Ciprofloxacin Otic

Ciprofloxacin Otic Solution is for otic use only. It should not be used for injection, for inhalation or for topical ophthalmic use.

Ciprofloxacin Otic Solution should be discontinued at the first appearance of a skin rash or any other sign of hypersensitivity.

As with other anti-infectives, use of Ciprofloxacin Otic Solution may result in overgrowth of nonsusceptible organisms, including yeast and fungi. If super-infection occurs, discontinue use and institute alternative therapy.

If the infection is not improved after one week of therapy, cultures may help guide further treatment.

Ciprofloxacin is excreted in human milk with systemic use. It is not known whether ciprofloxacin is excreted in human milk following otic use. Because of the potential for serious adverse reactions in nursing infants, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

The safety and effectiveness of Ciprofloxacin Otic Solution in infants below one year of age have not been established. The efficacy of Ciprofloxacin Otic Solution in treating otitis externa in pediatric patients one year or older has been demonstrated in controlled clinical trials (see Section 14 Clinical Studies).

There is no evidence that the otic 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.

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

Ciprofloxacin is a fluoroquinolone antimicrobial (see 12.4 Clinical Pharmacology, Microbiology).

The plasma concentrations of ciprofloxacin were not measured following administration of 0.25 mL Ciprofloxacin Otic Solution (total dose: 0.5 mg ciprofloxacin). However, the maximum plasma concentration of ciprofloxacin is anticipated to be less than 5 ng/mL.

The bactericidal action of ciprofloxacin results from interference with the enzyme DNA gyrase, which is needed for the synthesis of bacterial DNA.

Bacterial resistance to quinolones can develop through chromosomally- or plasmid-mediated mechanisms.

The mechanism of action of fluoroquinolones, including ciprofloxacin, is different from that of macrolides. Therefore, ciprofloxacin may be active against pathogens that are resistant to these antibiotics, and these antibiotics may be active against pathogens that are resistant to ciprofloxacin. In vitrostudies demonstrated cross-resistance between ciprofloxacin and some fluoroquinolones.

Ciprofloxacin has been shown to be active against most isolates of the following bacteria, both in vitroand in clinical infections of acute otitis externa as described in Section 1 Indications and Usage.

• Staphylococcus aureus
• Pseudomonas aeruginosa.

Long-term carcinogenicity studies in mice and rats have been completed for ciprofloxacin. After daily oral doses of 750 mg/kg (mice) and 250 mg/kg (rats) were administered for up to 2 years, there was no evidence that ciprofloxacin had any carcinogenic or tumorigenic effects in these species. No long-term studies of Ciprofloxacin Otic Solution have been performed to evaluate carcinogenic potential.

Eight in vitromutagenicity tests have been conducted with ciprofloxacin, and the test results are listed below:

• Salmonella/Microsome Test (Negative)
• Escherichia coliDNA Repair Assay (Negative)
• Mouse Lymphoma Cell Forward Mutation Assay (Positive)
• Chinese Hamster V79 Cell HGPRT Test (Negative)
• Syrian Hamster Embryo Cell Transformation Assay (Negative)
• Saccharomyces cerevisiaePoint Mutation Assay (Negative)
• Saccharomyces cerevisiaeMitotic Crossover and Gene Conversion Assay (Negative)
• Rat Hepatocyte DNA Repair Assay (Positive).

Two of the 8 in vitrotests were positive, but results of the following 3 in vivotest systems gave negative results:

• Rat Hepatocyte DNA Repair Assay
• Micronucleus Test (Mice)
• Dominant Lethal Test (Mice).

Fertility studies performed in rats at oral doses of ciprofloxacin up to 100 mg/kg/day revealed no evidence of impairment. This would be over 100 times the maximum recommended clinical dose of ototopical ciprofloxacin based upon body surface area, assuming total absorption of ciprofloxacin from the ear of a patient treated with Ciprofloxacin Otic Solution twice per day.

Store at 15ºC to 25ºC (59ºF to 77ºF). Discard used containers. Store unused containers in pouch to protect from light.

Patients should be advised that Ciprofloxacin Otic Solution is for otic use only. It is not for ophthalmic or inhalation use. It is not for injection.

Ciprofloxacin Otic Solution should be given 2 times each day (about 12 hours apart) in each infected ear.

Ciprofloxacin Otic Solution should be used for as long as it is prescribed, even if the symptoms improve. The patient should be advised to follow these directions while on Ciprofloxacin Otic Solution:

• Wash their hands before use.
  

  Figure

• Warm the container in their hands for at least one minute prior to use to minimize dizziness that may result from the instillation of a cold solution into the ear canal. Twist off and discard top of container.
  

  Figure

• Lie with the affected ear upward and then instill the contents of one container into the ear. Maintain this position for at least one minute to facilitate penetration of the drops into the ear.
  

  Figure

• Repeat, if necessary, for the opposite ear.
• Discard used container.
• Store unused containers in pouch to protect from light.

Patients should be advised to immediately discontinue Ciprofloxacin Otic Solution at the first appearance of a skin rash or any other sign of hypersensitivity [see Section 5.1 Warnings and Precautions].