🇺🇸 Cefepime 2000 mg in United States

11 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. Febrile Neutropenia — 2 reports (18.18%)
  2. Acute Kidney Injury — 1 report (9.09%)
  3. Acute Respiratory Failure — 1 report (9.09%)
  4. Bacillus Test Positive — 1 report (9.09%)
  5. Covid-19 Pneumonia — 1 report (9.09%)
  6. Diarrhoea — 1 report (9.09%)
  7. Fall — 1 report (9.09%)
  8. Hypotension — 1 report (9.09%)
  9. Hypovolaemia — 1 report (9.09%)
  10. Hypoxia — 1 report (9.09%)

Source database →

Cefepime 2000 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 Cefepime 2000 mg approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Cefepime 2000 mg in United States?

Wockhardt is the originator. The local marketing authorisation holder may differ — check the official source linked above.