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Hydromorphone

Published: July 26, 2026Updated: July 26, 2026

Hydromorphone is a potent opioid analgesic used to manage moderate to severe pain when other treatments are insufficient. As a full mu-opioid receptor agonist, it provides powerful pain relief without a ceiling effect, meaning dose increases can continue to provide additional analgesia. It is available in various formulations including immediate and extended-release versions for different pain management needs.

Quick summary

Hydromorphone is a strong opioid pain medication used for moderate to severe pain relief.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 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
N02AA03
RxNorm
3423
Generic
Hydromorphone
Class
atc-n02
Brands
Dilaudid, Dilaudid Cough
Availability
rx
Lactation
unknown
Routes
oral, rectal
Forms
prefilled syringe, injection, capsule, tablet, 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: Single dose above 25mg may cause serious toxicity in opioid-naive individuals
Chronic overdose: Repeated use leading to accumulation, especially in patients with renal impairment
Immediate actions
Ensure airway patency, provide ventilatory support, administer naloxone, monitor vital signs
Antidote
Naloxone(Minutes to hours depending on formulation)
Poison Control: 1-800-222-1222

Special Populations

13 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; opioid analgesics should not be used in early pregnancy

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 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 especially near delivery; may cause neonatal respiratory depression and withdrawal

Monitor

close fetal monitoring; neonatal assessment for withdrawal symptoms

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

✗

lactation

breastfeeding
contraindicated
FDA Category
C
Dose Adjustment

discontinue breastfeeding

Key Recommendations

hydromorphone passes into breast milk; do not breastfeed during treatment

Monitor

monitor infant for signs of sedation or respiratory depression

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

start with 25-50% of adult dose

Key Recommendations

use lowest effective dose; increased sensitivity to opioid effects; monitor for falls and constipation

Monitor

close monitoring of respiratory status, cognitive function, and bowel function

Use with caution and monitor for adverse effects.

✗

pediatric_age

children under 12
contraindicated
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

hydromorphone is not recommended for use in children, especially for cough

Monitor

not applicable

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

⚠

pediatric_age

adolescents 12 17
caution
FDA Category
C
Dose Adjustment

use with extreme caution and reduced dosing

Key Recommendations

use only for severe pain; not recommended for cough; monitor closely for respiratory depression

Monitor

close monitoring of respiratory status

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild
caution
FDA Category
N
Dose Adjustment

reduce dose by 25%

Key Recommendations

use with caution; monitor for accumulation

Monitor

monitor renal function and drug levels

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate
caution
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with caution; extended intervals between doses

Monitor

frequent monitoring of renal function and drug levels

Use with caution and monitor for adverse effects.

✗

renal_impairment

severe
unsafe
FDA Category
N
Dose Adjustment

avoid or use with great caution

Key Recommendations

avoid if possible; if used, significantly reduce dose and extend dosing interval

Monitor

very close monitoring of renal function, drug levels, and respiratory status

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

⚠

hepatic_impairment

mild
caution
FDA Category
N
Dose Adjustment

reduce initial dose by 25%

Key Recommendations

use with caution; metabolism may be reduced

Monitor

monitor liver function and drug response

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

moderate
unsafe
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with extreme caution; significant metabolism impairment

Monitor

close monitoring of liver function and respiratory status

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

✗

hepatic_impairment

severe
contraindicated
FDA Category
N
Dose Adjustment

avoid use

Key Recommendations

do not use in severe hepatic impairment

Monitor

not applicable

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

Statistics and clinical data

prescribingFDA
2023

Commonly prescribed since

Value:1990s

General prescribing information for hydromorphone

drug_classWHO
2023

Drug class

Value:Opioid analgesic

Drug class as opioid receptor agonist

usageMedical guidelines
2023

Common uses

Value:Management of pain (moderate to severe)

Primary therapeutic indication

regulatoryDEA
2023

Controlled substance schedule

Value:Schedule II

Federal controlled substance classification

Treatment of moderate to severe pain requiring opioid analgesia, including postoperative pain, cancer pain, and other acute or chronic pain conditions when non-opioid analgesics are inadequate.

Hydromorphone acts as a full agonist at mu-opioid receptors in the central nervous system, reducing pain perception and altering the emotional response to pain. It has no ceiling effect, allowing for dose escalation to achieve adequate pain control.

High risk of dependence, tolerance, and addiction with prolonged use. Can cause respiratory depression, especially at high doses or when combined with CNS depressants. Schedule II controlled substance with strict prescribing regulations. Dosage must be individualized and carefully titrated to balance pain relief with safety.

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 July 26, 2026. · Read our editorial policy