🇺🇸 Ciprofloxacin 750 mg in United States

12 US adverse-event reports

Marketing authorisation

FDA

  • Status: approved

Safety signals — FAERS

Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.

Most-reported reactions

  1. Dizziness — 2 reports (16.67%)
  2. Pain — 2 reports (16.67%)
  3. Abdominal Pain Upper — 1 report (8.33%)
  4. Acute Kidney Injury — 1 report (8.33%)
  5. Acute Psychosis — 1 report (8.33%)
  6. Affect Lability — 1 report (8.33%)
  7. Anal Haemorrhage — 1 report (8.33%)
  8. Anger — 1 report (8.33%)
  9. Angina Pectoris — 1 report (8.33%)
  10. Anxiety — 1 report (8.33%)

Source database →

Ciprofloxacin 750 mg in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is Ciprofloxacin 750 mg approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Ciprofloxacin 750 mg in United States?

Future University in Egypt is the originator. The local marketing authorisation holder may differ — check the official source linked above.