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Abacavir / Lamivudine / Zidovudine

Published: July 27, 2026Updated: August 24, 2026

Abacavir/Lamivudine/Zidovudine is a triple-nucleoside reverse transcriptase inhibitor (NRTI) combination used to treat HIV-1 infection. This fixed-dose combination works by inhibiting the reverse transcriptase enzyme, preventing viral replication and reducing HIV viral load. It is typically prescribed as part of a comprehensive antiretroviral regimen for patients with HIV/AIDS.

Quick summary

A three-drug antiretroviral combination used to manage HIV infection by inhibiting viral replication.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 2026Editorial policy

Key facts at a glance

RxNorm
284620
Generic
Abacavir / Lamivudine / Zidovudine
Class
multi-ingredient
Brands
Trizivir
Availability
rx
Lactation
unknown
Routes
—
Forms
—
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
1 tablet (300mg/150mg/300mg) twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
1 tablet twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
1 tablet once daily or twice daily based on renal function
Maximum
consult physician
Frequency
once daily or every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose of 12 grams or more of the combined formulation may cause serious toxicity
Chronic overdose: Prolonged use above recommended doses may lead to cumulative toxicity including bone marrow suppression and lactic acidosis
Immediate actions
Gastric lavage within 1-2 hours of ingestion, activated charcoal administration, supportive care including intravenous fluids, monitoring of vital signs and organ function
Antidote
No specific antidote exists(Supportive care is the primary treatment; early intervention improves outcomes)
Poison Control: 1-800-222-1222

Special Populations

8 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

use only if benefits outweigh risks

Key Recommendations

consider alternative regimens; if used, continue throughout pregnancy to prevent vertical transmission

Monitor

regular fetal monitoring, viral load monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

continue therapy

Key Recommendations

antiretroviral therapy should be continued to reduce HIV transmission risk

Monitor

viral load monitoring, CD4 count, hematologic monitoring

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

avoid breastfeeding

Key Recommendations

HIV-positive mothers should not breastfeed regardless of therapy to prevent transmission

Monitor

not applicable

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

⚠

geriatric

elderly
caution
FDA Category
C
Dose Adjustment

no specific dose adjustment

Key Recommendations

use with caution due to increased susceptibility to adverse effects

Monitor

regular monitoring of renal function, hematologic parameters

Use with caution and monitor for adverse effects.

✗

pediatric_age

children under 12
contraindicated
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

fixed-dose combination not appropriate for pediatric dosing requirements

Monitor

not applicable

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

✗

renal_impairment

severe renal impairment
contraindicated
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

zidovudine and lamivudine require dose adjustment in renal impairment; fixed-dose combination cannot be dose-adjusted

Monitor

not applicable

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

✗

hepatic_impairment

moderate to severe
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

abacavir and zidovudine require dose adjustment in hepatic impairment

Monitor

liver function monitoring

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

✗

alcohol_users

chronic alcohol use
unsafe
FDA Category
C
Dose Adjustment

avoid concurrent use

Key Recommendations

alcohol increases risk of abacavir-associated lactic acidosis and hepatotoxicity

Monitor

liver function tests, lactate levels

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

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2001

Trizivir approval date by FDA

drug_classWHO
2023

Drug class

Value:Antiretroviral - Nucleoside Reverse Transcriptase Inhibitors (NRTIs)

Pharmacological classification of the fixed-dose combination

usageMedical guidelines
2023

Common uses

Value:HIV-1 infection treatment in adults and children

Primary therapeutic indication for the combination drug

dosageFDA
2023

Standard adult dose

Value:One tablet twice daily

Recommended dosing regimen for adult patients

Treatment of HIV-1 infection in adults and children weighing at least 40 kg, typically as part of combination antiretroviral therapy.

Each component is a nucleoside reverse transcriptase inhibitor (NRTI) that blocks HIV reverse transcriptase enzyme, preventing viral RNA from being converted to DNA, thereby inhibiting viral replication.

Carries boxed warnings for hypersensitivity reactions (particularly abacavir-related, especially in HLA-B*5701 positive patients) and lactic acidosis/hepatomegaly. Zidovudine component may cause bone marrow suppression and anemia. Requires HLA-B*5701 testing before initiating therapy. Not recommended for patients with hepatic impairment.

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 August 24, 2026. · Read our editorial policy