Reaction profile

The FDA adverse-event record for high blood pressure

599 FDA reports name high blood pressure, a high-volume reaction in the CVM extract (VeDDRA 225). Plate stamps and neighbourhood peers follow.

#574 of 2,481
by report volume (all reactions)
599
reports citing this reaction
13.0%
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. High blood pressure has 599 reports now versus 585 in that prior snapshot: 14 more (2.4%).

Report change
+14
Death-coded reports
+0
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 High blood pressure changes

FDA AER · VeDDRA plate

Code 225 VOL-MID

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

  • VOL-MID 599 reports
  • DEATH-ELEV 13.0%
  • UPPER-Q #574/2481
  • PHOTO-FINISH Hair change
  • SPECIES-DOG Dog · 430
  • DRUG-LEAD Trilostane · 85
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Hair change (±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 High blood pressure

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

Vomiting · highest174348Soft stool · near601High blood pressure · this r…599Hair change · near598Neurological disorder… · near597Enlarged lymph node (… · near594Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around High blood pressure

What the FDA AER plate says about High blood pressure

Signature read: 78 death-coded reports is a heavy tail count for High blood pressure in the CVM extract. Report volume is upper-third scale: 599 named reports in the openFDA extract. 78 of 599 reports were death-coded (13.0% of named reports, not a population mortality rate). Nearest volume peer: Hair change (±1 reports). Lead species Dog (430). Lead co-reported drug Trilostane (85).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Trilostane 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 430
Cat 116
Human 52
Cattle 1

Breeds Most Affected

Domestic Shorthair 75
Unknown 53
Retriever - Labrador 44
Crossbred Canine/dog 29
Chihuahua 22
Terrier - Yorkshire 20
Shih Tzu 20
Beagle 16
Retriever - Golden 13
Dachshund (unspecified) 11

Associated Drugs

Trilostane 85
Bedinvetmab 55
Milbemycin Oxime + Spinosad 41
Maropitant Citrate 39
Gabapentin 38
Carprofen 33
Phenylpropropanolamine Hcl 25
Prednisone 24
Grapiprant 23
Buprenorphine 20
Frunevetmab 20
Butorphanol 19
Amlodipine 18
Pimobendan 17
Moxidectin 16
Tilmicosin 16
Milbemycin Oxime + Praziquantel 16
Pyrantel Pamoate;Sarolaner 16
Benazepril 15
Robenacoxib 15

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for High blood pressure, 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 (599 here).

Similar death-coded share

Nearest other reactions by death-coded share (13.0% 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 High blood pressure (#574 of 2,481 by report volume); death-coded 13.0%. PlainBreed reaction plate · death-coded report count stamp 78 · 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 →