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Ixekizumab (Taltz): A Patient’s Guide

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

Ixekizumab is a prescription biologic medicine that blocks an immune protein called IL-17A. It is used to treat plaque psoriasis and certain forms of psoriatic arthritis or spondyloarthritis, including ankylosing spondylitis and non-radiographic axial spondyloarthritis.

Quick summary

Ixekizumab can help reduce symptoms of inflammatory skin and joint conditions, usually with regular injections. Your doctor or pharmacist should confirm whether it is appropriate for you and teach you how to use it safely.

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

Key facts at a glance

ATC
L04AC13
RxNorm
1745099
Generic
Ixekizumab
Class
atc-l04
Brands
Taltz
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
160 mg initial dose, then 80 mg
Maximum
consult physician
Frequency
every 2 weeks for 12 weeks, then every 4 weeks
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)subcutaneous injection
Usual dose
160 mg initial dose, then 80 mg
Maximum
consult physician
Frequency
every 2 weeks for 12 weeks, then every 4 weeks
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)subcutaneous injection
Usual dose
160 mg initial dose, then 80 mg
Maximum
consult physician
Frequency
every 2 weeks for 12 weeks, then every 4 weeks
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose exceeding 320 mg may cause significant adverse effects; standard doses are 80-160 mg
Chronic overdose: Long-term excessive dosing may increase risk of infections and immune suppression
Immediate actions
Monitor vital signs, provide supportive care, observe for infections
Antidote
No specific antidote available(Supportive care is primary treatment; no specific reversal agent exists)
Poison Control: 1-800-222-1222

Special Populations

11 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

Ixekizumab should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus

Monitor

regular prenatal care and fetal monitoring

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 clearly needed, consider risks vs benefits

Monitor

standard prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

Consider discontinuing therapy near end of pregnancy due to potential immune suppression in newborn

Monitor

monitor newborn for infections

Use with caution and monitor for adverse effects.

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

It is unknown whether ixekizumab is present in human milk or if it is absorbed systemically by the infant. A decision should be made whether to discontinue breastfeeding or to discontinue the drug

Monitor

monitor infant for infections

✓

pediatric_age

adolescents
safe
FDA Category
N
Dose Adjustment

no adjustment for age 12 and older

Key Recommendations

Approved for pediatric plaque psoriasis in patients 6 years and older. Dosing differs by weight for younger children

Monitor

regular assessment of growth and development

✓

pediatric_age

children
safe
FDA Category
N
Dose Adjustment

weight-based dosing for children under 50kg

Key Recommendations

For pediatric patients 6 to less than 18 years with moderate to severe plaque psoriasis, dosing is weight-based

Monitor

monitor for infections and tuberculosis

✓

geriatric

elderly
safe
FDA Category
N
Dose Adjustment

no specific dose adjustment required

Key Recommendations

No overall differences in efficacy or safety observed in clinical trials for patients 65 years and older

Monitor

standard geriatric monitoring including infection surveillance

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

Ixekizumab is a monoclonal antibody and is not eliminated by renal pathways

Monitor

standard renal function monitoring

✓

renal_impairment

severe
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

Limited data available for severe renal impairment but not expected to require dose adjustment

Monitor

standard monitoring

✓

hepatic_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

Ixekizumab is metabolized via proteolysis and not through hepatic pathways

Monitor

standard hepatic function monitoring

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

Limited clinical data in severe hepatic impairment; use only if benefits outweigh risks

Monitor

close monitoring of liver function

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classFDA
2023

Drug class

Value:IL-17A inhibitor (Biologic)

Ixekizumab is a monoclonal antibody that inhibits interleukin-17A

usageFDA
2023

Common uses

Value:Plaque psoriasis, psoriatic arthritis, ankylosing spondylitis

FDA-approved therapeutic indications

regulatoryFDA
2023

FDA approval year

Value:2016

Initial FDA approval date for Ixekizumab (Taltz)

administrationFDA
2023

Route of administration

Value:Subcutaneous injection

Method of drug delivery

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