Label: BESIVANCE- besifloxacin suspension

  • NDC Code(s): 24208-446-02, 24208-446-05
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated April 3, 2018

If you are a consumer or patient please visit this version.

  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use BESIVANCE safely and effectively. See full prescribing information for BESIVANCE.

    BESIVANCE ® (besifloxacin ophthalmic suspension) 0.6%, for topical ophthalmic use
    Initial U.S. Approval: 2009

    INDICATIONS AND USAGE

    BESIVANCE® (besifloxacin ophthalmic suspension) 0.6%, is a quinolone antimicrobial indicated for the treatment of bacterial conjunctivitis caused by susceptible isolates of the following bacteria:

    Aerococcus viridans*, CDC coryneform group G, Corynebacterium pseudodiphtheriticum*, Corynebacterium striatum*, Haemophilus influenzae, Moraxella catarrhalis*, Moraxella lacunata*, Pseudomonas aeruginosa*, Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus hominis*, Staphylococcus lugdunensis*, Staphylococcus warneri*, Streptococcus mitis group, Streptococcus oralis, Streptococcus pneumoniae, Streptococcus salivarius*

    *Efficacy for this organism was studied in fewer than 10 infections. (1)

    DOSAGE AND ADMINISTRATION

    Instill one drop in the affected eye(s) 3 times a day, 4 to 12 hours apart for 7 days. (2)

    DOSAGE FORMS AND STRENGTHS

    Ophthalmic suspension: besifloxacin 6 mg/mL (0.6%) (3)

    CONTRAINDICATIONS

    None. (4)

    WARNINGS AND PRECAUTIONS

    Not for Injection into the Eye ( 5.1)
    Growth of Resistant Organisms with Prolonged Use ( 5.2)
    Avoidance of Contact Lenses: Patients should not wear contact lenses if they have signs or symptoms of bacterial conjunctivitis or during the course of therapy with BESIVANCE. ( 5.3)

    ADVERSE REACTIONS

    The most common adverse reaction reported in 2% of patients treated with BESIVANCE was conjunctival redness. (6)

    To report SUSPECTED ADVERSE REACTIONS, contact Bausch + Lomb, a division of Valeant Pharmaceuticals North America LLC, at 1-800-321-4576 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 4/2018

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  • FULL PRESCRIBING INFORMATION: CONTENTS*
  • 1 INDICATIONS AND USAGE

    BESIVANCE ® (besifloxacin ophthalmic suspension) 0.6%, is indicated for the treatment of bacterial conjunctivitis caused by susceptible isolates of the following bacteria:

    Aerococcus viridans*

    CDC coryneform group G

    Corynebacterium pseudodiphtheriticum*

    Corynebacterium striatum*

    Haemophilus influenzae

    Moraxella catarrhalis*

    Moraxella lacunata*

    Pseudomonas aeruginosa*

    Staphylococcus aureus

    Staphylococcus epidermidis

    Staphylococcus hominis*

    Staphylococcus lugdunensis*

    Staphylococcus warneri*

    Streptococcus mitis group

    Streptococcus oralis

    Streptococcus pneumoniae

    Streptococcus salivarius*

    *Efficacy for this organism was studied in fewer than 10 infections.

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  • 2 DOSAGE AND ADMINISTRATION

    Invert closed bottle and shake once before use.

    Instill one drop in the affected eye(s) 3 times a day, 4 to 12 hours apart for 7 days.

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  • 3 DOSAGE FORMS AND STRENGTHS

    Ophthalmic suspension containing 6 mg/mL (0.6%) of besifloxacin.

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  • 4 CONTRAINDICATIONS

    None.

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  • 5 WARNINGS AND PRECAUTIONS

    5.1 Not for Injection into the Eye

    5.2 Growth of Resistant Organisms with Prolonged Use

    As with other anti-infectives, prolonged use of BESIVANCE (besifloxacin ophthalmic suspension) 0.6% may result in overgrowth of non-susceptible organisms, including fungi. If super-infection occurs, discontinue use and institute alternative therapy. Whenever clinical judgment dictates, the patient should be examined with the aid of magnification, such as slit-lamp biomicroscopy, and, where appropriate, fluorescein staining.

