Reaction profile
The FDA adverse-event record for anterior uveitis
93 FDA adverse-event reports reference anterior uveitis (VeDDRA 433). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.
- #1426 of 2,481
- by report volume (all reactions)
- 93
- reports citing this reaction
- 15.1%
- 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. Anterior uveitis has 93 reports now versus 93 in that prior snapshot: 0 the same number of (0.0%).
- Report change
- +0
- Death-coded reports
- +0
- Death-coded share
- −0.0 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 Anterior uveitis changesFDA AER · VeDDRA plate
Code 433 VOL-LOW
VOL-LOW · DEATH-ELEV · MID-PACK · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL
- VOL-LOW 93 reports
- DEATH-ELEV 15.1%
- MID-PACK #1426/2481
- PHOTO-FINISH Application site sero…
- SPECIES-DOG Dog · 73
- DRUG-LEAD Milbemycin Oxime… · 8
- DESK-WIDE 20 breeds
- BOOK-FULL 8/8 fields
Nearest volume peer: Application site serous discharge (±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.
Report-volume neighbourhood around Anterior uveitis
Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.
What the FDA AER plate says about Anterior uveitis
Signature read: report volume at 93 (#1426 of 2,481) is the standout scale stamp on Anterior uveitis. Report volume sits in the middle third of the reaction corpus. 14 of 93 reports were death-coded (15.1% of named reports, not a population mortality rate). Nearest volume peer: Application site serous discharge (±0 reports). Lead species Dog (73). Lead co-reported drug Milbemycin Oxime + Spinosad (8).
Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Milbemycin Oxime + Spinosad 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 Anterior uveitis, 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 (93 here).
Similar death-coded share
Nearest other reactions by death-coded share (15.1% here), distinct from the volume row.
What to do with this reaction
- Compare Anterior uveitis'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 →