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Tocilizumab

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

Tocilizumab is a monoclonal antibody that targets and blocks interleukin-6 (IL-6) receptors, reducing inflammation in conditions where IL-6 plays a key role. It is used to treat autoimmune and inflammatory disorders such as rheumatoid arthritis, giant cell arteritis, and severe COVID-19.

Quick summary

Tocilizumab is an IL-6 receptor antagonist used to treat inflammatory conditions by blocking the pro-inflammatory cytokine IL-6.

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
L04AC07
RxNorm
612865
Generic
Tocilizumab
Class
atc-l04
Brands
Tyenne, Tofidence, Avtozma, Actemra
Availability
rx
Lactation
unknown
Routes
—
Forms
prefilled syringe, 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)tablet
Usual dose
162mg once weekly
Maximum
consult physician
Frequency
once weekly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
162mg once weekly
Maximum
consult physician
Frequency
once weekly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
162mg once weekly
Maximum
consult physician
Frequency
once weekly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose significantly exceeding recommended 8mg/kg IV infusion may cause serious toxicity
Chronic overdose: Cumulative dosing exceeding recommended regimen over extended periods may lead to increased immunosuppression and infections
Immediate actions
Discontinue infusion, monitor vital signs, supportive care, monitor for infections
Antidote
No specific antidote available(Treatment is supportive; no specific antidote exists)
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

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

⚠

pregnancy

second and third trimester
caution
FDA Category
C
Dose Adjustment

use only if benefits outweigh risks

Key Recommendations

continue only if already receiving therapy for maternal condition requiring ongoing treatment

Monitor

regular fetal monitoring and growth assessments

Use with caution and monitor for adverse effects.

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

decision to discontinue drug or breastfeeding should consider benefit to infant and mother

Monitor

monitor infant for infections

⚠

geriatric

elderly over 65
caution
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

use standard dosing but monitor for increased risk of infections

Monitor

regular monitoring for infections and gastrointestinal perforation

Use with caution and monitor for adverse effects.

✓

pediatric_age

children 2 years and older
safe
FDA Category
N
Dose Adjustment

weight-based dosing required

Key Recommendations

approved for polyarticular juvenile idiopathic arthritis and systemic juvenile idiopathic arthritis

Monitor

monitor growth, development and infection symptoms

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no dose adjustment needed

Key Recommendations

can be used at standard dosing in mild to moderate renal impairment

Monitor

routine renal function monitoring

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

limited data available, use only if benefits outweigh risks

Monitor

more frequent renal function monitoring

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

monitor liver enzymes closely, may require dose interruption

Monitor

regular liver function test monitoring

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

severe
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

contraindicated in severe hepatic impairment

Monitor

liver function monitoring if accidentally used

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

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2010

Initial FDA approval for Actemra

drug_classWHO
2023

Drug class

Value:IL-6 receptor antagonist

Monoclonal antibody IL-6 inhibitor

usageFDA
2023

Common uses

Value:Rheumatoid arthritis, COVID-19, giant cell arteritis, systemic sclerosis

Approved therapeutic indications

mechanismFDA
2023

Mechanism of action

Value:IL-6 receptor blockade

Pharmacodynamic mechanism

Tocilizumab is used to treat moderate to severe rheumatoid arthritis (in adults and children), systemic juvenile idiopathic arthritis, polyarticular juvenile idiopathic arthritis, giant cell arteritis, systemic sclerosis-associated interstitial lung disease, and severe COVID-19. It may also be used for cytokine release syndrome associated with CAR-T cell therapy.

Tocilizumab binds to both soluble and membrane-bound IL-6 receptors (sIL-6R and mIL-6R), preventing IL-6 from attaching to these receptors. This inhibits IL-6-mediated inflammatory signaling, reducing the immune response that causes tissue damage and symptoms in inflammatory conditions.

Tocilizumab increases infection risk, including tuberculosis and serious bacterial, fungal, and viral infections. Live vaccines should be avoided during treatment. Regular monitoring of blood counts and liver function may be required. It is administered as an intravenous infusion, typically every 4 weeks.

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