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the doorstep [2:<1 year of age. 1 Ciprofloxacin-dexamethasone otic suspension: Safety and efficacy not established in children> <6 months of age, but there are no known safety concerns or differences in disease process to preclude use in children> <6 months of age. 125 Ciprofloxacin-hydrocortisone otic suspension: Safety and efficacy not established in children> <2 years of age, but there are no known safety concerns or differences in disease process to preclude use in children 1 year of age. 120 Common Adverse Effects Ophthalmic: local burning or discomfort, lid margin crusting, crystals/scales, foreign body sensation, itching, conjunctival hyperemia, bad taste, keratopathy. 1 119 Otic: otic discomfort/pain/pruritus. 120 125 Interactions for Ciloxan No formal drug interaction studies to date. 1 119 125 Since systemic absorption may occur following ophthalmic or otic 1 119 125 administration, consider possible drug interactions such as those reported with systemic administration. 1 119 125 Ciloxan Pharmacokinetics Absorption Bioavailability Ophthalmic ointment: Extent of systemic absorption not evaluated, but mean maximal plasma ciprofloxacin concentrations expected to be> <2.5 ng/mL, based on studies using 0.3% ophthalmic solution. 119 Ophthalmic solution: Mean plasma ciprofloxacin concentrations generally averaged> <2.5 ng/mL after topical application to each eye (1 drop of 0.3% ophthalmic solution every 2 hours while awake for 2 days, then every 4 hours while awake for 5 days). 1 Ciprofloxacin-dexamethasone otic suspension: Following a single bilateral 4-drop otic dose in pediatric patients after tympanostomy tube insertion, measurable plasma ciprofloxacin or dexamethasone concentrations were observed after 6 hours in 2 or 5 of 9 patients, respectively. 125 Peak plasma ciprofloxacin and dexamethasone concentrations were attained within 15 minutes to 2 hours. 125 Ciprofloxacin-hydrocortisone otic suspension: Systemic exposure to ciprofloxacin expected to be below assay quantitation limits (0.05 mg/mL) and maximum plasma hydrocortisone concentration is predicted to be within range of endogenous hydrocortisone. 120 Distribution Extent Distribution into human ocular tissues and fluids following topical ophthalmic or systemic administration not fully characterized to date. 8 17 Distributed into milk after systemic administration; it is not known whether distributed into milk after topical application to the eye or ear. 1 119 120 125 Stability Storage Ophthalmic Ointment 2 25 C. 119 Solution 2 25 C. 1 Protect from light. 1 108 Otic Suspension Ciprofloxacin-dexamethasone otic suspension: 15 30 C. 125 Avoid freezing; protect from light. 125 Ciprofloxacin-hydrocortisone otic suspension:> <25 C. 120 Avoid freezing; protect from light. 120 Actions and Spectrum Inhibits DNA synthesis via inhibition of type II DNA topoisomerases (DNA gyrase, topoisomerase IV). 1 3 7 31 36 43 44 50 51 52 53 99 Usually bactericidal. 1 3 6 37 40 41 42 43 44 45 47 Active in vitro against most gram-negative aerobic bacteria and many gram-positive aerobic bacteria, 1 3 5 8 30 31 32 40 42 46 54 including penicillinase-producing, nonpenicillinase-producing, and oxacillin-resistant staphylococci; 1 3 5 8 30 31 40 42 46 59 60 generally less active against gram-positive than gram-negative bacteria 30 31 42 46 67 68 69 and less active in vitro on a weight basis against streptococci than against staphylococci. 3 5 6 8 40 42 64 65 66 67 68 Most strains of Ps. cepacia , some strains of Ps. maltophilia , and most anaerobic bacteria, including Bacteroides fragilis and Clostridium difficile , are resistant. 