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Amprenavir

Published: July 26, 2026Updated: August 20, 2026

Amprenavir is an antiretroviral medication belonging to the protease inhibitor class, used in combination with other antiretrovirals for the treatment of HIV-1 infection. It works by inhibiting the HIV protease enzyme, which is essential for viral replication. While once used in HIV management, amprenavir has since been largely replaced by newer formulations such as fosamprenavir.

Quick summary

Amprenavir is an HIV protease inhibitor (now largely discontinued) that was used in combination therapy to treat HIV-1 infection.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ATC
J05AE05
RxNorm
228656
Generic
Amprenavir
Class
atc-j05
Brands
—
Availability
rx
Lactation
unknown
Routes
oral
Forms
solution, capsule
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
1200mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
20mg/kg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
1200mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Dose at which significant toxicity is expected based on therapeutic dosing (1200mg daily)
Chronic overdose: Cumulative dosing exceeding recommended 1200mg daily regimen over extended period
Immediate actions
Supportive care, gastric decontamination if within 1-2 hours, monitor hepatic and renal function
Antidote
No specific antidote available(Supportive care is mainstay of treatment; no proven antidote)
Poison Control: 1-800-222-1222

Special Populations

9 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

use only if clearly needed

Key Recommendations

avoid in pregnancy unless potential benefits outweigh potential risks to fetus

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use only if clearly needed

Key Recommendations

continue only if benefits justify risks

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

use only if clearly needed

Key Recommendations

continue only if benefits justify risks

Monitor

regular prenatal monitoring and viral load monitoring

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

HIV-infected mothers should not breastfeed to avoid HIV transmission to infant regardless of antiretroviral therapy

Monitor

none while breastfeeding on this medication

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

no specific adjustment, use with caution

Key Recommendations

limited clinical experience in patients over 65 years, use with close monitoring

Monitor

monitor for adverse effects and organ function

Use with caution and monitor for adverse effects.

✓

pediatric_age

children 2 12 years
safe
FDA Category
N
Dose Adjustment

weight-based dosing required

Key Recommendations

approved for pediatric patients age 2 years and older; oral solution not for use in infants under 2 years

Monitor

monitor growth, development, and adverse effects

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

amprenavir is not significantly renally excreted, no dose adjustment needed for mild to moderate renal impairment

Monitor

standard monitoring

⚠

hepatic_impairment

mild
caution
FDA Category
N
Dose Adjustment

consider dose reduction

Key Recommendations

use with caution in mild hepatic impairment, monitor liver function

Monitor

regular liver function tests

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

dose reduction recommended

Key Recommendations

reduce dose in moderate to severe hepatic impairment; use with close monitoring

Monitor

frequent liver function tests and drug level monitoring if available

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1999

FDA approval timeline for Amprenavir

drug_classWHO
2023

Drug class

Value:HIV protease inhibitor (antiretroviral)

Drug class classification for Amprenavir

usageMedical guidelines
2023

Primary indication

Value:HIV-1 infection treatment

Primary therapeutic use of Amprenavir

pharmacokineticsFDA
2023

Bioavailability

Value:~90%

Absorption and bioavailability information

Treatment of HIV-1 infection in combination with other antiretroviral agents. It was indicated for both treatment-naive and treatment-experienced patients when used as part of a comprehensive antiretroviral regimen.

Amprenavir is an HIV-1 protease inhibitor that works by blocking the HIV protease enzyme, which is necessary for the virus to mature and become infectious. By preventing proper viral protein processing, it inhibits the replication of HIV.

Amprenavir has been discontinued and is no longer marketed, having been largely replaced by fosamprenavir (a prodrug with improved tolerability). Common side effects included rash, nausea, and diarrhea. It had significant pill burden requiring multiple daily doses. Patients should use current FDA-approved HIV medications as recommended by their healthcare provider.

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 20, 2026. · Read our editorial policy