Reaction profile

The FDA adverse-event record for pr-neoplasia

65 FDA adverse-event reports reference pr-neoplasia (VeDDRA 99936). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1616 of 2,481
by report volume (all reactions)
65
reports citing this reaction
69.2%
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. PR-NEOPLASIA has 65 reports now versus 65 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 PR-NEOPLASIA changes

FDA AER · VeDDRA plate

Code 99936 VOL-LOW

VOL-LOW · DEATH-HOT · MID-PACK · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-LOW 65 reports
  • DEATH-HOT 69.2%
  • MID-PACK #1616/2481
  • PHOTO-FINISH Acne
  • SPECIES-DOG Dog · 47
  • DRUG-LEAD Oclacitinib Malea… · 22
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Acne (±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.

Report-volume neighbourhood around PR-NEOPLASIA

Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.

Vomiting · highest174348Acne · near65Gut sounds decreased · near65Hair standing on end · near65Immune-mediated polya… · near65PR-NEOPLASIA · this reaction65Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around PR-NEOPLASIA

PR-NEOPLASIA: high death-coded share in the FDA AER plate

Signature read: PR-NEOPLASIA's 69.2% death-coded share is among the highest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is upper-third: 45 of 65 reports (69.2% of named reports). Nearest volume peer: Acne (±0 reports). Lead species Dog (47). Lead co-reported drug Oclacitinib Maleate (22).

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

Dog 47
Cat 17
Horse 1

Breeds Most Affected

Domestic Shorthair 8
Retriever - Labrador 8
Retriever - Golden 6
Shih Tzu 4
Domestic Longhair 4
Shepherd Dog - German 3
Retriever (unspecified) 2
Schnauzer (unspecified) 2
Beagle 2
Cat (unknown) 1

Associated Drugs

Oclacitinib Maleate 22
Cefovecin 12
Moxidectin 6
Carprofen 4
Spinosad 3
Anesthetic 3
Maropitant Citrate 3
Cyclosporine A 3
Cyclosporine 3
Enrofloxacin 3
Cefpodoxime Proxetil 3
Fluralaner Chew Tablets 3
Phenylpropanolamine 2
Milbemycin Oxime + Spinosad 2
Acepromazine Maleate 2
Sevoflurane 2
Imidacloprid + Moxidectin 2
Propofol 2
Methylprednisolone Acetate 2
Buprenorphine 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for PR-NEOPLASIA, 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 (65 here).

Similar death-coded share

Nearest other reactions by death-coded share (69.2% here), distinct from the volume row.

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 PR-NEOPLASIA (#1616 of 2,481 by report volume); death-coded 69.2%. PlainBreed reaction plate · death-coded share stamp 69.2% · 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 →