Brand Name Besiven
Type Ophthalmic Solution
Weight 0.6%
Generic Besifloxacin
Manufacturer Incepta Pharmaceuticals Ltd.

About Besiven

Besiven Ophthalmic Solution (Incepta Pharmaceuticals Ltd.) is a brand medicine containing the generic Besifloxacin .

Medical information for Besiven Ophthalmic Solution 0.6%

Uses, dosage, side effects, and safety details below apply to Besiven Ophthalmic Solution 0.6% (generic: Besifloxacin). This is general information — consult a doctor before use.

Introduction

Besiven Ophthalmic Solution 0.6% is a fourth generation fluoroquinolone-type opthalmic antibiotic for the treatment of bacterial conjunctivitis.

Uses

Besiven Ophthalmic Solution 0.6% is a fluoroquinolone antibiotic agent used for the treatment of bacterial conjunctivitis.

Treatment of bacterial conjunctivitis. Bacterial isolates that are susceptible to besifloxacin include: CDC coryneform group G; Corynebacterium pseudodiphtheriticum; Corynebacterium striatum; Haemophilus influenzae; Moraxella lacunata; Staphylococcus aureus; Staphylococcus epidermidis; Staphylococcus hominis; Staphylococcus lugdunensis; Streptococcus mitis group; Streptococcus oralis; Streptococcus pneumoniae; Streptococcus salivarius*

Associated Conditions

  • Bacterial Conjunctivitis

Pharmacodynamics

Besiven Ophthalmic Solution 0.6% tear concentrations were higher than MIC90 (minimum inhibitory concentration) values for common bacterial pathogens and sustained for 24 hours or longer. Mean residence time in the conjunctiva was 4.7 hours.

Mechanism of Action

Besiven Ophthalmic Solution 0.6% is a bactericidal fluroquinolone-type antibiotic that inhibits bacterial enzymes, DNA gyrase and topoisomerase IV. By inhibiting DNA gyrase, DNA replication, transcription, and repair is impaired. By inhibiting topoisomerase IV, decatenation during cell devision is impaired. Inhibiting these two targets also slows down development of resistance.

Absorption

Although ocular surface concentrations are high, average systemic concentrtions after three-times daily dosing was less than 0.5 ng/mL. This indicates that besifloxacin is not appreciably absorbed into the systemic and has a very low risk of systemic side effects.

Volume of Distribution

Not absorbed into the systemic

Protein Binding

None

Route of Elimination

N/A

Half Life

The average elimination half-life of besifloxacin in plasma following multiple dosing was estimated to be 7 hours.

Clearance

N/A

Toxicity

LD50, rat: >2000 mg/kg. The most common adverse reaction reported in 2% of patients treated with besifloxacin was conjunctival redness.

Food Interactions

No interactions found.

Dosage

Adults and children (1 year of age and older): Instill one drop in the affected eye(s) 3 times a day for 7 days.

Pediatric Use: The safety and effectiveness of Besiven Ophthalmic Solution 0.6% in infants below one year of age have not been established. The efficacy of Besiven Ophthalmic Solution 0.6% in treating bacterial conjunctivitis in pediatric patients one year or older has been demonstrated in controlled clinical trials.

Geriatric Use: No overall differences in safety and effectiveness have been observed between elderly and younger patients.

Medical review

Last reviewed: 24 Jul 2026

Medically reviewed by:

This is general information, not personal medical advice. Consult a doctor before taking any medicine.

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