Reaction profile

The FDA adverse-event record for excitation

379 FDA reports name excitation, a high-volume reaction in the CVM extract (VeDDRA 120). Plate stamps and neighbourhood peers follow.

#756 of 2,481
by report volume (all reactions)
379
reports citing this reaction
11.3%
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. Excitation has 379 reports now versus 373 in that prior snapshot: 6 more (1.6%).

Report change
+6
Death-coded reports
+0
Death-coded share
−0.2 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 Excitation changes

FDA AER · VeDDRA plate

Code 120 VOL-LOW

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

  • VOL-LOW 379 reports
  • DEATH-ELEV 11.3%
  • MID-PACK #756/2481
  • PHOTO-FINISH Skin petechiae
  • SPECIES-DOG Dog · 242
  • DRUG-LEAD Buprenorphine · 72
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Skin petechiae (±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 Excitation

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

Vomiting · highest174348Excitation · this reaction379Skin petechiae · near379Increased drinking · near378Pinnal oedema · near378Respiratory sound · near378Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Excitation

What the FDA AER plate says about Excitation

Signature read: 379 reports place Excitation in the upper third of FDA AER volume (#756 of 2,481). Report volume is upper-third scale: 379 named reports in the openFDA extract. 43 of 379 reports were death-coded (11.3% of named reports, not a population mortality rate). Nearest volume peer: Skin petechiae (±0 reports). Lead species Dog (242). Lead co-reported drug Buprenorphine (72).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Buprenorphine 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 242
Cat 116
Horse 18
Other Rodents 1
Mouse 1
Cattle 1

Breeds Most Affected

Domestic Shorthair 61
Dog (unknown) 25
Retriever - Labrador 24
Crossbred Canine/dog 17
Cat (unknown) 14
Unknown 14
Shepherd Dog - German 10
Terrier - Yorkshire 10
Retriever - Golden 9
Boxer (German Boxer) 8

Associated Drugs

Buprenorphine 72
Milbemycin Oxime + Spinosad 39
Isoflurane 33
Alfaxalone 32
Propofol 26
Butorphanol 26
Dexmedetomidine 23
Ketamine 15
Maropitant Citrate 14
Midazolam 13
Acepromazine 13
Carprofen 12
Dexmedetomidine Hydrochloride 12
Atipamezole Hydrochloride 12
Oclacitinib Maleate 12
Spinosad 11
Trilostane 11
Nitenpyram 11
Robenacoxib 11
Pyrantel Pamoate;Sarolaner 10

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Excitation, 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 (379 here).

Similar death-coded share

Nearest other reactions by death-coded share (11.3% 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 Excitation (#756 of 2,481 by report volume); death-coded 11.3%. PlainBreed reaction plate · report volume stamp 379 · 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 →