Reaction profile
The FDA adverse-event record for periorbital oedema (see also immune system disorders)
13 FDA reports name periorbital oedema (see also immune system disorders), a lower-volume reaction in the CVM extract (VeDDRA 460). Plate stamps and neighbourhood peers follow.
- #2366 of 2,481
- by report volume (all reactions)
- 13
- reports citing this reaction
- 0.0%
- death-coded share
- Dog
- most-affected species
FDA AER · VeDDRA plate
Code 460 VOL-TRACE
VOL-TRACE · DEATH-RARE · BOTTOM-DECILE · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL
- VOL-TRACE 13 reports
- DEATH-RARE 0.0%
- BOTTOM-DECILE #2366/2481
- PHOTO-FINISH Abnormal digital pulse
- SPECIES-DOG Dog · 12
- DRUG-LEAD Moxidectin · 4
- DESK-WIDE 11 breeds
- BOOK-FULL 8/8 fields
Nearest volume peer: Abnormal digital pulse (±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 Periorbital oedema
Lower-third volume poles plus nearest peers, not a full reaction corpus board reprint.
Periorbital oedema (see also Immune system disorders): low death-coded share in the FDA AER plate
Signature read: 13 reports place Periorbital oedema (see also Immune system disorders) in the lower third of FDA AER volume (#2366 of 2,481). Report volume is lower-third scale: 13 named reports in the openFDA extract. Death-coded share is lower-third: 0 of 13 reports (0.0% of named reports). Nearest volume peer: Abnormal digital pulse (±0 reports). Lead species Dog (12). Lead co-reported drug Moxidectin (4).
Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Moxidectin 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
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 →