Toggle menu
Toggle preferences menu
Toggle personal menu
Not logged in
Your IP address will be publicly visible if you make any edits.

Ciprofloxacin

Unchecked
From Pharmacopedia
Ciprofloxacin
Cipro, Cipro XR, Ciloxan (ophthalmic)

Experience

👥 No personal reports yet
No clinical reports yet

Log in to add your own experience.

Problems

No problems yet. Be the first to suggest one.

+ Add a problem

Titration strategies

No titration strategies yet. Be the first to suggest one.

+ Add a titration strategy

Effects

No effects listed yet. Be the first to suggest one.

+ Add an effect

Relevant anecdote

No anecdotes yet. Share a relevant one.

+ Add an anecdote

Relevant Literature

No literature entries yet.

Log in to submit relevant literature.

Summary
Common uses
Complicated UTI / pyelonephritis0, Bacterial prostatitis0, Bacterial gastroenteritis (selected)0, Pseudomonal coverage (selected)0, Anthrax prophylaxis and treatment0, Bacterial conjunctivitis/keratitis (topical)0
Pharmacy
Starting dose
500-750 mg PO BID; 400 mg IV q8-12h
Preparations
250, 500, 750 mg IR tablets; 500, 1000 mg ER tablets (XR); 250, 500 mg/5 mL oral suspension; 200, 400 mg IV; 0.3% ophthalmic solution and ointment; 0.2% otic
US FDA Max
~1500 mg/d (oral); 1200 mg/d (IV)
Pharmacology
Routes
Oral, IV, topical ophthalmic, otic
Onset
Hours
Duration
8-12 hours
Half-life
4 hours[1]
Bioavailability
~70% (oral; reduced by divalent cations — antacids, iron, calcium, dairy)[1]
Pregnancy
Avoid in pregnancy where alternatives exist (animal cartilage toxicity; class-wide concern); use only when benefit clearly outweighs.[citation needed]
Legal status
Rx-only in US. Carries Boxed Warnings for tendinitis/tendon rupture (especially elderly, corticosteroid co-use, post-transplant), peripheral neuropathy (sometimes irreversible), CNS effects (psychosis, seizure), and worsening of myasthenia gravis[1]
Purported mechanism
Ciprofloxacin inhibits bacterial DNA gyrase (topoisomerase II, dominant in gram-negatives) and topoisomerase IV (dominant in gram-positives), preventing supercoiling and decatenation needed for DNA replication; the result is bactericidal at clinically achievable concentrations.0 CYP1A2 inhibitor — clinically meaningful interactions with theophylline, caffeine, and tizanidine. QT prolongation, hypoglycemia (especially with sulfonylureas), and aortic aneurysm/dissection signals add to the class-wide reasons FDA has progressively restricted fluoroquinolone use to indications where alternatives have failed[1].

References

edit
  1. 1.0 1.1 1.2 1.3 FDA Prescribing Information, Cipro (ciprofloxacin), Bayer, current revision. https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019537s086,019847s060,019857s062,020780s041lbl.pdf