🇺🇸 Centella in United States

194 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. Cerebral Venous Thrombosis — 31 reports (15.98%)
  2. Drug Interaction — 27 reports (13.92%)
  3. Product Use In Unapproved Indication — 22 reports (11.34%)
  4. Headache — 20 reports (10.31%)
  5. Thalamic Infarction — 20 reports (10.31%)
  6. Fatigue — 19 reports (9.79%)
  7. Intentional Product Misuse — 16 reports (8.25%)
  8. Bradyphrenia — 15 reports (7.73%)
  9. Off Label Use — 12 reports (6.19%)
  10. Slow Response To Stimuli — 12 reports (6.19%)

Source database →

Other Other approved in United States

Frequently asked questions

Is Centella approved in United States?

Yes. FDA has authorised it.

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

University of Roma La Sapienza is the originator. The local marketing authorisation holder may differ — check the official source linked above.