🇺🇸 Neurodex in United States

13 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. Dyspnoea — 2 reports (15.38%)
  2. Febrile Neutropenia — 2 reports (15.38%)
  3. Sepsis — 2 reports (15.38%)
  4. Blood Beryllium Decreased — 1 report (7.69%)
  5. Blood Bicarbonate Decreased — 1 report (7.69%)
  6. Blood Glucose Increased — 1 report (7.69%)
  7. Blood Ph Decreased — 1 report (7.69%)
  8. Chest X-Ray Abnormal — 1 report (7.69%)
  9. Decreased Appetite — 1 report (7.69%)
  10. Gastrointestinal Haemorrhage — 1 report (7.69%)

Source database →

Other Neuroscience approved in United States

Frequently asked questions

Is Neurodex approved in United States?

Yes. FDA has authorised it.

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

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