🇺🇸 Generic A in United States

6 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. Abdominal Pain Upper — 1 report (16.67%)
  2. Diarrhoea — 1 report (16.67%)
  3. Ill-Defined Disorder — 1 report (16.67%)
  4. Influenza Like Illness — 1 report (16.67%)
  5. Nausea — 1 report (16.67%)
  6. Vomiting — 1 report (16.67%)

Source database →

Generic A 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 Generic A approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Generic A in United States?

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