🇺🇸 Anavip in United States

243 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. Urticaria — 61 reports (25.1%)
  2. Pruritus — 48 reports (19.75%)
  3. Rash — 29 reports (11.93%)
  4. Anaphylactic Reaction — 22 reports (9.05%)
  5. Dyspnoea — 18 reports (7.41%)
  6. Erythema — 16 reports (6.58%)
  7. Off Label Use — 14 reports (5.76%)
  8. Hypersensitivity — 13 reports (5.35%)
  9. Nausea — 11 reports (4.53%)
  10. Underdose — 11 reports (4.53%)

Source database →

Other Other approved in United States

Frequently asked questions

Is Anavip approved in United States?

Yes. FDA has authorised it.

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

Instituto Bioclon S.A. de C.V. is the originator. The local marketing authorisation holder may differ — check the official source linked above.