Reaction profile

The FDA adverse-event record for bounding pulse

50 FDA reports name bounding pulse, a lower-volume reaction in the CVM extract (VeDDRA 2522). Plate stamps and neighbourhood peers follow.

#1735 of 2,481
by report volume (all reactions)
50
reports citing this reaction
42.0%
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. Bounding pulse has 50 reports now versus 50 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 Bounding pulse changes

FDA AER · VeDDRA plate

Code 2522 VOL-LOW

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

  • VOL-LOW 50 reports
  • DEATH-HOT 42.0%
  • MID-PACK #1735/2481
  • PHOTO-FINISH Application site papu…
  • SPECIES-DOG Dog · 44
  • DRUG-LEAD Maropitant Citrate · 12
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Application site papule (±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.

Lower-volume neighbourhood around Bounding pulse

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

Vomiting · highest174348Application site papu… · near50Bounding pulse · this reacti…50Device-related infect… · near50Eyeball protrusion · near50Lymphadenitis · near50Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Bounding pulse

Bounding pulse: high death-coded share in the FDA AER plate

Signature read: Bounding pulse's 42.0% death-coded share is among the highest in the openFDA reaction corpus. Report volume is lower-third scale: 50 named reports in the openFDA extract. Death-coded share is upper-third: 21 of 50 reports (42.0% of named reports). Nearest volume peer: Application site papule (±0 reports). Lead species Dog (44). Lead co-reported drug Maropitant Citrate (12).

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 44
Cat 5
Horse 1

Breeds Most Affected

Retriever - Labrador 6
Domestic Shorthair 4
Boxer (German Boxer) 3
Shepherd Dog - German 2
Bichon Frise 2
Corgi (unspecified) 2
Maltese 2
Pit Bull 2
Spaniel - Springer English 2
Chihuahua 2

Associated Drugs

Maropitant Citrate 12
Gabapentin 12
Carprofen 11
Enrofloxacin 6
Bedinvetmab 6
Sarolaner 5
Isoflurane 5
Moxidectin 5
Midazolam 5
Doxycycline 4
Galliprant 4
Prednisone 3
Mirtazapine 3
Melarsomine Dihydrochloride 3
Buprenorphine 3
Trilostane 3
Milbemycin Oxime + Praziquantel 3
Lotilaner 3
Dexmedetomidine 3
Fluid Therapy 3

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Bounding pulse, 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 (50 here).

Similar death-coded share

Nearest other reactions by death-coded share (42.0% 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 Bounding pulse (#1735 of 2,481 by report volume); death-coded 42.0%. PlainBreed reaction plate · death-coded share stamp 42.0% · 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 →