Reaction profile

The FDA adverse-event record for endocrine system disorder nos

18 FDA reports name endocrine system disorder nos, a lower-volume reaction in the CVM extract (VeDDRA 2014). Plate stamps and neighbourhood peers follow.

#2206 of 2,481
by report volume (all reactions)
18
reports citing this reaction
11.1%
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. Endocrine system disorder NOS has 18 reports now versus 18 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 Endocrine system disorder NOS changes

FDA AER · VeDDRA plate

Code 2014 VOL-TRACE

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

  • VOL-TRACE 18 reports
  • DEATH-ELEV 11.1%
  • LOWER-Q #2206/2481
  • PHOTO-FINISH ALBUMIN/GLOBULIN RATI…
  • SPECIES-DOG Dog · 14
  • DRUG-LEAD Ivermectin + Pyra… · 4
  • DESK-WIDE 15 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: ALBUMIN/GLOBULIN RATIO HI, BLD (±0 reports)

Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.

Lower-volume neighbourhood around Endocrine system disorder NOS

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

Vomiting · highest174348ALBUMIN/GLOBULIN RATI… · near18Application site skin… · near18Bone marrow hypoplasia · near18Cognitive disturbance · near18Endocrine system diso… · thi…18Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Endocrine system disorder NOS

What the FDA AER plate says about Endocrine system disorder NOS

Signature read: 18 reports place Endocrine system disorder NOS in the lower third of FDA AER volume (#2206 of 2,481). Report volume is lower-third scale: 18 named reports in the openFDA extract. 2 of 18 reports were death-coded (11.1% of named reports, not a population mortality rate). Nearest volume peer: ALBUMIN/GLOBULIN RATIO HI, BLD (±0 reports). Lead species Dog (14). Lead co-reported drug Ivermectin + Pyrantel As Pamoate Salt (4).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Ivermectin + Pyrantel As Pamoate Salt 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 14
Cat 2
Pig 1
Human 1

Breeds Most Affected

Dog (unknown) 4
Retriever - Chesapeake Bay 1
Bulldog 1
Spaniel - King Charles Cavalier 1
Crossbred Porcine/Pig 1
Boxer (German Boxer) 1
Pinscher - Miniature 1
Corgi - Welsh Pembroke 1
Unknown 1
Pug 1

Associated Drugs

Ivermectin + Pyrantel As Pamoate Salt 4
Milbemycin Oxime + Spinosad 3
Oclacitinib Maleate 3
Spinosad 2
Gonadotropin Releasing Factor (Gnrf) - Diphtheria Toxoid Conjugate 1
Hyaluronate Sodium 1
Sotalol 1
Tramadol 1
O 1
Deracoxib 1
Sulfa 1
Altrenogest Oily Solution 1
Anti-Il31 Mab Mcs Lot #1283563 1
Lufenuron + Milbemycin Oxime 1
Melarsomine Dihydrochloride 1
Fluralaner/Moxidectin Spot-On 1
Estriol Tablets 1
Desoxycortone Pivalate 1
Fluoxetine 1
Frunevetmab 1

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 Endocrine system disorder NOS (#2206 of 2,481 by report volume); death-coded 11.1%. PlainBreed reaction plate · report volume stamp 18 · 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 →