1 3 Inactive against fungi and viruses. 1 3 5 6 8 Advice to Patients Importance of discontinuing drug and informing clinician at first sign of rash or other sign of hypersensitivity. 1 99 116 119 120 125 Importance of learning and adhering to proper administration techniques to avoid contamination of the product. 1 116 119 120 125 Importance of not wearing contact lenses in presence of signs and symptoms of ophthalmic bacterial infections. 119 Importance of informing clinicians of existing or contemplated therapy, including prescription and OTC drugs. 1 119 120 125 Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed. 1 119 120 125 Importance of informing patients of other important precautionary information. (See Cautions.) 1 119 120 125 Preparations Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details. Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations. Ciprofloxacin Hydrochloride Routes Dosage Forms Strengths Brand Names Manufacturer Ophthalmic Ointment 0.3% (of ciprofloxacin) Ciloxan Alcon Solution 0.3% (of ciprofloxacin) Ciloxan (with benzalkonium chloride) Alcon Ciprofloxacin Ophthalmic Solution (with benzalkonium chloride) Bausch & Lomb, Hi-Tech, Novex Ciprofloxacin Hydrochloride Combinations Routes Dosage Forms Strengths Brand Names Manufacturer Otic Suspension 0.2% (of ciprofloxacin) with Hydrocortisone 1% Cipro HC Otic Drops (with benzyl alcohol 0.9%) Alcon 0.3% (of ciprofloxacin) with Dexamethasone 0.1% Ciprodex (with benzalkonium chloride) Alcon AHFS DI Essentials. Copyright 2017, Selected Revisions July 1, 2006. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814. References 1. Alcon Laboratories. Ciloxan (ciprofloxacin hydrochloride) ophthalmic solution prescribing information. Fort Worth, TX; 1999 Dec. 2. Alcon Laboratories. Product information form for American hospital formulary service: Ciloxan (ciprofloxacin HCl) 0.3% as base sterile ophthalmic solution. Fort Worth, TX: 1991 Mar. 3. Alcon Laboratories. Ciloxan product monograph. Ciloxan (ciprofloxacin HCl) 0.3% as base sterile ophthalmic solution. Fort Worth, TX: 1991 Apr. 4. Anon. Ophthalmic ciprofloxacin. Med Lett Drugs Ther . 1991; 33:52-3. [PubMed 2030657] 5. Campoli-Richards DM, Monk JP, Price A et al. Ciprofloxacin: a review of its antibacterial activity, pharmacokinetic properties and therapeutic use. Drugs . 1988; 35:373-447. [PubMed 3292209] 6. Neu HC. Microbiologic aspects of fluoroquinolones. 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Intravitreal penetration of oral ciprofloxacin in humans. Ophthalmology . 1992; 99:483-6. [PubMed 1584563] 19. Gardner DK, Gabbe SG, Harter C. Simultaneous concentrations of ciprofloxacin in breast milk and in serum in mother and breast-fed infant. Clin Pharm . 1992; 11: 352-4. [PubMed 1563233] 20. Cover DL, Mueller BA. Ciprofloxacin penetration into human breast milk: a case report. DICP . 1990; 24:703-4. [PubMed 2375140] 21. Giamarellou H, Kanellas D, Kavouklis E et al. Comparative pharmacokinetics of ciprofloxacin, ofloxacin and pefloxacin in human aqueous humour. Eur J Clin Microbiol Infect Dis . 1993; 12:293-7. [PubMed 8513819] 22. Limberg MB. A review of bacterial keratitis and bacterial conjunctivitis. Am J Ophthalmol . 1991; 112:2-9S. 23. McDonnell PJ, Green WR. Conjunctivitis. In: Mandell GL, Douglas RG Jr, Bennett JE, eds. Principles and practices of infectious diseases. 3rd ed. New York: Churchill Livingstone; 1990:975-82. 24. Steinert RF. Current therapy for bacterial keratitis and bacterial conjunctivitis. Am J Ophthalmol . 1991; 112:10-4S. 25. Leibowitz HM. Clinical evaluation of ciprofloxacin 0.3% ophthalmic solution for treatment of bacterial keratitis. Am J Ophthalmol . 