Reaction profile
The FDA adverse-event record for epistaxis (unilateral)
57 FDA reports name epistaxis (unilateral), a lower-volume reaction in the CVM extract (VeDDRA 2485). Plate stamps and neighbourhood peers follow.
- #1672 of 2,481
- by report volume (all reactions)
- 57
- reports citing this reaction
- 10.5%
- death-coded share
- Dog
- most-affected species
Release-over-release change
What changed in the latest FDA data snapshot
PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Epistaxis (unilateral) has 57 reports now versus 55 in that prior snapshot: 2 more (3.6%).
- Report change
- +2
- Death-coded reports
- +0
- Death-coded share
- −0.4 pts
This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.
Subscribe to Epistaxis (unilateral) changesFDA AER · VeDDRA plate
Code 2485 VOL-LOW
VOL-LOW · DEATH-ELEV · MID-PACK · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL
- VOL-LOW 57 reports
- DEATH-ELEV 10.5%
- MID-PACK #1672/2481
- PHOTO-FINISH Atrial fibrillation
- SPECIES-DOG Dog · 49
- DRUG-LEAD Bedinvetmab · 9
- DESK-WIDE 20 breeds
- BOOK-FULL 8/8 fields
Nearest volume peer: Atrial fibrillation (±0 reports)
Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.
Lower-volume neighbourhood around Epistaxis
Lower-third volume poles plus nearest peers, not a full reaction corpus board reprint.
What the FDA AER plate says about Epistaxis (unilateral)
Signature read: 6 death-coded reports is a thin tail count for Epistaxis (unilateral) in the CVM extract. Report volume is lower-third scale: 57 named reports in the openFDA extract. 6 of 57 reports were death-coded (10.5% of named reports, not a population mortality rate). Nearest volume peer: Atrial fibrillation (±0 reports). Lead species Dog (49). Lead co-reported drug Bedinvetmab (9).
Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Bedinvetmab appears in filings alongside this reaction; that is association, not causation. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.
Species Most Affected
Breeds Most Affected
Associated Drugs
Nationwide reactions with similar profiles
Two openFDA-derived peer sets for Epistaxis (unilateral), both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).
Similar report volume
Nearest other reactions by FDA report count (57 here).
Similar death-coded share
Nearest other reactions by death-coded share (10.5% here), distinct from the volume row.
What to do with this reaction
- Compare Epistaxis's report profile against similar reactions nationwide. See similar reactions
- 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 →