Reaction profile
The FDA adverse-event record for elevated serum amyloid a (saa)
13 FDA reports name elevated serum amyloid a (saa), a lower-volume reaction in the CVM extract (VeDDRA 3179). Plate stamps and neighbourhood peers follow.
- #2352 of 2,481
- by report volume (all reactions)
- 13
- reports citing this reaction
- 30.8%
- death-coded share
- Horse
- most-affected species
FDA AER · VeDDRA plate
Code 3179 VOL-TRACE
VOL-TRACE · DEATH-HOT · BOTTOM-DECILE · PHOTO-FINISH · SPECIES-HORSE · DRUG-LEAD · DESK-WIDE · BOOK-FULL
- VOL-TRACE 13 reports
- DEATH-HOT 30.8%
- BOTTOM-DECILE #2352/2481
- PHOTO-FINISH Abnormal digital pulse
- SPECIES-HORSE Horse · 13
- DRUG-LEAD Flunixin Meglumin… · 3
- DESK-WIDE 9 breeds
- BOOK-FULL 8/8 fields
Nearest volume peer: Abnormal digital pulse (±0 reports)
Upper-third death-coded share drives the outcome stamps on this plate; volume band, corpus rank, and co-report peers follow. Not a clinical diagnosis.
Lower-volume neighbourhood around Elevated serum amyloid A
Lower-third volume poles plus nearest peers, not a full reaction corpus board reprint.
Elevated serum amyloid A (SAA): high death-coded share in the FDA AER plate
Signature read: 13 reports place Elevated serum amyloid A (SAA) in the lower third of FDA AER volume (#2352 of 2,481). Report volume is lower-third scale: 13 named reports in the openFDA extract. Death-coded share is upper-third: 4 of 13 reports (30.8% of named reports). Nearest volume peer: Abnormal digital pulse (±0 reports). Lead species Horse (13). Lead co-reported drug Flunixin Meglumine Injectable (3).
Read these counts as reporting volume, not risk: per our methodology, A high death-coded share in FDA filings does not prove causation; co-reporting is voluntary temporal association only. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.
Species Most Affected
Breeds Most Affected
Associated Drugs
What to do with this reaction
- Read how death-coded share differs from a mortality rate before drawing conclusions. Understanding adverse events
- Browse the full reaction directory to compare report counts across reaction types. All reactions
A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.
Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025
Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →