🇺🇸 Byetta (Exenatide) in United States

177 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. Blood Glucose Increased — 36 reports (20.34%)
  2. Nausea — 23 reports (12.99%)
  3. Weight Decreased — 19 reports (10.73%)
  4. Bladder Cancer — 17 reports (9.6%)
  5. Blood Glucose Decreased — 16 reports (9.04%)
  6. Pancreatitis — 15 reports (8.47%)
  7. Pancreatitis Acute — 14 reports (7.91%)
  8. Renal Failure — 14 reports (7.91%)
  9. Malaise — 12 reports (6.78%)
  10. Vomiting — 11 reports (6.21%)

Source database →

Other Diabetes approved in United States

Frequently asked questions

Is Byetta (Exenatide) approved in United States?

Byetta (Exenatide) does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Byetta (Exenatide) in United States?

Beijing Chao Yang Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.