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Apraclonidine

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

Apraclonidine is an ophthalmic alpha-2 adrenergic agonist used to lower elevated intraocular pressure in conditions such as open-angle glaucoma and ocular hypertension. It is available as eye drops and is used for long-term pressure management as well as short-term control of pressure spikes following laser eye procedures.

Quick summary

Apraclonidine is an eye pressure-lowering medication used to treat glaucoma and control intraocular pressure after eye surgery.

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

Key facts at a glance

ATC
S01EA03
RxNorm
14845
Generic
Apraclonidine
Class
atc-s01
Brands
Iopidine
Availability
rx
Lactation
unknown
Routes
ophthalmic
Forms
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: Ingestion of approximately 5ml or more of 1% apraclonidine solution (containing 50mg or more) may cause serious systemic toxicity in adults
Chronic overdose: Prolonged use leading to systemic absorption may result in cumulative cardiovascular effects including hypotension and bradycardia
Immediate actions
Supportive care including intravenous fluids, vasopressors if needed, continuous cardiac monitoring, activated charcoal within 1 hour of ingestion if patient is conscious
Antidote
No specific antidote exists; treatment is supportive and symptomatic(N/A - no antidote available, supportive care is the mainstay of treatment)
Poison Control: 1-800-222-1222

Special Populations

8 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh risks to fetus

Monitor

fetal growth monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use close to delivery due to potential effects on newborn

Monitor

neonatal monitoring after birth

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

consider temporarily discontinuing breastfeeding or using alternative therapy

Monitor

monitor infant for drowsiness and lethargy

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

start at lowest effective dose

Key Recommendations

monitor for systemic absorption and cardiovascular effects

Monitor

regular blood pressure and heart rate monitoring

Use with caution and monitor for adverse effects.

✗

pediatric_age

children under 12
unsafe
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

avoid use in pediatric patients due to limited safety data

Monitor

not applicable

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

⚠

renal_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

no adjustment typically required

Key Recommendations

use with caution due to minimal systemic absorption from ophthalmic formulation

Monitor

monitor for systemic effects

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

no adjustment typically required

Key Recommendations

use with caution due to limited systemic absorption from ophthalmic formulation

Monitor

monitor for systemic effects

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1990

FDA approval for ocular use

drug_classWHO
2023

Drug class

Value:Alpha-2 adrenergic agonist

Pharmacological classification

usageMedical guidelines
2023

Primary indication

Value:Control of intraocular pressure

Primary therapeutic use

mechanismFDA
2023

Mechanism of action

Value:Reduces aqueous humor production

Pharmacological mechanism

Apraclonidine treats elevated intraocular pressure associated with open-angle glaucoma and ocular hypertension. It is also used to control acute intraocular pressure elevations following laser eye surgeries, such as LASIK, photocoagulation, or iridotomy.

As a selective alpha-2 adrenergic agonist, apraclonidine reduces aqueous humor production in the ciliary body of the eye, which decreases intraocular pressure. It may also slightly increase uveoscleral outflow of fluid.

Common side effects include eye redness, burning, itching, dryness, and drowsiness. It should be used cautiously in patients with cardiovascular disease, depression, or those taking MAO inhibitors. Not recommended for use in children due to reported CNS effects. May lose effectiveness over time (tachyphylaxis) with chronic use.

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