🇺🇸 Antioxidant formula in United States

22 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 — 4 reports (18.18%)
  2. Alopecia — 2 reports (9.09%)
  3. Arthralgia — 2 reports (9.09%)
  4. Death — 2 reports (9.09%)
  5. Fall — 2 reports (9.09%)
  6. Headache — 2 reports (9.09%)
  7. Malaise — 2 reports (9.09%)
  8. Product Dose Omission Issue — 2 reports (9.09%)
  9. Rectal Haemorrhage — 2 reports (9.09%)
  10. Weight Increased — 2 reports (9.09%)

Source database →

Antioxidant formula 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 Antioxidant formula approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Antioxidant formula in United States?

Bagcilar Training and Research Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.