🇺🇸 TARTARIC ACID in United States

84 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. Off Label Use — 17 reports (20.24%)
  2. Drug Hypersensitivity — 15 reports (17.86%)
  3. Product Use In Unapproved Indication — 15 reports (17.86%)
  4. Toxic Epidermal Necrolysis — 15 reports (17.86%)
  5. Anaemia — 5 reports (5.95%)
  6. Arthralgia — 4 reports (4.76%)
  7. Fatigue — 4 reports (4.76%)
  8. Abdominal Distension — 3 reports (3.57%)
  9. Chest Pain — 3 reports (3.57%)
  10. Diarrhoea — 3 reports (3.57%)

Source database →

TARTARIC ACID in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is TARTARIC ACID approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for TARTARIC ACID in United States?

Marketing authorisation holder not available in our data.