Reaction profile

The FDA adverse-event record for paralysis nos

363 FDA reports name paralysis nos, a high-volume reaction in the CVM extract (VeDDRA 1677). Plate stamps and neighbourhood peers follow.

#790 of 2,481
by report volume (all reactions)
363
reports citing this reaction
47.7%
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. Paralysis NOS has 363 reports now versus 344 in that prior snapshot: 19 more (5.5%).

Report change
+19
Death-coded reports
+11
Death-coded share
+0.6 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 Paralysis NOS changes

FDA AER · VeDDRA plate

Code 1677 VOL-LOW

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

  • VOL-LOW 363 reports
  • DEATH-HOT 47.7%
  • MID-PACK #790/2481
  • PHOTO-FINISH Gut sounds increased
  • SPECIES-DOG Dog · 307
  • DRUG-LEAD Bedinvetmab · 105
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Gut sounds increased (±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.

High-volume neighbourhood around Paralysis NOS

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

Vomiting · highest174348Gut sounds increased · near363Head pressing · near363Increased urine conce… · near363Lipoma · near363Paralysis NOS · this reaction363Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Paralysis NOS

Paralysis NOS: high death-coded share in the FDA AER plate

Signature read: 173 death-coded reports is a heavy tail count for Paralysis NOS in the CVM extract. Report volume is upper-third scale: 363 named reports in the openFDA extract. Death-coded share is upper-third: 173 of 363 reports (47.7% of named reports). Nearest volume peer: Gut sounds increased (±0 reports). Lead species Dog (307). Lead co-reported drug Bedinvetmab (105).

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 307
Cat 45
Cattle 3
Horse 3
Turkey 3
Pig 1
Rabbit 1

Breeds Most Affected

Retriever - Labrador 28
Domestic Shorthair 26
Dog (unknown) 26
Retriever - Golden 20
Shepherd Dog - German 20
Crossbred Canine/dog 16
Chihuahua 14
Shih Tzu 11
Siberian Husky 9
Terrier - Yorkshire 8

Associated Drugs

Bedinvetmab 105
Carprofen 40
Milbemycin Oxime + Spinosad 37
Pyrantel Pamoate;Sarolaner 26
Gabapentin 21
Afoxolaner 19
Maropitant Citrate 13
Cefovecin 12
Sarolaner 12
Frunevetmab 11
Spinosad 10
Oclacitinib Maleate 10
Prednisone 10
Fluralaner 13.64% 12-Week Chew 10
Nitenpyram 8
Fluralaner Chew Tablets 8
Metronidazole 8
Grapiprant 7
Meloxicam 6
Enrofloxacin 6

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Paralysis 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 report volume

Nearest other reactions by FDA report count (363 here).

Similar death-coded share

Nearest other reactions by death-coded share (47.7% 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 Paralysis NOS (#790 of 2,481 by report volume); death-coded 47.7%. PlainBreed reaction plate · death-coded report count stamp 173 · 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 →