🇺🇸 E2007 (perampanel) in United States

39 US adverse-event reports

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 — 6 reports (15.38%)
  2. Status Epilepticus — 6 reports (15.38%)
  3. Aggression — 5 reports (12.82%)
  4. Acute Psychosis — 4 reports (10.26%)
  5. Contusion — 3 reports (7.69%)
  6. Grand Mal Convulsion — 3 reports (7.69%)
  7. Headache — 3 reports (7.69%)
  8. Nausea — 3 reports (7.69%)
  9. Pneumonia — 3 reports (7.69%)
  10. Urinary Tract Infection — 3 reports (7.69%)

Source database →

Other Neurology approved in United States

Frequently asked questions

Is E2007 (perampanel) approved in United States?

E2007 (perampanel) does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for E2007 (perampanel) in United States?

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