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Midazolam

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

Midazolam is a short-acting benzodiazepine medication commonly used for sedation, anxiety relief, and amnesia during medical procedures. It works by enhancing the effects of GABA, a calming neurotransmitter in the brain, making it valuable for preoperative sedation, anesthesia induction, and critical care settings.

Quick summary

Midazolam is a benzodiazepine sedative used for procedural sedation, anesthesia, and seizure management.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 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
N05CD08
RxNorm
6960
Generic
Midazolam
Class
atc-n05
Brands
Nayzilam
Availability
rx
Lactation
unknown
Routes
oral, nasal
Forms
injection, prefilled syringe, solution, tablet, spray
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
5mg
Maximum
consult physician
Frequency
single dose for acute seizure
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
2.5mg
Maximum
consult physician
Frequency
single dose for acute seizure
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
2.5mg
Maximum
consult physician
Frequency
single dose for acute seizure
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious CNS depression and respiratory compromise
Chronic overdose: Prolonged use leading to accumulation and excessive sedation
Immediate actions
Maintain airway, provide ventilatory support, consider activated charcoal if early
Antidote
Flumazenil(Effective in reversing benzodiazepine sedation but must be used cautiously)
Poison Control: 1-800-222-1222

Special Populations

9 groups
✗

pregnancy

general
unsafe
FDA Category
D
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits significantly outweigh risks

Monitor

regular fetal monitoring and assessment of uterine activity

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

✗

pregnancy

first trimester
unsafe
FDA Category
D
Dose Adjustment

avoid

Key Recommendations

avoid use during first trimester due to increased risk of congenital malformations

Monitor

comprehensive fetal ultrasound at 18-20 weeks

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

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

use lowest effective dose

Key Recommendations

use with caution; consider pumping and discarding milk for 4-6 hours after dose

Monitor

monitor infant for excessive drowsiness and feeding difficulties

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use lowest effective dose; start with lowest dose and titrate slowly

Monitor

monitor for falls, confusion, and respiratory depression

Use with caution and monitor for adverse effects.

⚠

pediatric_age

neonates
caution
FDA Category
D
Dose Adjustment

significant dose reduction required

Key Recommendations

use only in controlled medical settings; avoid prolonged infusion

Monitor

continuous respiratory and cardiac monitoring

Use with caution and monitor for adverse effects.

⚠

pediatric_age

children 1 month to 12 years
caution
FDA Category
D
Dose Adjustment

reduce dose based on weight

Key Recommendations

use with caution; appropriate for sedation prior to procedures

Monitor

continuous monitoring of vital signs and airway patency

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use with caution; monitor for accumulation

Monitor

monitor renal function and sedation levels

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use with caution; extended elimination half-life expected

Monitor

monitor liver function and sedation levels

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild
safe
FDA Category
N
Dose Adjustment

no adjustment usually required

Key Recommendations

standard dosing with monitoring

Monitor

standard monitoring

Statistics and clinical data

drug_classWHO
2023

Drug class

Value:Benzodiazepine

Midazolam belongs to the benzodiazepine class of medications

usageFDA
2023

Common uses

Value:Sedation, anesthesia induction, seizure control, insomnia treatment

Primary therapeutic applications of Midazolam

brand_nameFDA
2020

Brand name (Nayzilam)

Value:Nayzilam (midazolam) nasal spray

Nayzilam is the FDA-approved nasal spray formulation for acute seizure treatment

regulatoryFDA
2023

FDA approval year

Value:1985 (injectable), 2020 (Nayzilam nasal)

FDA approval timeline for Midazolam formulations

Used for procedural sedation before minor surgeries and diagnostic procedures, induction and maintenance of anesthesia, management of status epilepticus, sedation in intensive care units, and treatment of severe insomnia (short-term).

Acts as a positive allosteric modulator at GABA-A receptors, enhancing the inhibitory effects of GABA neurotransmitter. This results in sedation, reduced anxiety, muscle relaxation, anterograde amnesia, and anticonvulsant effects.

Can cause respiratory depression when combined with opioids, alcohol, or other CNS depressants. Risk of dependence with prolonged use. Should only be administered by trained healthcare professionals with resuscitation equipment available. Contraindicated in severe respiratory insufficiency, acute narrow-angle glaucoma, and myasthenia gravis. May impair memory formation for the duration of action.

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