Product Elements:
Ofloxacin ofloxacin ofloxacin ofloxacin sodium chloride water hydrochloric acid sodium hydroxide benzalkonium chloride
Drug Interactions:
Drug interactions: specific drug interaction studies have not been conducted with ofloxacin ophthalmic solution. however, the systemic administration of some quinolones has been shown to elevate plasma concentrations of theophylline, interfere with the metabolism of caffeine, and enhance the effects of the oral anticoagulant warfarin and its derivatives, and has been associated with transient elevations in serum creatinine in patients receiving cyclosporine concomitantly.
Indications and Usage:
Indications and usage ofloxacin ophthalmic solution is indicated for the treatment of infections caused by susceptible strains of the following bacteria in the conditions listed below: conjunctivitis: gram-positive bacteria: staphylococcus aureus staphylococcus epidermidis streptococcus pneumoniae gram-negative bacteria: enterobacter cloacae haemophilus influenzae proteus mirabilis pseudomonas aeruginosa corneal ulcers: gram-positive bacteria: staphylococcus aureus staphylococcus epidermidis streptococcus pneumoniae gram-negative bacteria: pseudomonas aeruginosa serratia marcescens* anaerobic species: propionibacterium acnes *efficacy for this organism was studied in fewer than 10 infections
Warnings:
Warnings not for injection ofloxacin ophthalmic solution should not be injected subconjunctivally, nor should it be introduced directly into the anterior chamber of the eye. serious and occasionally fatal hypersensitivity (anaphylactic) reactions, some following the first dose, have been reported in patients receiving systemic quinolones, including ofloxacin. some reactions were accompanied by cardiovascular collapse, loss of consciousness, angioedema (including laryngeal, pharyngeal or facial edema), airway obstruction, dyspnea, urticaria, and itching. a rare occurrence of stevens-johnson syndrome, which progressed to toxic epidermal necrolysis, has been reported in a patient who was receiving topical ophthalmic ofloxacin. if an allergic reaction to ofloxacin occurs, discontinue the drug. serious acute hypersensitivity reactions may require immediate emergency treatment. oxygen and airway management, including intubation should be administered as clinically indicated.
General Precautions:
General: as with other anti-infectives, prolonged use may result in overgrowth of nonsusceptible organisms, including fungi. if superinfection 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. ofloxacin should be discontinued at the first appearance of a skin rash or any other sign of hypersensitivity reaction. the systemic administration of quinolones, including ofloxacin, has led to lesions or erosions of the cartilage in weight-bearing joints and other signs of arthropathy in immature animals of various species. ofloxacin, administered systemically at 10 mg/kg/day in young dogs (equivalent to 110 times the maximum recommended daily adult ophthalmic dose) has been associated with these types of effects.
Dosage and Administration:
Dosage and administration the recommended dosage regimen for the treatment of bacterial conjunctivitis is: days 1 and 2 instill one to two drops every two to four hours in the affected eye(s). days 3 through 7 instill one to two drops four times daily. the recommended dosage regimen for the treatment of bacterial corneal ulcer is: days 1 and 2 instill one to two drops into the affected eye every 30 minutes, while awake. awaken at approximately four and six hours after retiring and instill one to two drops. days 3 through 7 to 9 instill one to two drops hourly, while awake. days 7 to 9 through instill one to two drops, four times daily. treatment completion do not use if imprinted âprotective sealâ with yellow is not intact. symbol
Contraindications:
Contraindications ofloxacin ophthalmic solution is contraindicated in patients with a history of hypersensitivity to ofloxacin, to other quinolones, or to any of the components in this medication.
Adverse Reactions:
Adverse reactions ophthalmic use: the most frequently reported drug-related adverse reaction was transient ocular burning or discomfort. other reported reactions include stinging, redness, itching, chemical conjunctivitis/keratitis, ocular/periocular/facial edema, foreign body sensation, photophobia, blurred vision, tearing, dryness, and eye pain. rare reports of dizziness and nausea have been received.
Drug Interactions:
Drug interactions: specific drug interaction studies have not been conducted with ofloxacin ophthalmic solution. however, the systemic administration of some quinolones has been shown to elevate plasma concentrations of theophylline, interfere with the metabolism of caffeine, and enhance the effects of the oral anticoagulant warfarin and its derivatives, and has been associated with transient elevations in serum creatinine in patients receiving cyclosporine concomitantly.
Pediatric Use:
Pediatric use: safety and effectiveness in infants below the age of one year have not been established. quinolones, including ofloxacin, have been shown to cause arthropathy in immature animals after oral administration; however, topical ocular administration of ofloxacin to immature animals has not shown any arthropathy. there is no evidence that the ophthalmic dosage form of ofloxacin has any effect on weight bearing joints.
Geriatric Use:
Geriatric use: no overall differences in safety or effectiveness have been observed between elderly and younger patients.
