ciprofloxacin
fluoroquinolone antibiotic· Brands: Cipro, Ciproxin, Cifran, CiprofarIVPOTOP
Complicated urinary tract infection
Typically 7-14 days. Adjust dose in renal impairment.
- adult · PO: 500 mg twice daily · Typically 7-14 days. Adjust dose in renal impairment.
Acute pyelonephritis
Duration 7-14 days. For severe infection, consider initial IV therapy.
- adult · PO: 500–750 mg twice daily · Duration 7-14 days. For severe infection, consider initial IV therapy.
Chronic bacterial prostatitis
Duration 28 days. Consider culture and susceptibility.
- adult · PO: 500 mg twice daily · Duration 28 days. Consider culture and susceptibility.
Inhalational anthrax (post-exposure)
Give soon after suspected exposure. Duration 60 days for post-exposure prophylaxis.
- adult · PO: 500 mg twice daily · Give soon after suspected exposure. Duration 60 days for post-exposure prophylaxis.
Skin and soft tissue infections
Duration depends on severity; generally 7-14 days.
- adult · PO: 500–750 mg twice daily · Duration depends on severity; generally 7-14 days.
Severe systemic infections when oral therapy inappropriate
For severe or complicated infections. Switch to oral therapy as soon as clinically appropriate.
- adult · IV: 200–400 mg every 12 hours · For severe or complicated infections. Switch to oral therapy as soon as clinically appropriate.
- Hypersensitivity to ciprofloxacin or other fluoroquinolones · Includes rash, angio-oedema, anaphylaxis.
- Concomitant use with tizanidine · Risk of severe hypotension and sedation due to CYP1A2 inhibition.
- History of tendon disorders with fluoroquinolones · Risk of recurrent tendinopathy or rupture.
- Pregnancy and breastfeeding · Only use if potential benefit outweighs risk; consider alternatives.
- Children under 18 years · Risk of arthropathy; use only for specific infections with no alternative.
- Use with caution in epilepsy or history of seizures.
- Use with caution in QT prolongation, electrolyte disturbances, or with other QT-prolonging drugs.
- Discontinue treatment if tendon pain or signs of peripheral neuropathy occur.
- Avoid exposure to sunlight and UV lamps; use sun protection.
- Separate administration of antacids, iron, zinc, or calcium supplements by at least 2 hours.
- Adjust dose in renal impairment.
- Nausea
- Diarrhoea
- Headache
- Tendonitis or tendon ruptureserious
- QT interval prolongationserious
- Peripheral neuropathyserious
- Seizuresserious
- Photosensitivity
- warfarinmajorPrescribers should avoid concurrent use if possible, especially in patients with other bleeding risk factors. If co-prescription is necessary, closely monitor the INR at baseline, after 2 to 3 days, and then regularly throughout treatment. Adjust the warfarin dose as needed and warn the patient to seek medical attention if signs of bleeding occur.
- theophyllinemajorAvoid concurrent use if possible, as alternative antibiotics with minimal CYP1A2 inhibition (e.g., levofloxacin) may be considered. If co-prescription is necessary, reduce the theophylline dose by up to 50% and closely monitor serum theophylline concentrations and clinical signs of toxicity. Repeat theophylline levels should be measured after initiating or adjusting ciprofloxacin therapy, and further dose adjustments made as required.
- amiodaronemajorConsider alternative antibiotics with less QT prolonging activity, such as doxycycline, if clinically appropriate.
- eGFR 0–29: Reduce dose by 50% or extend dosing interval to 24 hours (e.g., 250-500 mg PO once daily; IV: 200-400 mg once daily).
- Renal function (serum creatinine, BUN) · Baseline and at least twice weekly during treatment in elderly or dehydrated patients
- Liver function tests (ALT, AST) · Baseline and if symptoms of hepatotoxicity occur
- Tendon pain or inflammation · Assess at each visit; discontinue if tendonitis or tendon rupture is suspected
- Blood glucose · Monitor in diabetic patients, as fluoroquinolones can cause dysglycaemia
- ECG (QT interval) · In patients with risk factors for QT prolongation (e.g., electrolyte disturbances, concurrent QT-prolonging drugs)
- Pregnancy: Ciprofloxacin is not recommended during pregnancy, especially in the first trimester, due to a potential risk of fetal cartilage damage. Use only if the potential benefit outweighs the risk and no alternative is suitable.
- Toxicity: Tendonitis or tendon rupture · Discontinue at first sign of tendon pain or inflammation; rest the affected limb and avoid exercise.
- Toxicity: QT interval prolongation and ventricular arrhythmias · Discontinue if QTc prolongation occurs; correct any electrolyte disturbances and monitor ECG.
- Toxicity: CNS effects including seizures and confusion · Discontinue; manage seizures if they occur; consider anticonvulsant therapy for severe cases.
- Toxicity: Crystalluria and renal dysfunction · Maintain adequate hydration (especially in elderly or those with reduced fluid intake); monitor renal function.
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BNF; local formulary