Skip to content

Didanosine

Published: July 26, 2026Updated: August 24, 2026

Didanosine is an antiretroviral medication classified as a nucleoside reverse transcriptase inhibitor (NRTI) used in combination with other drugs to treat HIV-1 infection. It works by inhibiting the reverse transcriptase enzyme that HIV needs to replicate, helping to reduce viral load and slow disease progression. This medication has largely been replaced by newer, better-tolerated options in modern HIV treatment regimens.

Quick summary

Didanosine is an older HIV medication that inhibits viral replication by blocking the reverse transcriptase enzyme.

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

Key facts at a glance

ATC
J05AF02
RxNorm
3364
Generic
Didanosine
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
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 exceeding 10 grams may cause serious toxicity, significantly above the therapeutic daily dose of 400mg
Chronic overdose: Cumulative daily doses exceeding recommended amounts can lead to lactic acidosis, hepatomegaly with steatosis, pancreatitis, and peripheral neuropathy
Immediate actions
Gastric lavage within 1-2 hours of ingestion, activated charcoal administration, supportive care, monitor vital signs and organ function
Antidote
No specific antidote available(Supportive care is primary treatment; no antidote proven highly effective)
Poison Control: 1-800-222-1222

Special Populations

6 groups
⚠

pregnancy

general pregnancy
caution
FDA Category
B
Dose Adjustment

continue if needed for maternal health

Key Recommendations

use only if clearly needed for maternal HIV treatment; consider switching to alternatives with more pregnancy safety data

Monitor

regular prenatal monitoring and viral load tracking

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 regardless of ART status to prevent transmission

Monitor

N/A

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

⚠

pediatric_age

children 6 months and older
caution
FDA Category
N
Dose Adjustment

weight-based dosing required

Key Recommendations

dose based on body surface area; monitor for pancreatic toxicity and peripheral neuropathy

Monitor

regular monitoring of amylase, lipase, and neurological symptoms

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly 65 years and older
caution
FDA Category
N
Dose Adjustment

start at lower end of dosing range

Key Recommendations

use with caution due to age-related decline in renal and hepatic function; monitor for adverse effects

Monitor

regular renal function, liver function, and pancreatic enzyme monitoring

Use with caution and monitor for adverse effects.

✗

renal_impairment

severe creatinine clearance below 30 ml min
unsafe
FDA Category
N
Dose Adjustment

significant dose reduction required; contraindicated in some formulations

Key Recommendations

dose adjustment essential; consider alternative agents; avoid using extended-release formulation in severe impairment

Monitor

frequent renal function monitoring and drug level monitoring if available

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

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

may require dose reduction

Key Recommendations

use with caution; monitor liver function tests closely

Monitor

regular hepatic function monitoring

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1991

Original FDA approval date for Didanosine (Videx)

drug_classWHO
2023

Drug class

Value:Nucleoside Reverse Transcriptase Inhibitor (NRTI)

Antiretroviral drug class classification

usageFDA
2023

Primary indication

Value:HIV-1 infection treatment

Primary therapeutic use for Didanosine

safetyFDA
2023

Black Box Warning

Value:Pancreatitis, lactic acidosis

Serious adverse reactions requiring warning

Didanosine is indicated for the treatment of HIV-1 infection in combination with other antiretroviral agents. It is typically used when other NRTIs cannot be tolerated or are contraindicated.

Didanosine is a nucleoside analog that gets incorporated into the growing viral DNA chain during HIV replication. Once incorporated, it causes chain termination because it lacks the necessary structure for continued DNA synthesis, thereby inhibiting viral replication.

Didanosine must be taken on an empty stomach for optimal absorption. Common serious side effects include pancreatitis and peripheral neuropathy. It may also cause lactic acidosis and hepatomegaly. Regular monitoring of pancreatic enzymes and nerve function is recommended during treatment.

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

WellAlly may earn a referral fee from linked resources at no extra cost to you. Editorial content is never influenced by commercial relationships.

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