    5.3 Avoidance of Contact Lenses

    Patients should not wear contact lenses if they have signs or symptoms of bacterial conjunctivitis or during the course of therapy with BESIVANCE.

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  • 6 ADVERSE REACTIONS

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.

    The data described below reflect exposure to BESIVANCE in approximately 1,000 patients between 1 and 98 years old with clinical signs and symptoms of bacterial conjunctivitis.

    The most frequently reported ocular adverse reaction was conjunctival redness, reported in approximately 2% of patients.

    Other adverse reactions reported in patients receiving BESIVANCE occurring in approximately 1-2% of patients included: blurred vision, eye pain, eye irritation, eye pruritus and headache.

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  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary
    There are no available human data for the use of BESIVANCE during pregnancy to inform any drug-associated risks; however, systemic exposure to besifloxacin from ocular administration is low [see Clinical Pharmacology (12.3)].

    Oral administration of besifloxacin to pregnant rats during organogenesis or during the pre/postnatal period did not produce adverse embryofetal or offspring effects at clinically relevant systemic exposures [see Data].

    Data
    Animal Data

    In an embryofetal development study in rats, the administration of besifloxacin at oral doses up to 1,000 mg/kg/day during organogenesis was not associated with visceral or skeletal malformations in rat fetuses, although this dose was associated with maternal toxicity (reduced body weight gain and food consumption) and maternal mortality. Increased post-implantation loss, decreased fetal body weights, and decreased fetal ossification were also observed. At this dose, the mean Cmax in the rat dams was approximately 20 mcg/mL, approximately 46,500 times the mean plasma concentrations measured in humans at the recommended human ophthalmic dose (RHOD). The No Observed Adverse Effect Level (NOAEL) for this embryofetal development study was 100 mg/kg/day (Cmax, 5 mcg/mL, approximately 11,600 times the mean plasma concentrations measured in humans at the RHOD).

    In a prenatal and postnatal development study in rats, the NOAELs for both fetal/neonate and maternal toxicity were 100 mg/kg/day. At 1,000 mg/kg/day, pups weighed significantly less than controls and had a reduced neonatal survival rate. Attainment of developmental landmarks and sexual maturation was delayed, although surviving pups from this dose group that were reared to maturity did not demonstrate deficits in behavior, including activity, learning and memory, and their reproductive capacity appeared normal.

    8.2 Lactation

    Risk Summary

    There are no data on the presence of BESIVANCE in human milk, the effects on the breastfed infant, or the effects on milk production. However, systemic exposure to besifloxacin following topical ocular administration is low [see Clinical Pharmacology (12.3)], and it is not known whether measurable levels of besifloxacin would be present in maternal milk following topical ocular administration.

    The developmental and health benefits of breastfeeding should be considered, along with the mother’s clinical need for BESIVANCE, and any potential adverse effects on the breastfed infant from BESIVANCE.

    8.4 Pediatric Use

    The safety and effectiveness of BESIVANCE in infants below one year of age have not been established. The efficacy of BESIVANCE in treating bacterial conjunctivitis in pediatric patients one year or older has been demonstrated in controlled clinical trials [see Clinical Studies (14)].

    There is no evidence that the ophthalmic administration of quinolones has any effect on weight bearing joints, even though systemic administration of some quinolones has been shown to cause arthropathy in immature animals.

    8.5 Geriatric Use

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

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  • 11 DESCRIPTION

    BESIVANCE® (besifloxacin ophthalmic suspension) 0.6%, is a sterile ophthalmic suspension of besifloxacin formulated with DuraSite®† (polycarbophil, edetate disodium dihydrate and sodium chloride). Each mL of BESIVANCE contains 6.63 mg besifloxacin hydrochloride equivalent to 6 mg besifloxacin base. It is an 8-chloro fluoroquinolone anti-infective for topical ophthalmic use.

