Reaction profile

The FDA adverse-event record for contamination, particulate matter

731 FDA reports name contamination, particulate matter, a high-volume reaction in the CVM extract (VeDDRA 99846). Plate stamps and neighbourhood peers follow.

#488 of 2,481
by report volume (all reactions)
731
reports citing this reaction
0.4%
death-coded share
Unknown
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. Contamination, Particulate Matter has 731 reports now versus 718 in that prior snapshot: 13 more (1.8%).

Report change
+13
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 Contamination, Particulate Matter changes

FDA AER · VeDDRA plate

Code 99846 VOL-MID

VOL-MID · DEATH-RARE · UPPER-Q · PHOTO-FINISH · SPECIES-UNKNOWN · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-MID 731 reports
  • DEATH-RARE 0.4%
  • UPPER-Q #488/2481
  • PHOTO-FINISH Application site pain
  • SPECIES-UNKNOWN Unknown · 709
  • DRUG-LEAD Moxidectin · 123
  • DESK-WIDE 14 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Application site pain (±2 reports)

Upper-third report volume drives the scale stamps on this plate; death-coded share and co-report peers follow. Not a clinical diagnosis.

High-volume neighbourhood around Contamination, Particulate Matter

Upper-third volume poles plus nearest peers, not a full reaction corpus board reprint.

Vomiting · highest174348Chewing - pruritus (s… · near735Contamination, Partic… · thi…731Application site pain · near729Generalised weakness · near729Swollen limb · near729Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Contamination, Particulate Matter

Contamination, Particulate Matter: low death-coded share in the FDA AER plate

Signature read: Contamination, Particulate Matter's 0.4% death-coded share is among the lowest in the openFDA reaction corpus. Report volume is upper-third scale: 731 named reports in the openFDA extract. Death-coded share is lower-third: 3 of 731 reports (0.4% of named reports). Nearest volume peer: Application site pain (±2 reports). Lead species Unknown (709). Lead co-reported drug Moxidectin (123).

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

Unknown 709
Dog 18
Cat 4

Breeds Most Affected

Unknown 712
Crossbred Canine/dog 4
Dog (unknown) 3
Retriever - Labrador 2
Hound (unspecified) 1
Cat (unknown) 1
Bichon Frise 1
Siamese 1
Spitz - American Eskimo Dog 1
Terrier - West Highland White 1

Associated Drugs

Moxidectin 123
Insulin Injectable Vial 96
Cefovecin 48
Enrofloxacin 35
Amprolium 34
Flunixin Meglumine Injectable 29
Propofol 27
Maropitant Citrate 21
Triamcinolone Acetonide 18
Hyaluronate Sodium 18
Carprofen 16
Furosemide Injection 15
Butorphanol Injectable 12
Polysulfated Glycosaminoglycan 9
Meloxicam 9
Robenacoxib 9
Ceftiofur Sodium 8
Bupivacaine 8
Maropitant 7
Amprolium Ion 6

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Contamination, Particulate Matter, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).

What to do with this reaction

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

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Contamination, Particulate Matter (#488 of 2,481 by report volume); death-coded 0.4%. PlainBreed reaction plate · death-coded share stamp 0.4% · vintage 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 →