Description:
Description ofloxacin ophthalmic solution 0.3% is a sterile ophthalmic solution. it is a fluorinated carboxyquinolone anti-infective for topical ophthalmic use. c 18 h 20 fn 3 o 4 mol. wt. 361.37 chemical name: (±)-9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7h-pyrido[1,2,3-de]-1,4 benzoxazine-6-carboxylic acid. each ml contains: active: ofloxacin 0.3% (3 mg/ml) preservative added: benzalkonium chloride (0.005%) inactives : sodium chloride and purified water. hydrochloric acid and/or sodium hydroxide may be added to adjust ph. ofloxacin ophthalmic solution is unbuffered and formulated with a ph of 6.4 (range - 6.0 to 6.8). it has an osmolality of 300 mosm/kg. ofloxacin is a fluorinated 4-quinolone which differs from other fluorinated 4-quinolones in that there is a six member (pyridobenzoxazine) ring from positions 1 to 8 of the basic ring structure. ofloxacin (structural formula)
Clinical Pharmacology:
Clinical pharmacology pharmacokinetics: serum, urine and tear concentrations of ofloxacin were measured in 30 healthy women at various time points during a ten-day course of treatment with ofloxacin ophthalmic solution. the mean serum ofloxacin concentration ranged from 0.4 ng/ml to 1.9 ng/ml. maximum ofloxacin concentration increased from 1.1 ng/ml on day one to 1.9 ng/ml on day 11 after qid dosing for 10 1/2 days. maximum serum ofloxacin concentrations after ten days of topical ophthalmic dosing were more than 1000 times lower than those reported after standard oral doses of ofloxacin. tear ofloxacin concentrations ranged from 5.7 to 31 mcg/g during the 40 minute period following the last dose on day 11. mean tear concentration measured four hours after topical ophthalmic dosing was 9.2 mcg/g. corneal tissue concentrations of 4.4 mcg/ml were observed four hours after beginning topical ocular application of two drops of ofloxacin ophthalmic solution every 30 minutes. ofloxacin was exc
Read more...reted in the urine primarily unmodified. microbiology: ofloxacin has in vitro activity against a broad range of gram-positive and gram-negative aerobic and anaerobic bacteria. ofloxacin is bactericidal at concentrations equal to or slightly greater than inhibitory concentrations. ofloxacin is thought to exert a bactericidal effect on susceptible bacterial cells by inhibiting dna gyrase, an essential bacterial enzyme which is a critical catalyst in the duplication, transcription, and repair of bacterial dna. cross-resistance has been observed between ofloxacin and other fluoroquinolones. there is generally no cross-resistance between ofloxacin and other classes of antibacterial agents such as beta-lactams or aminoglycosides. ofloxacin has been shown to be active against most strains of the following organisms both in vitro and clinically, in conjunctival and/or corneal ulcer infections as described in the indications and usage section. aerobes, gram-positive: staphylococcus aureus staphylococcus epidermidis streptococcus pneumoniae aerobes, gram-negative: enterobacter cloacae haemophilus influenzae proteus mirablis pseudomonas aeruginosa serratia marcescens* anaerobic species: propionibacterium acnes *efficacy for this organism was studied in fewer than 10 infections the safety and effectiveness of ofloxacin ophthalmic solution in treating ophthalmologic infections due to the following organisms have not been established in adequate and well-controlled clinical trials. ofloxacin ophthalmic solution has been shown to be active in vitro against most strains of these organisms but the clinical significance in ophthalmologic infections is unknown. aerobes, gram-positive: enterococcus faecalis listeria monocytogenes staphylococcus capitis staphylococcus hominus staphylococcus simulans streptococcus pyogenes aerobes, gram-negative: acinetobacter calcoaceticus var. anitratus acinetobacter calcoaceticus var. lwoffi citrobacter diversus citrobacter freundii enterobacter aerogenes enterobacter agglomerans escherichia coli haemophilus parainfluenzae klebsiella oxytoca klebsiella pneumoniae moraxella (branhamella) catarrhalis moraxella lacunata morganella morganii neisseria gonorrhoeae pseudomonas acidovorans pseudomonas fluorescens shigella sonnei other: chlamydia trachomatis clinical studies: conjunctivitis: in a randomized, double-masked, multicenter clinical trial, ofloxacin ophthalmic solution was superior to its vehicle after 2 days of treatment in patients with conjunctivitis and positive conjunctival cultures. clinical outcomes for the trial demonstrated a clinical improvement rate of 86% (54/63) for the ofloxacin treated group versus 72% (48/67) for the placebo treated group after 2 days of therapy. microbiological outcomes for the same clinical trial demonstrated an eradication rate for causative pathogens of 65% (41/63) for the ofloxacin treated group versus 25% (17/67) for the vehicle treated group after 2 days of therapy. please note that microbiologic eradication does not always correlate with clinical outcome in anti-infective trials. corneal ulcers: in a randomized, double-masked, multi-center clinical trial of 140 subjects with positive cultures, ofloxacin ophthalmic solution treated subjects had an overall clinical success rate (complete re-epithelialization and no progression of the infiltrate for two consecutive visits) of 82% (61/74) compared to 80% (53/66) for the fortified antibiotic group, consisting of 1.5% tobramycin and 10% cefazolin solutions. the median time to clinical success was 11 days for the ofloxacin treated group and 10 days for the fortified treatment group.
Carcinogenesis and Mutagenesis and Impairment of Fertility:
Carcinogenesis, mutagenesis, impairment of fertility: long term studies to determine the carcinogenic potential of ofloxacin have not been conducted. ofloxacin was not mutagenic in the ames test, in vitro and in vivo cytogenic assay, sister chromatid exchange assay (chinese hamster and human cell lines), unscheduled dna synthesis (uds) assay using human fibroblasts, the dominant lethal assay, or mouse micronucleus assay. ofloxacin was positive in the uds test using rat hepatocyte, and in the mouse lymphoma assay. in fertility studies in rats, ofloxacin did not affect male or female fertility or morphological or reproductive performance at oral dosing up to 360 mg/kg/day (equivalent to 4000 times the maximum recommended daily ophthalmic dose).
How Supplied:
How supplied ofloxacin ophthalmic solution 0.3% is supplied sterile in plastic dropper bottles in the following sizes: 5 ml ndc 63187-268-05
Information for Patients:
Information for patients: avoid contaminating the applicator tip with material from the eye, fingers or other source. systemic quinolones, including ofloxacin, have been associated with hypersensitivity reactions, even following a single dose. discontinue use immediately and contact your physician at the first sign of a rash or allergic reaction.
Package Label Principal Display Panel:
Package/label principal display panel 63187-268-05