🇺🇸 Levetiracetam (Keppra) in United States

104 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. Immune Effector Cell-Associated Neurotoxicity Syndrome — 38 reports (36.54%)
  2. Cytokine Release Syndrome — 37 reports (35.58%)
  3. Neurotoxicity — 7 reports (6.73%)
  4. Delirium — 5 reports (4.81%)
  5. Convulsion — 4 reports (3.85%)
  6. Hypoxia — 3 reports (2.88%)
  7. Renal Failure — 3 reports (2.88%)
  8. Tachycardia — 3 reports (2.88%)
  9. Cerebrovascular Accident — 2 reports (1.92%)
  10. Decreased Appetite — 2 reports (1.92%)

Source database →

Other Neurology approved in United States

Frequently asked questions

Is Levetiracetam (Keppra) approved in United States?

Levetiracetam (Keppra) does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Levetiracetam (Keppra) in United States?

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