    Besifloxacin hydrochloride structural formula

    C19H21ClFN3O3•HCl

    Molecular Weight 430.30

    Chemical Name: (+)-7-[(3R)-3-aminohexahydro-1H-azepin-1-yl]-8-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid hydrochloride.

    Besifloxacin hydrochloride is a white to pale yellowish-white powder.

    Each mL contains:

    Active: besifloxacin 0.6% (6 mg/mL);

    Inactives: polycarbophil, mannitol, poloxamer 407, sodium chloride, edetate disodium dihydrate, sodium hydroxide and water for injection.

    Preservative: benzalkonium chloride 0.01%

    BESIVANCE is an isotonic suspension with an osmolality of approximately 290 mOsm/kg.

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  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Besifloxacin is a fluoroquinolone antibacterial [see Microbiology (12.4)].

    12.3 Pharmacokinetics

    Plasma concentrations of besifloxacin were measured in adult patients with suspected bacterial conjunctivitis who received BESIVANCE bilaterally three times a day (16 doses total). Following the first and last dose, the maximum plasma besifloxacin concentration in each patient was less than 1.3 ng/mL. The mean besifloxacin Cmax was 0.37 ng/mL on day 1 and 0.43 ng/mL on day 6. The average elimination half-life of besifloxacin in plasma following multiple dosing was estimated to be 7 hours.

    12.4 Microbiology

    Besifloxacin is an 8-chloro fluoroquinolone with an N-1 cyclopropyl group. The compound has activity against Gram-positive and Gram-negative bacteria due to the inhibition of both bacterial DNA gyrase and topoisomerase IV. DNA gyrase is an essential enzyme required for replication, transcription and repair of bacterial DNA. Topoisomerase IV is an essential enzyme required for partitioning of the chromosomal DNA during bacterial cell division. Besifloxacin is bactericidal with minimum bactericidal concentrations (MBCs) generally within one dilution of the minimum inhibitory concentrations (MICs).

    The mechanism of action of fluoroquinolones, including besifloxacin, is different from that of aminoglycoside, macrolide, and β-lactam antibiotics. Therefore, besifloxacin may be active against pathogens that are resistant to these antibiotics and these antibiotics may be active against pathogens that are resistant to besifloxacin. In vitro studies demonstrated cross-resistance between besifloxacin and some fluoroquinolones.

    In vitro resistance to besifloxacin develops via multiple-step mutations and occurs at a general frequency of < 3.3 x 10-10 for Staphylococcus aureus and < 7 x 10-10 for Streptococcus pneumoniae.

    Besifloxacin has been shown to be active against most isolates of the following bacteria both in vitro and in conjunctival infections treated in clinical trials [see Indications and Usage (1)]:

     
    Aerococcus viridans*
     
    CDC coryneform group G
     
    Corynebacterium pseudodiphtheriticum*
     
    Corynebacterium striatum*
     
    Haemophilus influenzae
     
    Moraxella catarrhalis*
     
    Moraxella lacunata*
     
    Pseudomonas aeruginosa*
     
    Staphylococcus aureus
     
    Staphylococcus epidermidis
     
    Staphylococcus hominis*
     
    Staphylococcus lugdunensis*
     
    Staphylococcus warneri*
     
    Streptococcus mitis group
     
    Streptococcus oralis
     
    Streptococcus pneumoniae
     
    Streptococcus salivarius*
     
    *Efficacy for this organism was studied in fewer than 10 infections.
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  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Long-term studies in animals to determine the carcinogenic potential of besifloxacin have not been performed.

    No in vitro mutagenic activity of besifloxacin was observed in an Ames test (up to 3.33 mcg/plate) on bacterial tester strains Salmonella typhimurium TA98, TA100, TA1535, TA1537 and Escherichia coli WP2uvrA. However, it was mutagenic in S. typhimurium strain TA102 and E. coli strain WP2 (pKM101). Positive responses in these strains have been observed with other quinolones and are likely related to topoisomerase inhibition.

