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Apomorphine

Published: July 26, 2026Updated: August 27, 2026

Apomorphine is a dopamine agonist primarily used to treat advanced Parkinson's disease, specifically for managing sudden 'off' episodes where motor symptoms return despite other medications. It provides rapid relief when given as a subcutaneous injection, making it useful when oral medications alone are insufficient.

Quick summary

Apomorphine is a fast-acting dopamine agonist injection for treating Parkinson's disease 'off' episodes.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 27, 2026Editorial policy
BOXED WARNING

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
N04BC07
RxNorm
17767
Generic
Apomorphine
Class
atc-g04
Brands
Kynmobi, Onapgo, Apokyn
Availability
otc
Pregnancy
C
Lactation
caution
Half-life (h)
0.7
Onset (min)
15
Duration (h)
1
Routes
sublingual, subcutaneous, intramuscular
Forms
sublingual film, injection solution, infusion solution
Regions
United States, European Union, Canada, United Kingdom, Australia
Monitoring
orthostatic blood pressure, QT interval, nausea and vomiting, daytime somnolence, impulse control

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)sublingual film
Usual dose
2mg to 10mg as needed
Maximum
consult physician
Frequency
up to 5 times daily (for 'off' episodes)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (not applicable)not established
Usual dose
not recommended
Maximum
consult physician
Frequency
not applicable
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)sublingual film
Usual dose
2mg to 8mg as needed
Maximum
consult physician
Frequency
up to 5 times daily (use with caution)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity - doses above 100mg associated with severe adverse effects
Chronic overdose: Prolonged use at supratherapeutic doses may lead to cumulative toxicity affecting cardiovascular and central nervous systems
Immediate actions
Supportive care - maintain airway, intravenous fluids for hypotension, cardiac monitoring, consider gastric lavage if within 1 hour of ingestion
Antidote
No specific antidote exists(Treatment is supportive; no specific antidote has been proven effective)
Poison Control: 1-800-222-1222

Special Populations

8 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring

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

✗

pregnancy

second trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring and growth assessments

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring and uterine activity monitoring

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

✗

lactation

breastfeeding
contraindicated
FDA Category
C
Dose Adjustment

not applicable

Key Recommendations

do not breastfeed during apomorphine treatment; discontinue breastfeeding or discontinue drug

Monitor

not applicable

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

start at lower end of dosing range

Key Recommendations

use with caution due to increased sensitivity to side effects; monitor for orthostatic hypotension and sedation

Monitor

regular monitoring of blood pressure, cardiac function, and adverse effects

Use with caution and monitor for adverse effects.

✗

pediatric_age

children adolescents
contraindicated
FDA Category
N
Dose Adjustment

not applicable

Key Recommendations

not recommended for use in pediatric populations; safety and efficacy not established

Monitor

not applicable

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

⚠

renal_impairment

moderate
caution
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with caution; dose reduction recommended; monitor renal function

Monitor

monitor renal function and adjust dose based on response and tolerability

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

use with caution; no specific dose adjustment established; monitor hepatic function

Monitor

monitor liver function tests and for signs of hepatotoxicity

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

First FDA approval

Value:2004

Apokyn injection approved for Parkinson's disease

drug_classWHO
2023

Drug class

Value:Dopamine agonist

Non-selective dopamine receptor agonist

usageFDA
2023

Primary indication

Value:Treatment of 'off' episodes in Parkinson's disease

Acute, intermittent treatment of hypomobility

administrationFDA
2023

Route of administration

Value:Sublingual film, subcutaneous injection

Kynmobi (sublingual), Apokyn (injection)

Apomorphine is used to treat hypomobility ('off') episodes in patients with advanced Parkinson's disease who are already receiving levodopa and other dopaminergic medications. It may also be used diagnostically to assess dopamine responsiveness in movement disorders.

As a non-ergot dopamine agonist, apomorphine stimulates D1 and D2 dopamine receptors in the brain, compensating for reduced dopamine levels in Parkinson's disease and restoring motor function during 'off' periods.

Apomorphine causes significant nausea, so antiemetics (typically domperidone) are co-prescribed. It requires careful dose titration and monitoring. Subcutaneous administration via injection or pump is used. It should not be given intravenously. Patients should be counseled on injection technique, potential orthostatic hypotension, and rare impulse control issues.

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 27, 2026. · Read our editorial policy