitor development

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe renal impairment
caution
FDA Category
C
Dose Adjustment

reduce dose or avoid use

Key Recommendations

use with caution; consider dose reduction based on CrCl

Monitor

monitor renal function and for signs of accumulation

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate hepatic impairment
caution
FDA Category
C
Dose Adjustment

reduce dose or avoid use

Key Recommendations

use with caution; may require dose reduction

Monitor

monitor hepatic function and coagulation parameters

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1980

FDA approval date for Feiba (Anti-Inhibitor Coagulant Complex)

drug_classWHO
2023

Drug class

Value:Bypassing agent

Pharmacological classification of Anti-Inhibitor Coagulant Complex

usageMedical guidelines
2023

Primary indication

Value:Treatment of bleeding episodes in hemophilia patients with inhibitors

Main therapeutic use for patients with factor VIII or IX inhibitors

mechanismMedical literature
2023

Mechanism of action

Value:Bypasses factor VIII inhibitors to promote clotting

How the drug works to achieve hemostasis

Treatment and prevention of bleeding in patients with hemophilia A or B who have developed inhibitors to factor VIII or IX. May also be used for acquired hemophilia and other bleeding disorders with inhibitor presence.

Contains multiple coagulation factors (mainly non-activated factors II, IX, X and activated factor VII) that interact with plasma clotting factors and platelets to generate thrombin, bypassing the need for factors VIII or IX that are inhibited.

Regular monitoring for thrombotic events is required. Not interchangeable with other hemophilia products. Treatment should be supervised by a hematologist. May cause allergic reactions including anaphylaxis. Efficacy may vary between patients.

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