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Bezafibrate

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

Bezafibrate is a lipid-lowering medication belonging to the fibrate class, used to treat elevated cholesterol and triglyceride levels. It is primarily prescribed for patients with hypertriglyceridemia and mixed dyslipidemia who have not responded adequately to diet and exercise modifications. The medication works by activating specific receptors in the liver to reduce fatty acid production and enhance the breakdown of lipid particles in the blood.

Quick summary

Bezafibrate is a fibrate medication used to lower elevated triglycerides and cholesterol levels in patients with lipid disorders.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 2026Editorial policy

Key facts at a glance

ATC
C10AB02
RxNorm
1525
Generic
Bezafibrate
Class
atc-c10
Brands
—
Availability
rx
Lactation
unknown
Routes
oral
Forms
tablet
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: Doses above 6 grams may cause significant toxicity
Chronic overdose: prolonged use at high doses may lead to cumulative toxicity
Immediate actions
gastric lavage if within 1-2 hours, activated charcoal, supportive care
Antidote
no specific antidote(treatment is supportive and symptomatic)
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, consider discontinuation before conception

Monitor

regular fetal monitoring and ultrasound assessments

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

discontinue use

Key Recommendations

discontinue before third trimester due to potential risk of bleeding in mother and fetus

Monitor

fetal well-being monitoring

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

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

avoid

Key Recommendations

do not breastfeed while taking bezafibrate, discontinue drug or stop breastfeeding

Monitor

monitor infant for any adverse effects if exposure occurs

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 dose

Key Recommendations

start with reduced dose and monitor renal function closely, consider age-related decline in renal and hepatic function

Monitor

regular renal function monitoring, liver enzyme checks, and lipid panel assessment

Use with caution and monitor for adverse effects.

?

pediatric_age

children adolescents
unknown
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

not recommended for use in children and adolescents due to limited safety and efficacy data

Monitor

no established monitoring protocol for pediatric population

⚠

renal_impairment

mild moderate
caution
FDA Category
N
Dose Adjustment

dose reduction required

Key Recommendations

reduce dose to 200mg daily in mild renal impairment, avoid in moderate impairment or reduce to 200mg every other day

Monitor

monitor serum creatinine and calculate creatinine clearance regularly, monitor for muscle-related adverse effects

Use with caution and monitor for adverse effects.

✗

renal_impairment

severe
contraindicated
FDA Category
N
Dose Adjustment

avoid use

Key Recommendations

contraindicated in patients with severe renal impairment (creatinine clearance <30 mL/min)

Monitor

regular renal function monitoring if used off-label

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

contraindicated in severe hepatic impairment due to metabolism in liver

Monitor

liver function tests before and during treatment

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

Statistics and clinical data

prescribingEMA
2023

Commonly prescribed since

Value:1980s

General prescribing information bezafibrate has been available since the 1980s in Europe

Drug classWHO
2023

Value:Fibrate/PPAR-alpha agonist

Bezafibrate belongs to the fibrate class of lipid-lowering medications and is a peroxisome proliferator-activated receptor alpha (PPAR-alpha) agonist

usageMedical guidelines
2023

Common uses

Value:Hyperlipidemia, Hypertriglyceridemia, Mixed dyslipidemia

Bezafibrate is primarily used to treat elevated cholesterol and triglyceride levels

mechanismFDA
2023

Mechanism of action

Value:PPAR-alpha activation increases HDL cholesterol and reduces triglycerides

Pharmacological mechanism of bezafibrate

Bezafibrate is indicated for the treatment of hypertriglyceridemia and mixed dyslipidemia when dietary measures alone are insufficient. It is particularly effective at lowering elevated triglyceride levels and may provide modest improvements in LDL cholesterol and HDL cholesterol levels.

Bezafibrate works by activating peroxisome proliferator-activated receptor alpha (PPAR-α) in liver cells. This activation increases the activity of lipoprotein lipase, enhances fatty acid oxidation, and reduces the production of very-low-density lipoprotein (VLDL) by the liver, ultimately leading to decreased circulating triglyceride levels.

Bezafibrate is typically taken 2-3 times daily with meals. Common side effects may include gastrointestinal symptoms, muscle pain, and elevated liver enzymes. Patients should report unexplained muscle pain, tenderness, or weakness, as fibrates can rarely cause muscle-related complications. Regular monitoring of lipid panels and liver function is recommended during treatment.

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