🇺🇸 Cavir in United States

10 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. Abdominal Pain — 1 report (10%)
  2. Ascites — 1 report (10%)
  3. Constipation — 1 report (10%)
  4. Cough — 1 report (10%)
  5. Diarrhoea — 1 report (10%)
  6. Hypertension — 1 report (10%)
  7. Hypoalbuminaemia — 1 report (10%)
  8. Neutropenia — 1 report (10%)
  9. Paraesthesia — 1 report (10%)
  10. Pharyngitis — 1 report (10%)

Source database →

Cavir in other countries

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

Other Other approved in United States

Frequently asked questions

Is Cavir approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Cavir in United States?

Hanmi Pharmaceutical Company Limited is the originator. The local marketing authorisation holder may differ — check the official source linked above.