1991; 112:34-47S. [PubMed 1882919] 26. Cokingtin CD, Hyndiuk RA. Insights from experimental data on ciprofloxacin in the treatment of bacterial keratitis and ocular infections. Am J Ophthalmol . 1991; 112:25-8S. 27. Insler MS, Fish LA, Silbernagel J et al. Successful treatment of methicillin-resistant Staphylococcus aureus keratitis with topical ciprofloxacin. Ophthalmology . 1991; 98:1690-2. [PubMed 1800931] 28. Sossi N, Feldman RM, Feldman ST et al. Mycobacterium gordonae keratitis after penetrating keratoplasty. Arch Ophthalmol . 1991; 109:1064-5. [PubMed 1867541] 29. Hwang DG, Biswell R. Ciprofloxacin therapy of Mycobacterium chelonae keratitis. Am J Ophthalmol . 1993; 115:114-5. [PubMed 8420364] 30. Nix DE, Devito JM. 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The mode of action of 4-quinolones and possible mechanisms of resistance. J Antimicrob Chemother . 1986; 18(Suppl D):21-9. [PubMed 3542946] 44. Hooper DC, Wolfson JS, Ng EY et al. Mechanisms of action of and resistance to ciprofloxacin. Am J Med . 1987; 82(Suppl 4A):12-20. [PubMed 3034057] 45. Reeves DS, Bywater MJ, Holt HA et al. In vitro studies with ciprofloxacin, a new 4-quinolone compound. J Antimicrob Chemother . 1984; 13:333-6. [PubMed 6233250] 46. Terp DK, Rybak MJ. Ciprofloxacin. Drug Intell Clin Pharm . 1987; 21:568-74. [PubMed 3301247] 47. Standiford HC, Drusano GL, Forrest A et al. Bactericidal activity of ciprofloxacin compared with that of cefotaxime in normal volunteers. Antimicrob Agents Chemother . 1987; 31:1177-82. [PubMed 3631942] 48. Thadepalli H, Bansal MB, Rao B et al. Ciprofloxacin: in vitro, experimental, and clinical evaluation. Rev Infect Dis . 1988; 10:505-15. [PubMed 3393781] 49. Diver JM, Wise R. Morphological and biochemical changes in Escherichia coli after exposure to ciprofloxacin. J Antimicrob Chemother . 1986; 18(Suppl D):31-41. [PubMed 3542947] 50. Domagala JM, Hanna LD, Heifetz CL et al. New structure-activity relationships of the quinolone antibacterials using the target enzyme: the development and application of a DNA gyrase assay. J Med Chem . 1986; 29:394-404. [PubMed 3005575] 51. Zweerink MM, Edison A. Inhibition of Micrococcus luteus DNA gyrase by norfloxacin and 10 other quinolone carboxylic acids. Antimicrob Agents Chemother . 1986; 29:598-601. [PubMed 3010848] 52. Hussy P, Maass G, Tummler B et al. Effect of 4-quinolones and novobiocin on calf thymus DNA polymerase α-primase complex, topoisomerases I and II, and growth of mammalian lymphoblasts. Antimicrob Agents Chemother . 1986; 29:1073-8. [PubMed 3015015] 53. Bearden DT, Danziger LH. Mechanism of Action of and resistance to quinolones. Pharmacotherapy . 2001; 21:224S-32S [PubMed 11642689] 54. Sanders CC. Ciprofloxacin: in vitro activity, mechanism of action, and resistance. Rev Infect Dis . 1988; 10:516-27. [PubMed 3293157] 59. Smith SM, Eng RH, Berman E. The effect of ciprofloxacin on methicillin-resistant Staphylococcus aureus . J Antimicrob Chemother . 1986; 17:287-95. [PubMed 2939049] 60. Smith SM, Eng RH. Activity of ciprofloxacin against methicillin-resistant Staphylococcus aureus . Antimicrob Agents Chemother . 1985; 688-91. (IDIS 200502) 61. King A, Shannon K, Phillips I. The in-vitro activity of ciprofloxacin compared with that of norfloxacin and nalidixic acid. J Antimicrob Chemother . 1984; 13:325-31. [PubMed 6233249] 62. Barry AL, Jones RN. In vitro activity of ciprofloxacin against gram-positive cocci. Am J Med . 1987; 82(Suppl 4A):27-32. [PubMed 3578323] 63. Chau PY, Leung YK, Ng WW. Comparative in vitro antibacterial activity of ofloxacin and ciprofloxacin against some selected gram-positive and gram-negative isolates. Infection . 