Reaction profile

The FDA adverse-event record for hypoadrenocorticism

768 FDA reports name hypoadrenocorticism, a high-volume reaction in the CVM extract (VeDDRA 383). Plate stamps and neighbourhood peers follow.

#475 of 2,481
by report volume (all reactions)
768
reports citing this reaction
7.3%
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. Hypoadrenocorticism has 768 reports now versus 768 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 Hypoadrenocorticism changes

FDA AER · VeDDRA plate

Code 383 VOL-MID

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

  • VOL-MID 768 reports
  • DEATH-PAR 7.3%
  • UPPER-Q #475/2481
  • PHOTO-FINISH Crystalluria
  • SPECIES-DOG Dog · 766
  • DRUG-LEAD Trilostane · 1,090
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Crystalluria (±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 Hypoadrenocorticism

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

Vomiting · highest174348Diabetes mellitus · near770Quiet · near770Crystalluria · near769Hypoadrenocorticism · this r…768Application site swel… · near764Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Hypoadrenocorticism

Hypoadrenocorticism: low death-coded share in the FDA AER plate

Signature read: 768 reports place Hypoadrenocorticism in the upper third of FDA AER volume (#475 of 2,481). Report volume is upper-third scale: 768 named reports in the openFDA extract. Death-coded share is lower-third: 56 of 768 reports (7.3% of named reports). Nearest volume peer: Crystalluria (±1 reports). Lead species Dog (766). Lead co-reported drug Trilostane (1,090).

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 766
Human 1
Cat 1

Breeds Most Affected

Retriever - Labrador 72
Terrier - Boston 44
Crossbred Canine/dog 40
Maltese 36
Boxer (German Boxer) 35
Spaniel (unspecified) 27
Shih Tzu 24
American Pit Bull Terrier 24
Dog (unknown) 21
Chihuahua 21

Associated Drugs

Trilostane 1,090
Carprofen 34
Milbemycin Oxime + Spinosad 19
Levothyroxine 19
Oclacitinib Maleate 19
Gabapentin 16
Insulin 14
Ursodiol 11
Prednisone 10
Grapiprant 10
Amlodipine 9
Metronidazole 8
Maropitant Citrate 8
Compounded Trilostane 7
Polysulfated Glycosaminoglycan 7
Pimobendan 7
Cyclosporine 6
Benazapril 6
Mitotane 6
Benazepril 6

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Hypoadrenocorticism, 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 (768 here).

Similar death-coded share

Nearest other reactions by death-coded share (7.3% 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 Hypoadrenocorticism (#475 of 2,481 by report volume); death-coded 7.3%. PlainBreed reaction plate · report volume stamp 768 · 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 →