Reaction profile

The FDA adverse-event record for fainting

165 FDA adverse-event reports reference fainting (VeDDRA 227). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1137 of 2,481
by report volume (all reactions)
165
reports citing this reaction
21.2%
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. Fainting has 165 reports now versus 163 in that prior snapshot: 2 more (1.2%).

Report change
+2
Death-coded reports
+2
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 Fainting changes

FDA AER · VeDDRA plate

Code 227 VOL-LOW

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

  • VOL-LOW 165 reports
  • DEATH-HOT 21.2%
  • MID-PACK #1137/2481
  • PHOTO-FINISH Low weight gain
  • SPECIES-DOG Dog · 147
  • DRUG-LEAD Pimobendan · 18
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Low weight gain (±0 reports)

Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.

Report-volume neighbourhood around Fainting

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

Vomiting · highest174348Fainting · this reaction165Low weight gain · near165Neuropathy NOS · near165Scaly condition NOS · near165Bronchopneumonia · near163Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Fainting

What the FDA AER plate says about Fainting

Signature read: 35 death-coded reports is the most distinctive absolute-outcome stamp on Fainting. Report volume sits in the middle third of the reaction corpus. 35 of 165 reports were death-coded (21.2% of named reports, not a population mortality rate). Nearest volume peer: Low weight gain (±0 reports). Lead species Dog (147). Lead co-reported drug Pimobendan (18).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Pimobendan 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 147
Human 9
Cat 7
Horse 2

Breeds Most Affected

Chihuahua 12
Retriever - Labrador 9
Unknown 9
Boxer (German Boxer) 9
Spitz - German Pomeranian 8
Dog (unknown) 5
Terrier - Yorkshire 5
Beagle 4
Poodle - Miniature 4
Schnauzer - Miniature 4

Associated Drugs

Pimobendan 18
Afoxolaner 16
Trilostane 14
Bedinvetmab 13
Milbemycin Oxime + Spinosad 11
Maropitant Citrate 9
Pyrantel Pamoate;Sarolaner 9
Enrofloxacin 8
Ivermectin + Pyrantel As Pamoate Salt 8
Oclacitinib Maleate 8
Gabapentin 7
Carprofen 6
Fluralaner Chew Tablets 6
Ivermectin 272Mcg, Pyrantel 227Mg 5
Moxidectin 5
Furosemide 5
Cefovecin 5
Galliprant 5
Dexamethasone 4
Spinosad 4

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Fainting, 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 (165 here).

Similar death-coded share

Nearest other reactions by death-coded share (21.2% 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 Fainting (#1137 of 2,481 by report volume); death-coded 21.2%. PlainBreed reaction plate · death-coded report count stamp 35 · 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 →