ZYMAXID™ (gatifloxacin ophthalmic solution) 0.5%
(description)
HIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use ZYMAXID™ safely and effectively. See full prescribing information for ZYMAXID™. ZYMAXID™ (gatifloxacin ophthalmic solution) 0.5% DESCRIPTION ZYMAXID™ sterile ophthalmic solution is an 8-methoxyfluoroquinolone anti-infective for the treatment of bacterial conjunctivitis. Its chemical name is (±)-1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid, sesquihydrate. ZYMAXID™ is a clear, pale yellow, sterile, preserved aqueous solution with an osmolality of 260-330 mOsm/kg and a pH of 5.1-5.7. ZYMAXID™ contains Active: gatifloxacin 0.5% (5 mg/mL); Inactives: benzalkonium chloride 0.005%; edetate disodium; purified water; and sodium chloride. May contain hydrochloric acid and/or sodium hydroxide to adjust pH. |
Clinical pharmacology
Mechanism of Action Gatifloxacin is a fluoroquinolone antibacterial. Pharmacokinetics Microbiology Resistance to gatifloxacin in vitro develops via multiple-step mutations. Resistance to gatifloxacin in vitro occurs at a general frequency of 1 x 10-7 to 10-10. Gatifloxacin has been shown to be active against most isolates of the following organisms both microbiologically and clinically, in conjunctival infections as described in the INDICATIONS AND USAGE. Aerobic Gram-Positive Bacteria: Aerobic Gram-Negative Bacteria: *Efficacy for this organism was studied in fewer than 10 infections. |
Indications and usage
INDICATIONS AND USAGE
ZYMAXID™ ophthalmic solution is a topical fluoroquinolone anti-infective indicated for the treatment of bacterial conjunctivitis caused by susceptible strains of the following organisms: Haemophilus influenzae, Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus mitis group*, Streptococcus oralis*, Streptococcus pneumoniae *Efficacy for this organism was studied in fewer than 10 infections. |
Precautions
WARNINGS AND PRECAUTIONS Topical Ophthalmic Use Only Growth of Resistant Organisms with Prolonged Use 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 ZYMAXID™ |
Adverse reactions
ADVERSE REACTIONS
Most common adverse reactions occurring in >/= 1 % of patients included worsening of conjunctivitis, eye irritation, dysgeusia, and eye pain. To report SUSPECTED ADVERSE REACTIONS, contact Allergan at 1-800-433-8871 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. |
Dosage and administration
DOSAGE AND ADMINISTRATION
Patients 1 year of age or older: Instill one drop every two hours in the affected eye(s) while awake, up to 8 times on Day 1. Instill one drop two to four times daily in the affected eye(s) while awake on Days 2 through 7. |
Reference(s)
National Institutes of Health, U.S. National Library of Medicine, DailyMed Database.
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