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Mirabegron

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

Mirabegron is a beta-3 adrenergic receptor agonist used to treat overactive bladder (OAB) symptoms, including urinary urgency, frequency, and urge incontinence. It works by relaxing the detrusor smooth muscle of the bladder during the storage phase, increasing bladder capacity and reducing involuntary contractions. It is an alternative to anticholinergic medications for patients who cannot tolerate anticholinergic side effects such as dry mouth and constipation.

Quick summary

Mirabegron is a bladder muscle relaxant used to treat overactive bladder symptoms by targeting beta-3 adrenergic receptors.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy

Key facts at a glance

ATC
G04BD12
RxNorm
1300786
Generic
Mirabegron
Class
atc-g04
Brands
Myrbetriq
Availability
rx
Lactation
unknown
Routes
oral
Forms
tablet, suspension
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)extended-release tablet
Usual dose
25mg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (not_indicated)extended-release tablet
Usual dose
not approved for pediatric use
Maximum
consult physician
Frequency
not applicable
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)extended-release tablet
Usual dose
25mg once 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 of 1000 mg or higher may cause serious cardiovascular and central nervous system toxicity
Chronic overdose: Prolonged use exceeding recommended 50 mg daily dose may lead to cumulative cardiovascular effects
Immediate actions
Gastric lavage within 1-2 hours of ingestion, activated charcoal administration, continuous cardiac monitoring, supportive care
Antidote
No specific antidote exists(Treatment is supportive and symptomatic; no antidote to reverse effects)
Poison Control: 1-800-222-1222

Special Populations

10 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

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
unknown
FDA Category
N
Dose Adjustment

avoid

Key Recommendations

discontinue breastfeeding or discontinue drug; decision should be made considering importance of drug to mother

Monitor

monitor infant for adverse effects

?

pediatric_age

under 18 years
unknown
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

safety and efficacy not established in patients under 18 years of age

Monitor

not applicable

⚠

geriatric

elderly over 65
caution
FDA Category
N
Dose Adjustment

no specific adjustment; start at low end of dosing range

Key Recommendations

use with caution; monitor blood pressure due to potential for increased blood pressure and cardiovascular effects

Monitor

regular blood pressure monitoring

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

reduce dose to 25mg once daily

Key Recommendations

use with caution; dose reduction recommended for severe renal impairment (CLcr 15-29 mL/min)

Monitor

monitor renal function and blood pressure

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate
caution
FDA Category
N
Dose Adjustment

no dose adjustment required but monitor

Key Recommendations

use with caution; no dose adjustment required for moderate renal impairment (CLcr 30-59 mL/min)

Monitor

monitor renal function and blood pressure

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

reduce dose to 25mg once daily

Key Recommendations

use with caution; dose reduction recommended for severe hepatic impairment (Child-Pugh Class C)

Monitor

monitor hepatic function and blood pressure

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate
caution
FDA Category
N
Dose Adjustment

no dose adjustment required but monitor

Key Recommendations

use with caution; no dose adjustment required for moderate hepatic impairment (Child-Pugh Class B)

Monitor

monitor hepatic function and blood pressure

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classFDA
2023

Drug class

Value:Beta-3 adrenergic agonist

Pharmacological classification

prescribingFDA
2023

FDA approval year

Value:2012

Regulatory approval information

usageFDA
2023

Common uses

Value:Overactive bladder, urge urinary incontinence, urinary urgency, urinary frequency

Therapeutic indications

mechanismFDA
2023

Mechanism of action

Value:Beta-3 adrenergic receptor agonist that relaxes bladder detrusor muscle

Pharmacodynamics

Treatment of overactive bladder (OAB) with symptoms of urinary urgency, frequency, and urge incontinence in adults

Selective beta-3 adrenergic receptor agonist that relaxes detrusor smooth muscle during the bladder storage phase, increasing bladder capacity and reducing involuntary bladder contractions

Use with caution in patients with hypertension (may increase blood pressure), severe uncontrolled hypertension, and those with hepatic or renal impairment. May interact with CYP2D6 and CYP3A4 substrates. Not recommended during pregnancy or breastfeeding unless clearly needed.

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