Reaction profile

The FDA adverse-event record for pancreatitis nos

760 FDA reports name pancreatitis nos, a high-volume reaction in the CVM extract (VeDDRA 1891). Plate stamps and neighbourhood peers follow.

#482 of 2,481
by report volume (all reactions)
760
reports citing this reaction
23.0%
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. Pancreatitis NOS has 760 reports now versus 699 in that prior snapshot: 61 more (8.7%).

Report change
+61
Death-coded reports
+7
Death-coded share
−1.0 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 Pancreatitis NOS changes

FDA AER · VeDDRA plate

Code 1891 VOL-MID

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

  • VOL-MID 760 reports
  • DEATH-HOT 23.0%
  • UPPER-Q #482/2481
  • PHOTO-FINISH Decreased body temper…
  • SPECIES-DOG Dog · 549
  • DRUG-LEAD Bedinvetmab · 182
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Decreased body temperature (±0 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 Pancreatitis NOS

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

Vomiting · highest174348Colic · near762INEFFECTIVE, GASTRIC… · near762Decreased body temper… · near760Pancreatitis NOS · this reac…760General pain (see oth… · near758Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Pancreatitis NOS

What the FDA AER plate says about Pancreatitis NOS

Signature read: 175 death-coded reports is a heavy tail count for Pancreatitis NOS in the CVM extract. Report volume is upper-third scale: 760 named reports in the openFDA extract. 175 of 760 reports were death-coded (23.0% of named reports, not a population mortality rate). Nearest volume peer: Decreased body temperature (±0 reports). Lead species Dog (549). Lead co-reported drug Bedinvetmab (182).

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

Dog 549
Cat 211

Breeds Most Affected

Domestic Shorthair 125
Crossbred Canine/dog 44
Retriever - Labrador 39
Terrier - Yorkshire 33
Domestic Longhair 25
Retriever - Golden 24
Dog (unknown) 22
Chihuahua 17
Shepherd Dog - Australian 17
Shih Tzu 16

Associated Drugs

Bedinvetmab 182
Maropitant Citrate 134
Gabapentin 85
Bexagliflozin 60
Velagliflozin Proline Monohydrate 55
Trilostane 53
Oclacitinib Maleate 46
Frunevetmab 44
Pyrantel Pamoate;Sarolaner 38
Carprofen 36
Fluid Therapy 35
Ondansetron 35
Fluralaner 13.64% 12-Week Chew 32
Prednisone 32
Metronidazole 31
Buprenorphine 28
Enrofloxacin 27
Afoxolaner 24
Anti-Il31 Mab Mcs Lot #1283563 22
Trazodone 20

Nationwide reactions with similar profiles

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

Similar death-coded share

Nearest other reactions by death-coded share (23.0% 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 Pancreatitis NOS (#482 of 2,481 by report volume); death-coded 23.0%. PlainBreed reaction plate · death-coded report count stamp 175 · 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 →