Reaction profile

The FDA adverse-event record for hypercortisolaemia

86 FDA adverse-event reports reference hypercortisolaemia (VeDDRA 2624). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1470 of 2,481
by report volume (all reactions)
86
reports citing this reaction
26.7%
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. Hypercortisolaemia has 86 reports now versus 81 in that prior snapshot: 5 more (6.2%).

Report change
+5
Death-coded reports
+3
Death-coded share
+2.1 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 Hypercortisolaemia changes

FDA AER · VeDDRA plate

Code 2624 VOL-LOW

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

  • VOL-LOW 86 reports
  • DEATH-HOT 26.7%
  • MID-PACK #1470/2481
  • PHOTO-FINISH Alkalosis
  • SPECIES-DOG Dog · 83
  • DRUG-LEAD Carprofen · 21
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Alkalosis (±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.

Report-volume neighbourhood around Hypercortisolaemia

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

Vomiting · highest174348Alkalosis · near86Application site pust… · near86Conjunctival oedema · near86Eyelid inflammation · near86Hypercortisolaemia · this re…86Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Hypercortisolaemia

Hypercortisolaemia: high death-coded share in the FDA AER plate

Signature read: Hypercortisolaemia's 26.7% death-coded share is among the highest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is upper-third: 23 of 86 reports (26.7% of named reports). Nearest volume peer: Alkalosis (±0 reports). Lead species Dog (83). Lead co-reported drug Carprofen (21).

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 83
Cattle 2
Cat 1

Breeds Most Affected

Retriever - Golden 8
Retriever - Labrador 8
Poodle (unspecified) 4
Crossbred Canine/dog 4
Dachshund (unspecified) 3
Terrier - Yorkshire 3
Shepherd Dog - Australian 3
Maltese 3
Beagle 3
Shiba Inu 2

Associated Drugs

Carprofen 21
Oclacitinib Maleate 9
Ivermectin + Pyrantel As Pamoate Salt 9
Afoxolaner 8
Maropitant Citrate 8
Gabapentin 8
Isoflurane 8
Atipamezole 7
Dexmedetomidine 7
Enrofloxacin 5
Fluralaner 13.64% 12-Week Chew 5
Ondansetron 5
Maropitant 5
Butorphanol 5
Milbemycin Oxime + Spinosad 4
Meloxicam 4
Pantoprazole 4
Methadone 4
Fluralaner Chew Tablets 3
Grapiprant 3

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Hypercortisolaemia, 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 (86 here).

Similar death-coded share

Nearest other reactions by death-coded share (26.7% 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 Hypercortisolaemia (#1470 of 2,481 by report volume); death-coded 26.7%. PlainBreed reaction plate · death-coded share stamp 26.7% · 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 →