🇺🇸 Thioctic acid in United States

405 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. Drug Interaction — 62 reports (15.31%)
  2. Drug-Induced Liver Injury — 50 reports (12.35%)
  3. Hepatotoxicity — 43 reports (10.62%)
  4. Hepatic Cirrhosis — 41 reports (10.12%)
  5. Hepatic Encephalopathy — 40 reports (9.88%)
  6. Hepatic Necrosis — 40 reports (9.88%)
  7. Fatigue — 39 reports (9.63%)
  8. Diarrhoea — 32 reports (7.9%)
  9. Dyspnoea — 29 reports (7.16%)
  10. Nausea — 29 reports (7.16%)

Source database →

Frequently asked questions

Is Thioctic acid approved in United States?

Thioctic acid does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Thioctic acid in United States?

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