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IV: mg IV every 12 hours Oral: mg orally every 12 hours Duration of Therapy: 7 to 14 days Use: In combination with metronidazole, for treatment of complicated intraabdominal infections due to Escherichia coli, Pseudomonas aeruginosa, Proteus mirabilis, Klebsiella pneumoniae, or Bacteroides fragilis. Use: For treatment of nosocomial pneumonia due to Haemophilus influenzae or K pneumoniae. Use: For treatment of acute sinusitis due to H influenzae, S pneumoniae, or M catarrhalis. Fecal samples should be obtained for diagnostic testing before starting therapy; therapy should be adjusted based on those results. Cipro R XR: mg orally every 24 hours for 7 to 14 days Use: For the treatment of acute uncomplicated pyelonephritis due to E coli. This drug should be discontinued immediately and use of fluoroquinolones including this drug should be avoided in patients with any of these serious side effects. This drug should be avoided in patients with known history of myasthenia gravis. Administration advice Infuse IV doses over at least 60 minutes; slow infusion of dilute solution into larger vein will minimize patient discomfort and reduce risk of venous irritation.

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Drugs» Infectious Diseases. 1000 mg of ciprofloxacin infections including UTIs, acute uncomplicated pyelonephritis. For uncomplicated UTIs: reserve for those who have no alternative treatment options. Coincide dose for end of dialysis. Serious adverse reactions including tendinitis and tendon rupture, peripheral neuropathy, CNS effects.

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Ciprofloxacin was used as an antituberculous drug in adult patients who could not tolerate standard regimens or had to be treated with alternative combinations for resistance problems. During October to December, patients received ciprofloxacin in two daily mg doses administered under supervision at 8. Until July, patients with smear-positive pulmonary tuberculosis were included in this open study. Comparative analysis was carried out for a selected group of patients who had remained smear and culture positive for more than 27 days after start of treatment. Fifty-four patients who had received ciprofloxacin twice daily and 35 patients on the once daily regimen were evaluable.

Limitations-of-use: Reserve fluoroquinolones for patients who do not have other available treatment options for acute sinusitis. Limitations-of-use: Reserve fluoroquinolones for patients who do not have other available treatment options for acute bacterial exacerbation of chronic bronchitis. Acute uncomplicated: Immediate-release, mg PO q12hr for 3 days; extended-release, mg PO q24hr for 3 days. Limitations-of-use: Reserve fluoroquinolones for patients who do not have other available treatment options for uncomplicated urinary tract infections. Dry powder for inhalation: Orphan designation for patients with NCFB who suffer from frequent severe acute pulmonary bacterial exacerbations which lead to further inflammation, airway, and lung parenchyma damage.

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Adolescents and Adults age 12 years and older Cellulitis - - mg twice a day or mg once daily for 10 days PI Sinusitis - - mg twice a day for 10 days PI Strep throat - mg once daily for 10 days PI. Suspension and tablet are not bioequivalent on a mg-to-mg basis. Adults and Adolescents Age 13 years and older Pneumonia, community-acquired - mg twice a day for 10 days PI Sinusitis - mg twice a day or mg once daily for 10 days IDSA Skin infections - mg twice a day for 10 days PI Strep throat - mg twice a day for 5 - 10 days or mg once daily for 10 days PI Urinary tract infection - mg twice a day for 3 - 7 days IDSA. Do not take within 2 hours of each other. Adults and Adolescents Age 12 years and older Pneumonia, community-acquired - mg twice a day for 14 days PI Skin infections - mg twice a day for 10 days PI Strep throat - mg twice a day for 10 days PI.

WikiDoc is not a professional health care provider, nor is it a suitable replacement for a licensed healthcare provider. WikiDoc does not promote the administration of any medication or device that is not consistent with its labeling. Common adverse reactions include rash, diarrhea, headache, cardiorespiratory arrest, photosensitivity, agranulocytosis, hepatic necrosis, tendinitis, raised intracranial pressure, retinal detachment, depression, and acute renal failure. There is no FDA guidance on the use of Ciprofloxacin oral with respect to specific gender populations. There is no FDA guidance on the use of Ciprofloxacin oral with respect to specific racial populations.

Cipro may be used alone or with other medications. These are not all the possible side effects of Cipro. Cipro tablets are coated, bilayer tablets consisting 1000 mg of ciprofloxacin an immediate-release layer and an erosion -matrix type controlled-release layer. The tablets contain a combination of two types of ciprofloxacin drug substance, ciprofloxacin hydrochloride and ciprofloxacin betaine base. Ciprofloxacin hydrochloride is 1-cyclopropylfluoro-1,4dihydrooxo 1-piperazinyl quinolinecarboxylic acid hydrochloride.

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