Skip to content

Besifloxacin

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

Besifloxacin is a topical fluoroquinolone antibiotic designed for ophthalmic use. It works by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes essential for bacterial DNA replication. This medication is prescribed to treat bacterial conjunctivitis (pink eye) caused by susceptible strains of bacteria.

Quick summary

Besifloxacin is an eye drop antibiotic used to treat bacterial conjunctivitis by killing susceptible bacteria.

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

Key facts at a glance

ATC
S01AE08
RxNorm
819911
Generic
Besifloxacin
Class
atc-s01
Brands
Besivance
Availability
rx
Lactation
unknown
Routes
ophthalmic
Forms
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)ophthalmic solution (eye drops)
Usual dose
1 drop
Maximum
consult physician
Frequency
3 times daily (every 6 hours)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)ophthalmic solution (eye drops)
Usual dose
1 drop
Maximum
consult physician
Frequency
3 times daily (every 6 hours)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
adult (contact lens wearers)ophthalmic solution (eye drops)
Usual dose
1 drop
Maximum
consult physician
Frequency
3 times daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity when ingested orally (approximate threshold based on fluoroquinolone class)
Chronic overdose: Not typically applicable for ophthalmic formulation; long-term topical use may cause local ocular irritation
Immediate actions
For ocular exposure: flush eyes with copious amounts of water; For ingestion: gastric lavage if within 1-2 hours, activated charcoal
Antidote
No specific antidote; supportive care(Supportive care is mainstay of treatment)
Poison Control: 1-800-222-1222

Special Populations

8 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks, topical ophthalmic use results in minimal systemic absorption

Monitor

regular prenatal monitoring if used

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if clearly needed, benefits must outweigh potential risks

Monitor

standard prenatal care

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh risks

Monitor

fetal monitoring as needed

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

consider temporarily discontinuing breastfeeding or using alternative therapy, minimal systemic absorption with topical use

Monitor

monitor infant for any adverse effects

Use with caution and monitor for adverse effects.

✓

pediatric_age

infants 1 year and older
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

approved for use in pediatric patients 1 year and older for bacterial conjunctivitis

Monitor

standard pediatric eye examination

✓

geriatric

elderly 65 years and older
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

no specific dosage adjustment required for elderly patients

Monitor

routine ophthalmologic monitoring

✓

renal_impairment

mild to moderate
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

no dosage adjustment required due to minimal systemic absorption

Monitor

standard renal function monitoring

✓

hepatic_impairment

mild to moderate
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

no dosage adjustment required due to minimal systemic absorption

Monitor

standard liver function monitoring

Statistics and clinical data

prescribingFDA
2023

FDA Approval Year

Value:2009

FDA approval for Besifloxacin ophthalmic suspension 0.6% for treatment of bacterial conjunctivitis

drug_classFDA
2023

Drug class

Value:Fluoroquinolone antibiotic

Antimicrobial class information

usageFDA
2023

Indication

Value:Bacterial conjunctivitis

FDA-approved therapeutic indication

formulationFDA
2023

Dosage form

Value:Ophthalmic suspension 0.6%

Topical ophthalmic formulation

Besifloxacin ophthalmic suspension is indicated for the treatment of bacterial conjunctivitis caused by susceptible strains of organisms including Haemophilus influenzae, Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus mitis group, and Streptococcus pneumoniae.

Besifloxacin is a fluoroquinolone that exerts its antibacterial effect by inhibiting two key bacterial enzymes: DNA gyrase and topoisomerase IV. These enzymes are essential for bacterial DNA replication, transcription, repair, and recombination. By blocking these enzymes, besifloxacin prevents bacterial growth and allows the body's immune system to eliminate the infection.

Besifloxacin is for topical ophthalmic use only and should not be injected into the eye. Patients should wash hands before application and avoid contaminating the tip of the bottle. Contact lenses should not be worn during treatment of infectious conjunctivitis. Common side effects may include eye redness, discomfort, and blurred vision. As with all fluoroquinolones, allergic reactions can occur.

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