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Abacavir

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

Abacavir is an antiretroviral medication used in combination with other drugs to treat HIV infection. It belongs to a class of drugs called nucleoside reverse transcriptase inhibitors (NRTIs) and is available in multiple formulations for use in adults and children.

Quick summary

Abacavir is an HIV medication that works by inhibiting the reverse transcriptase enzyme, preventing the virus from replicating.

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
J05AF06
RxNorm
190521
Generic
Abacavir
Class
atc-j05
Brands
Triumeq, Ziagen, Trizivir, Epzicom
Availability
rx
Lactation
unknown
Routes
oral
Forms
tablet, solution
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
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
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 approximately 20 times the recommended daily dose that may cause serious toxicity
Chronic overdose: Prolonged use above recommended doses may lead to cumulative toxicity including lactic acidosis and hepatomegaly with steatosis
Immediate actions
Administer activated charcoal if presentation within 1 hour, gastric lavage may be considered if large dose ingested within 1-2 hours, provide supportive care and monitor vital functions
Antidote
No specific antidote available(Supportive care is the primary treatment; early intervention improves outcomes)
Poison Control: 1-800-222-1222

Special Populations

10 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

use only if clearly needed and benefits outweigh potential risks

Monitor

regular prenatal care and fetal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

continue therapy if HIV treatment required

Monitor

routine prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

maintain HIV suppression through delivery

Monitor

regular monitoring until delivery

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

HIV-positive mothers should not breastfeed to avoid vertical transmission

Monitor

not applicable

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

✓

pediatric_age

infants 3 months and older
safe
FDA Category
C
Dose Adjustment

weight-based dosing

Key Recommendations

use pediatric formulation; requires HLA-B*5701 testing before initiation

Monitor

monitor for hypersensitivity reactions

⚠

geriatric

over 65 years
caution
FDA Category
C
Dose Adjustment

start at lower end of dosing range

Key Recommendations

use with caution; monitor renal and hepatic function

Monitor

regular monitoring of liver function and renal function

Use with caution and monitor for adverse effects.

✓

renal_impairment

mild to moderate
safe
FDA Category
C
Dose Adjustment

no dose adjustment required

Key Recommendations

no specific dose adjustment needed for mild-moderate renal impairment

Monitor

standard monitoring

⚠

renal_impairment

severe
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

limited data for severe renal impairment; consider monitoring

Monitor

monitor drug levels if available

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild
caution
FDA Category
C
Dose Adjustment

dose reduction may be required

Key Recommendations

use reduced dose; monitor closely

Monitor

frequent liver function monitoring

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

moderate to severe
contraindicated
FDA Category
C
Dose Adjustment

contraindicated

Key Recommendations

do not use in moderate-severe hepatic impairment

Monitor

not applicable

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

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1998

FDA approval for HIV treatment

drug_classWHO
2023

Drug class

Value:Nucleoside Reverse Transcriptase Inhibitor (NRTI)

Antiretroviral drug class

usageMedical guidelines
2023

Common uses

Value:HIV-1 infection treatment

Primary therapeutic indication

formulationFDA
2023

Available formulations

Value:Oral tablets, oral solution

Available dosage forms

Treatment of HIV-1 infection in combination with other antiretroviral agents. It is indicated for use in adult and pediatric patients.

Abacavir is a synthetic carbocyclic nucleoside analog that inhibits the activity of HIV-1 reverse transcriptase by competing with the natural substrate and incorporating into the growing viral DNA chain, which results in chain termination.

All patients should be screened for HLA-B*5701 before starting therapy due to risk of severe hypersensitivity reactions. Should not be used as monotherapy. Common side effects include nausea, headache, and fatigue. Liver function monitoring may be required.

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