Skip to content

Meperidine

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

Meperidine is a synthetic opioid analgesic used to treat moderate to severe pain. It works by binding to opioid receptors in the brain and spinal cord to reduce pain perception and produce sedation.

Quick summary

Meperidine is a short-acting opioid pain medication prescribed for acute, severe pain when other treatments are inadequate.

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
N02AB02
RxNorm
6754
Generic
Meperidine
Class
atc-n02
Brands
Demerol
Availability
rx
Lactation
unknown
Routes
oral
Forms
injection, prefilled syringe, solution, tablet, 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
50-150mg every 3-4 hours as needed
Maximum
consult physician
Frequency
every 3-4 hours PRN
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
1-1.5 mg/kg/dose every 3-4 hours as needed
Maximum
consult physician
Frequency
every 3-4 hours PRN
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
25-50mg every 3-4 hours as needed
Maximum
consult physician
Frequency
every 3-4 hours PRN
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Doses exceeding 1000mg may cause serious toxicity, with respiratory depression being the primary concern
Chronic overdose: Accumulation of normeperidine metabolite with repeated dosing, particularly in patients with renal impairment
Immediate actions
Secure airway and provide ventilatory support, administer naloxone, establish IV access, monitor vital signs continuously, consider gastric decontamination if ingestion was recent
Antidote
Naloxone(Highly effective in reversing opioid effects within minutes; may require repeated dosing due to meperidine's longer half-life compared to naloxone)
Poison Control: 1-800-222-1222

Special Populations

14 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; meperidine crosses the placenta

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

use only if benefits clearly outweigh risks; consider alternative analgesics

Monitor

fetal heart rate monitoring

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 near delivery; can cause prolonged neonatal respiratory depression

Monitor

intensive fetal and neonatal monitoring

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

✗

pediatric_age

neonates
contraindicated
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

avoid in neonates due to immature hepatic metabolism and increased risk of respiratory depression

Monitor

continuous respiratory and cardiac monitoring

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

✗

pediatric_age

pediatric under 6 months
unsafe
FDA Category
C
Dose Adjustment

avoid or use with extreme caution at reduced doses

Key Recommendations

use only in monitored setting; not recommended for repeated dosing due to normeperidine accumulation

Monitor

close respiratory and neurological monitoring

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

⚠

pediatric_age

pediatric 6 months to 12 years
caution
FDA Category
C
Dose Adjustment

reduce dose based on weight; use lowest effective dose

Key Recommendations

avoid repeated dosing due to normeperidine accumulation; single dose or short-term use only

Monitor

monitor for respiratory depression and sedation

Use with caution and monitor for adverse effects.

⚠

geriatric

geriatric 65 plus
caution
FDA Category
C
Dose Adjustment

reduce initial dose by 25-50%

Key Recommendations

use lowest effective dose for shortest duration; increased sensitivity to CNS effects

Monitor

monitor for sedation, respiratory depression, confusion, and falls

Use with caution and monitor for adverse effects.

✗

renal_impairment

severe renal impairment
contraindicated
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

meperidine is contraindicated in severe renal impairment due to normeperidine accumulation

Monitor

not applicable - avoid use

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

✗

renal_impairment

moderate renal impairment
unsafe
FDA Category
C
Dose Adjustment

avoid if possible; if must use, reduce dose significantly and limit to single dose

Key Recommendations

avoid repeated dosing; normeperidine accumulates and is not dialyzable

Monitor

monitor for signs of neurotoxicity, seizures, and respiratory depression

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

⚠

renal_impairment

mild renal impairment
caution
FDA Category
C
Dose Adjustment

reduce dose and extend dosing interval

Key Recommendations

use with caution; avoid repeated dosing; monitor renal function

Monitor

monitor for normeperidine accumulation and neurotoxicity

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

severe hepatic impairment
unsafe
FDA Category
C
Dose Adjustment

avoid if possible; if used, reduce dose significantly

Key Recommendations

impaired metabolism leads to prolonged half-life and increased bioavailability

Monitor

close monitoring for respiratory depression and prolonged sedation

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

⚠

hepatic_impairment

moderate hepatic impairment
caution
FDA Category
C
Dose Adjustment

reduce dose by 50%

Key Recommendations

use with caution; may require dose reduction and extended dosing intervals

Monitor

monitor for excessive sedation and respiratory depression

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild hepatic impairment
caution
FDA Category
C
Dose Adjustment

may require slight dose reduction

Key Recommendations

use with caution; monitor response

Monitor

standard monitoring for opioid effects

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

meperidine is excreted in breast milk; avoid during breastfeeding

Monitor

not applicable - avoid use

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

Statistics and clinical data

prescribingFDA
2023

Commonly prescribed since

Value:1950s

General prescribing information

drug_classWHO
2023

Drug class

Value:Opioid analgesic

Drug class information

usageMedical guidelines
2023

Common uses

Value:Moderate to severe pain management

Common therapeutic uses

regulationDEA
2023

Controlled substance schedule

Value:Schedule II

Regulatory classification

Treatment of acute, moderate to severe pain (e.g., preoperative medication, obstetric analgesia, post-operative pain). Due to its metabolite normeperidine, it is generally limited to short-term use (less than 48 hours) and not recommended for chronic pain management.

Meperidine is a full opioid agonist that binds primarily to mu-opioid receptors in the central nervous system. This interaction inhibits ascending pain pathways, altering the perception and emotional response to pain while also producing sedative effects.

High risk of dependence, abuse, and misuse. Contraindicated with MAOIs and in patients with severe respiratory depression. The metabolite normeperidine accumulates with repeated dosing, increasing risk of neurotoxicity (seizures). Not preferred for pain management due to unfavorable safety profile compared to other opioids. May cause serotonin syndrome when combined with serotonergic drugs.

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 July 26, 2026. · Read our editorial policy