1986; 14(Suppl 4):S237-9. [PubMed 3469153] 64. Mandell W, Neu HC. In vitro activity of CI-934, a new quinolone, compared with that of other quinolones and other antimicrobial agents. Antimicrob Agents Chemother . 1986; 29:852-7. [PubMed 3729343] 65. Chin NX, Brittain DC, Neu HC. In vitro activity of Ro 23-6240, a new fluorinated 4-quinolone. Antimicrob Agents Chemother . 1986; 29:675-80. [PubMed 3085584] 66. Fass RJ. In vitro activity of ciprofloxacin (Bay o 9867). Antimicrob Agents Chemother . 1983; 24:568-74. [PubMed 6228192] 67. Chin NX, Neu HC. Ciprofloxacin, a quinolone carboxylic acid compound active against aerobic and anaerobic bacteria. Antimicrob Agents Chemother . 1984; 25:319-26. [PubMed 6232895] 68. King A, Phillips I. The comparative in-vitro activity of eight newer quinolones and nalidixic acid. J Antimicrob Chemother . 1986; 18(Suppl D):1-20. [PubMed 3468100] 69. Barry AL, Jones RN, Thornsberry C et al. Antibacterial activities of ciprofloxacin, norfloxacin, oxolinic acid, cinoxacin, and nalidixic acid. Antimicrob Agents Chemother . 1984; 25:633-7. [PubMed 6233935] 70. Young LS, Berlin OG, Inderlied CB. Activity of ciprofloxacin and other fluorinated quinolones against mycobacteria. Am J Med . 1987; 82(Suppl 4A):23-6. [PubMed 3107379] 71. Gay JD, DeYoung DR, Roberts GD. In vitro activities of norfloxacin and ciprofloxacin against Mycobacterium tuberculosis , M. avium complex, M. chelonei , M. fortuitum , and M. kansasii . Antimicrob Agents Chemother . 1984; 26:94-6. [PubMed 6236748] 72. Fenlon CH, Cynamon MH. Comparative in vitro activities of ciprofloxacin and other 4-quinolones against Mycobacterium tuberculosis and Mycobacterium intracellulare . Antimicrob Agents Chemother . 1986; 29:386-8. [PubMed 2940969] 73. Aznar J, Caballero MC, Loxano MC et al. Activities of new quinoline derivatives against genital pathogens. Antimicrob Agents Chemother . 1985; 27:76-8. [PubMed 3920959] 74. Ridgway GL, Mumtaz G, Gabriel FG et al. The activity of ciprofloxacin and other 4-quinolones against Chlamydia trachomatis and mycoplasmas in vitro. Eur J Clin Microbiol . 1984; 3:344-6. [PubMed 6237903] 75. Heppleston C, Richmond S, Bailey J. Antichlamydial activity of quinolone carboxylic acids. J Antimicrob Chemother . 1985; 15:645-7. [PubMed 3159713] 76. Sanders CC, Sanders WE, Goering RV et al. Selection of multiple antibiotic resistance by quinolones, β-lactams, and aminoglycosides with special reference to cross-resistance between unrelated drug classes. Antimicrob Agents Chemother . 1984; 26:797-801. [PubMed 6098219] 77. Barry AL, Jones RN. Cross-resistance among cinoxacin, ciprofloxacin, DJ-6783, enoxacin, nalidixic acid, norfloxacin, and oxolinic acid after in vitro selection of resistant populations. Antimicrob Agents Chemother . 1984; 25:775-7. [PubMed 6234858] 78. Kaatz GW, Seo SM. Mechanism of ciprofloxacin resistance in Pseudomonas aeruginosa . 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An overview of the pharmacology of intravenously administered ciprofloxacin. Am J Med . 1987; 82(Suppl 4A):339-45. [PubMed 3578325] 99. Bayer. Cipro I.V. (ciprofloxacin) for intravenous infusion prescribing information. West Haven, CT; 2002 Jun. 100. Christ W, Lehnert T, Ulbrich B. Specific toxicologic aspects of the quinolones. Rev Infect Dis . 1988; 10(Suppl 1):S141-6. [PubMed 3279489] 101. Snyder ME, Katz HR. Ciprofloxacin-resistant bacterial keratitis. Am J Ophthalmol . 1992; 114:336-8. [PubMed 1524125] 102. Eiferman RA, Forgey DR, Snyder J. The successful treatment of bacterial corneal ulcers with ciprofloxacin. Invest Ophthalmol Vis Sci . 1991; (Suppl 32):1171. 