Safety

TB-500

Adverse-event report summary for TB-500, drawn from the FDA Adverse Event Reporting System (FAERS).

Total reports
1
Reports flagged serious
1

“Serious” is FAERS’s own report-level flag (e.g. death, hospitalization, or another outcome the reporter marked as serious) and does not indicate a verified or compound-caused outcome.

Most frequently reported reactions

  1. Adverse Drug Reaction1 reports
  2. Malignant Lymphoid Neoplasm1 reports
  3. Product Dispensed By Unauthorised Provider1 reports

Counts reflect the most-reported reaction terms (MedDRA preferred terms) associated with reports naming this compound. A single report can list multiple reactions, so reaction counts need not sum to the total number of reports.