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Abacavir / Lamivudine

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

Abacavir/Lamivudine is a combination antiretroviral medication used to treat HIV-1 infection. It contains two nucleoside reverse transcriptase inhibitors that work together to suppress viral replication when used as part of a comprehensive antiretroviral regimen. This medication is typically prescribed for adults and children weighing at least 25 kg.

Quick summary

A two-drug antiretroviral combination tablet used once daily as part of HIV treatment regimens.

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

Key facts at a glance

RxNorm
614534
Generic
Abacavir / Lamivudine
Class
multi-ingredient
Brands
Epzicom
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
600mg/300mg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
weight-based dosing
Maximum
consult physician
Frequency
varies by weight
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
600mg/300mg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Doses exceeding 12 grams of the combined formulation may result in serious toxicity including lactic acidosis, hepatotoxicity, and cardiovascular collapse
Chronic overdose: Prolonged use above recommended doses can lead to cumulative mitochondrial toxicity, hepatic steatosis, and lactic acidosis
Immediate actions
Monitor vital signs, establish IV access, correct metabolic abnormalities, provide supportive care, consider gastric decontamination if within 1-2 hours of ingestion
Antidote
No specific antidote available(Treatment is supportive and symptomatic; 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

avoid use during first trimester unless benefits significantly outweigh potential fetal risks; consider alternative antiretroviral therapy

Monitor

regular prenatal monitoring, fetal ultrasound assessments

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

continue if already receiving, evaluate necessity

Key Recommendations

may continue therapy if already established; new initiations should weigh risks versus benefits

Monitor

routine prenatal care, viral load monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

continue therapy, do not discontinue

Key Recommendations

continue therapy to maintain viral suppression and reduce mother-to-child transmission risk

Monitor

HIV viral load monitoring, CD4 count, obstetric monitoring

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

HIV-infected mothers should not breastfeed to prevent HIV transmission regardless of antiretroviral therapy; both abacavir and lamivudine are excreted in breast milk

Monitor

infant HIV testing if breastfeeding occurs

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

no specific dose adjustment recommended, monitor closely

Key Recommendations

use with caution due to limited clinical experience in patients over 65 years; assess renal and hepatic function

Monitor

renal function, hepatic function, cardiovascular monitoring

Use with caution and monitor for adverse effects.

✗

pediatric_age

pediatric
unsafe
FDA Category
N
Dose Adjustment

not approved for pediatric use

Key Recommendations

fixed-dose combination not recommended for pediatric patients; use individual components with appropriate weight-based dosing

Monitor

weight-based dosing, monitoring for adverse effects

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

⚠

renal_impairment

renal impairment mild
caution
FDA Category
N
Dose Adjustment

dose adjustment required for lamivudine component

Key Recommendations

not recommended in patients with creatinine clearance below 50 mL/min; use individual components with adjusted dosing

Monitor

renal function monitoring (creatinine clearance)

Use with caution and monitor for adverse effects.

✗

renal_impairment

renal impairment severe
unsafe
FDA Category
N
Dose Adjustment

contraindicated

Key Recommendations

avoid fixed-dose combination in severe renal impairment; use individual components with significant dose reduction

Monitor

frequent renal function monitoring

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

Statistics and clinical data

prescribingFDA
2023

Commonly prescribed since

Value:2004

FDA approval year for Abacavir/Lamivudine combination (Epzicom)

drug_classWHO
2023

Drug class

Value:Antiretroviral / NRTI

Nucleoside Reverse Transcriptase Inhibitor combination drug

usageMedical guidelines
2023

Common uses

Value:HIV-1 infection treatment

Used in combination with other antiretrovirals for HIV management

mechanismFDA
2023

Mechanism of action

Value:Inhibits reverse transcriptase

Both abacavir and lamivudine are nucleoside analog reverse transcriptase inhibitors

Treatment of HIV-1 infection in combination with other antiretroviral agents. Not indicated for HIV-2 infection.

Both abacavir and lamivudine are nucleoside reverse transcriptase inhibitors that compete with natural nucleotides, blocking the activity of HIV reverse transcriptase and preventing the conversion of viral RNA to DNA, thereby inhibiting viral replication.

Requires HLA-B*5701 testing before initiation due to risk of severe hypersensitivity reaction. Should be discontinued immediately if hypersensitivity is suspected. Not recommended for patients with hepatic impairment. May cause lactic acidosis and hepatomegaly with steatosis. Once-daily dosing improves adherence.

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