103. Abrams DA, Sarfarazi FA, Parks DJ et al. Topical ciprofloxacin versus conventional antibiotic therapy in the treatment of ulcerative keratitis. Invest Ophthalmol Vis Sci . 1991; (Suppl 32):1171. 104. Leibowitz HM. Antibacterial effectiveness of ciprofloxacin 0.3% ophthalmic solution in the treatment of bacterial conjunctivitis. Am J Ophthalmol . 1991; 112:29-33S. 105. Stevens SX, Fouraker BD, Jensen HG. Intraocular safety of ciprofloxacin. Arch Ophthalmol . 1991; 109:1737-43. [PubMed 1841587] 107. Cutarelli PE, Lass JH, Lazarus HM et al. Topical fluoroquinolones: antimicrobial activity and in vitro corneal epithelial toxicity. Curr Eye Res . 1991; 10:557-63. [PubMed 1893771] 108. The United States pharmacopeia, 22nd rev, and The national formulary, 17th ed. Rockville, MD: The United States Pharmacopeial Convention, Inc; 1990(Suppl 5):2596-7, (Suppl 7):3031. 110. Hobden JA, Reidy JJ, O Callaghan RJ et al. Quinolones in collagen shields to treat aminoglycoside-resistant pseudomonal keratitis. Invest Ophthalmol Vis Sci . 1990; 31: 2241-3. 111. Yolton DP. New antibacterial drugs for topical ophthalmic use. Optom Clin . 1992; 2:59-72. [PubMed 1286241] 112. Parks DJ, Abrams DA, Sarfarazi FA et al. Comparison of topical ciprofloxacin to conventional antibiotic therapy in the treatment of ulcerative keratitis. Am J Ophthalmol . 1993; 115:471-7. [PubMed 8470719] 114. Lesar TS, Fiscella RG. Antimicrobial drug delivery to the eye. Drug Intell Clin Pharm . 1985; 19:642-54. [PubMed 3899562] 115. Alcon Laboratories, Fort Worth, TX: Personal communication. 116. Reviewers comments (personal observations). 117. Wilhelmus KR, Hyndiuk RA, Caldwell DR et al. 0.3% ciprofloxacin ophthalmic ointment in the treatment of bacterial keratitis. Arch Ophthalmol . 1993; 111:1210-8. [PubMed 8363464] 118. O Brien TP, Maguire MG, Fink NE et al et al. Efficacy of ofloxacin vs cefazolin and tobramycin in the therapy for bacterial keratitis: report from the Bacterial Keratitis Study Research Group. Arch Ophthalmol . 1995; 113:1257-65. [PubMed 7575256] 119. Alcon Laboratories. Ciloxan (ciprofloxacin hydrochloride) ophthalmic ointment prescribing information. Fort Worth, TX; 2000 Sep. 120. Alcon Laboratories. Cipro HC Otic (ciprofloxacin hydrochloride and hydrocortisone) otic suspension prescribing information; undated. From Alcon website (.) Accessed 2006 Apr 3. 121. Hu FR, Luh KT. Topical ciprofloxacin for treating nontuberculous mycobacterial keratitis. Ophthalmology . 1998; 105:269-72. [PubMed 9479286] 122. Alcon Laboratories, Fort Worth, TX: Personal communication. 123. Johnson MP, Ramphal R. Malignant external otitis: report on therapy with ceftazidime and review of therapy and prognosis. Clin Infect Dis . 1990; 12:173-80. 124. Hern JD, Ghufoor K, Jayaraj SM et al. ENT manifestations of Pseudomonas aeruginosa infection in HIV and AIDS. Int J Clin Pract . 1998; 52:141-4. [PubMed 9684426] 125. Alcon Laboratories. Ciprodex (ciprofloxacin hydrochloride and dexamethasone) otic suspension prescribing information. Fort Worth, TX; 2003 Jul 17. Print this page> ]} FEATURED: CAR-T Cell Therapy Overview Mechanism of Action KTE-C19 Studies KTE-C19 Cancer Targets Adverse Events Manufacturing Recently Approved Lonhala Magnair Lonhala Magnair (glycopyrrolate) is a long-acting muscarinic antagonist (LAMA) bronchodilator for... Ozempic Ozempic (semaglutide) is a glucagon-like peptide-1 (GLP-1) analog administered once-weekly for the... Ogivri Ogivri (trastuzumab-dkst) is a HER2 / neu receptor antagonist biosimilar to Herceptin indicated for... Sublocade Sublocade (buprenorphine) is a once-monthly injectable partial opioid agonist formulation for the... More} } most excellent


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