🇺🇸 FORODESINE HYDROCHLORIDE in United States

41 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. Malignant Neoplasm Progression — 13 reports (31.71%)
  2. Neutrophil Count Decreased — 4 reports (9.76%)
  3. Stomatitis — 4 reports (9.76%)
  4. Blood Lactate Dehydrogenase Increased — 3 reports (7.32%)
  5. Death — 3 reports (7.32%)
  6. Lymphopenia — 3 reports (7.32%)
  7. Malaise — 3 reports (7.32%)
  8. Platelet Count Decreased — 3 reports (7.32%)
  9. White Blood Cell Count Decreased — 3 reports (7.32%)
  10. Alanine Aminotransferase Increased — 2 reports (4.88%)

Source database →

FORODESINE HYDROCHLORIDE 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 FORODESINE HYDROCHLORIDE approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for FORODESINE HYDROCHLORIDE in United States?

Marketing authorisation holder not available in our data.