    Besifloxacin induced chromosomal aberrations in CHO cells in vitro and it was positive in an in vivo mouse micronucleus assay at oral doses ≥1,500 mg/kg. Besifloxacin did not induce unscheduled DNA synthesis in hepatocytes cultured from rats given the test compound up to 2,000 mg/kg by the oral route. In a fertility and early embryonic development study in rats, besifloxacin did not impair the fertility of male or female rats at oral doses of up to 500 mg/kg/day. This dose is approximately 26,500 times higher than the mean plasma concentration measured in humans at the recommended human ophthalmic dose.

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  • 14 CLINICAL STUDIES

    In a randomized, double-masked, vehicle-controlled, multicenter clinical trial, in which patients 1-98 years of age were dosed 3 times a day for 5 days, BESIVANCE was superior to its vehicle in patients with bacterial conjunctivitis. Clinical resolution was achieved in 45% (90/198) for the BESIVANCE-treated group versus 33% (63/191) for the vehicle-treated group (difference 12%, 95% CI 3% - 22%). Microbiological outcomes demonstrated a statistically significant eradication rate for causative pathogens of 91% (181/198) for the BESIVANCE-treated group versus 60% (114/191) for the vehicle-treated group (difference 31%, 95% CI 23% - 40%). Microbiologic eradication does not always correlate with clinical outcome in anti-infective trials.

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  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    BESIVANCE® (besifloxacin ophthalmic suspension) 0.6%, is supplied as a sterile ophthalmic suspension in a white low density polyethylene (LDPE) bottle with a controlled dropper tip and tan polypropylene cap. Tamper evidence is provided with a shrink band around the cap and neck area of the package.

    5 mL in 7.5 mL bottle
    NDC 24208-446-05


    Storage: Store at 15°- 25°C (59°- 77°F). Protect from light.

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  • 17 PATIENT COUNSELING INFORMATION

    Handling the Container

    Advise patients to avoid contaminating the applicator tip with material from the eye, fingers or other source.

    Use with Contact Lenses

    Advise patients not to wear contact lenses if they have signs or symptoms of bacterial conjunctivitis or during the course of therapy with BESIVANCE.

    Dosing Instructions

    Patients should be instructed to invert closed bottle (upside down) and shake once before each use.

    Distributed by:

    Bausch + Lomb, a division of

    Valeant Pharmaceuticals North America LLC

    Bridgewater, NJ 08807 USA

    U.S. Patent Numbers: 6,685,958; 6,699,492; 8,415,342; 8,481,526; 8,604,020 and 8,937,062

    Besivance is a trademark of Bausch & Lomb Incorporated or its affiliates. All other product/brand names and/or logos are trademarks of their respective owners.

    © Bausch & Lomb Incorporated

    DuraSite is a trademark of InSite Vision Incorporated.

    9142707(folded)

    9142607(flat)

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  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    carton.jpg

    NDC 24208-446-05

    BAUSCH + LOMB

    Besivance®

    besifloxacin ophthalmic

    suspension, 0.6%

    Rx only
    Sterile

    FOR OPHTHALMIC

    USE ONLY.

    5 mL

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  • INGREDIENTS AND APPEARANCE
    BESIVANCE 
    besifloxacin suspension
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:24208-446
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BESIFLOXACIN (UNII: BFE2NBZ7NX) (BESIFLOXACIN - UNII:BFE2NBZ7NX) BESIFLOXACIN 6 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    POLYCARBOPHIL (UNII: W25LM17A4W)  
    MANNITOL (UNII: 3OWL53L36A)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:24208-446-05 1 in 1 CARTON 05/28/2009
    1 5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2 NDC:24208-446-02 1 in 1 CARTON 05/28/2009
    2 2 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA022308 05/28/2009
    Labeler - Bausch & Lomb Incorporated (196603781)
    Establishment
    Name Address ID/FEI Business Operations
    Bausch & Lomb Incorporated 079587625 MANUFACTURE(24208-446) , LABEL(24208-446) , PACK(24208-446)
    Establishment
    Name Address ID/FEI Business Operations
    Quality Packaging Specialists International, LLC 078440982 LABEL(24208-446) , PACK(24208-446)
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