Reaction profile

The FDA adverse-event record for spasm

413 FDA reports name spasm, a high-volume reaction in the CVM extract (VeDDRA 681). Plate stamps and neighbourhood peers follow.

#713 of 2,481
by report volume (all reactions)
413
reports citing this reaction
20.8%
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. Spasm has 413 reports now versus 409 in that prior snapshot: 4 more (1.0%).

Report change
+4
Death-coded reports
+2
Death-coded share
+0.3 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 Spasm changes

FDA AER · VeDDRA plate

Code 681 VOL-LOW

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

  • VOL-LOW 413 reports
  • DEATH-HOT 20.8%
  • MID-PACK #713/2481
  • PHOTO-FINISH Allergic dermatitis
  • SPECIES-DOG Dog · 301
  • DRUG-LEAD Sarolaner · 25
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Allergic dermatitis (±1 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 Spasm

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

Vomiting · highest174348Allergic dermatitis · near414Incorrect storage of… · near414Urinary retention · near414Spasm · this reaction413Coagulopathy · near412Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Spasm

What the FDA AER plate says about Spasm

Signature read: 86 death-coded reports is a heavy tail count for Spasm in the CVM extract. Report volume is upper-third scale: 413 named reports in the openFDA extract. 86 of 413 reports were death-coded (20.8% of named reports, not a population mortality rate). Nearest volume peer: Allergic dermatitis (±1 reports). Lead species Dog (301). Lead co-reported drug Sarolaner (25).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Sarolaner 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 301
Cat 73
Horse 24
Cattle 3
Human 3
Rabbit 3
Other 2
Mouse 1
Bison 1
Sheep 1

Breeds Most Affected

Crossbred Canine/dog 39
Domestic (unspecified) 22
Retriever - Labrador 22
Dog (unknown) 19
Chihuahua 18
Terrier - Yorkshire 16
Shih Tzu 14
Cat (unknown) 14
Retriever - Golden 14
Domestic Shorthair 14

Associated Drugs

Sarolaner 25
Afoxolaner 24
Spinosad 23
Milbemycin Oxime + Spinosad 23
Ketamine Hydrochloride 21
Propofol 19
Selamectin 18
Maropitant Citrate 18
Pyrantel Pamoate;Sarolaner 17
Bedinvetmab 16
Gabapentin 14
Meloxicam 13
Fluralaner Chew Tablets 12
Ivermectin + Pyrantel As Pamoate Salt 10
Carprofen 9
Enrofloxacin 8
Fluralaner 13.64% 12-Week Chew 8
Frunevetmab 8
Ivermectin, Pyrantel 7
Tiletamine, Zolazepam 7

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Spasm, 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 (413 here).

Similar death-coded share

Nearest other reactions by death-coded share (20.8% 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 Spasm (#713 of 2,481 by report volume); death-coded 20.8%. PlainBreed reaction plate · death-coded report count stamp 86 · 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 →