fda adverse event
Entity, reached from Hormuz.
- Evidence
- 22 documents · 2 separate publishers
- Standing
- Added automatically from coverage
- Time
- first seen 6 Apr 2026, last seen 9 Oct 2026
- Measured
- 91% of mentions say something specific about it; the rest only name it
- As of
- 10 Oct 2026
Where this comes from
- FDA · 2026-10-01 · FDA Adverse Event Monitoring System (AEMS) – E2B(R3) Data Standards (opens the source in a new tab)
- FDA · 2026-10-01 · FDA Adverse Event Monitoring System (AEMS) Electronic Submissions (opens the source in a new tab)
- FDA Drug News · 2026-07-01 · January - March 2026 | New Safety Information or Potential Signals of Serious Risks Identified by the FDA Adverse Event Monitoring System (AEMS) (opens the source in a new tab)
- FDA Drug News · 2026-06-13 · October - December 2024 | New Safety Information or Potential Signals of Serious Risks Identified from the FDA Adverse Event Monitoring System (AEMS) (opens the source in a new tab)
- FDA Drug News · 2026-06-13 · October - December 2022 | New Safety Information or Potential Signals of Serious Risks Identified from the FDA Adverse Event Monitoring System (AEMS) (opens the source in a new tab)
- FDA Drug News · 2026-06-13 · July - September 2022 | New Safety Information or Potential Signals of Serious Risks Identified from the FDA Adverse Event Monitoring System (AEMS) (opens the source in a new tab)
- FDA Drug News · 2026-06-13 · January - March 2024 | New Safety Information or Potential Signals of Serious Risks Identified from the FDA Adverse Event Monitoring System (AEMS) (opens the source in a new tab)
- FDA Drug News · 2026-06-13 · January - March 2022 | New Safety Information or Potential Signals of Serious Risks Identified from the FDA Adverse Event Monitoring System (AEMS) (opens the source in a new tab)
- FDA Drug News · 2026-06-13 · April - June 2022 | New Safety Information or Potential Signals of Serious Risks Identified from the FDA Adverse Event Monitoring System (AEMS) (opens the source in a new tab)
- FDA Drug News · 2026-04-17 · Electronic Submission of Adverse Event Reports to FDA Adverse Event Reporting System (FAERS) using International Council for Harmonisation (ICH) E2B(R3) Standards - 04/04… (opens the source in a new tab)
2 more on file, counted in the evidence above.
What is claimed about it
Situations it is named in
Who it moves with
- co-mentioned with fda (22 documents)seen together
- co-mentioned with faers (13 documents)seen together
- co-mentioned with reporting system (13 documents)seen together
- co-mentioned with aems (12 documents)seen together
- co-mentioned with monitoring system (12 documents)seen together