Reaction profile

The FDA adverse-event record for low thyroxine (t4)

653 FDA reports name low thyroxine (t4), a high-volume reaction in the CVM extract (VeDDRA 2670). Plate stamps and neighbourhood peers follow.

#537 of 2,481
by report volume (all reactions)
653
reports citing this reaction
18.4%
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. Low thyroxine (T4) has 653 reports now versus 621 in that prior snapshot: 32 more (5.2%).

Report change
+32
Death-coded reports
+8
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 Low thyroxine (T4) changes

FDA AER · VeDDRA plate

Code 2670 VOL-MID

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

  • VOL-MID 653 reports
  • DEATH-ELEV 18.4%
  • UPPER-Q #537/2481
  • PHOTO-FINISH Dull
  • SPECIES-DOG Dog · 583
  • DRUG-LEAD Trilostane · 176
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Dull (±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 Low thyroxine

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

Vomiting · highest174348Low thyroxine (T4) · this re…653Dull · near652Tongue disorder NOS · near649Liver failure · near648Patient instructions… · near647Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Low thyroxine (T4)

What the FDA AER plate says about Low thyroxine (T4)

Signature read: 120 death-coded reports is a heavy tail count for Low thyroxine (T4) in the CVM extract. Report volume is upper-third scale: 653 named reports in the openFDA extract. 120 of 653 reports were death-coded (18.4% of named reports, not a population mortality rate). Nearest volume peer: Dull (±1 reports). Lead species Dog (583). Lead co-reported drug Trilostane (176).

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 583
Cat 70

Breeds Most Affected

Retriever - Labrador 73
Domestic Shorthair 55
Crossbred Canine/dog 41
Retriever - Golden 39
Shepherd Dog - German 24
Chihuahua 17
Boxer (German Boxer) 17
Maltese 15
Shepherd Dog - Australian 15
Terrier (unspecified) 14

Associated Drugs

Trilostane 176
Bedinvetmab 83
Maropitant Citrate 55
Levothyroxine Sodium 53
Oclacitinib Maleate 53
Carprofen 52
Gabapentin 48
Prednisone 39
Afoxolaner 35
Thiamazole 32
Pyrantel Pamoate;Sarolaner 31
Milbemycin Oxime + Spinosad 30
Fluralaner 13.64% 12-Week Chew 26
Levothyroxine 25
Grapiprant 21
Anti-Il31 Mab Mcs Lot #1283563 20
Doxycycline 18
Ilunocitinib 18
Moxidectin 17
Metronidazole 17

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Low thyroxine (T4), 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 (653 here).

Similar death-coded share

Nearest other reactions by death-coded share (18.4% 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 Low thyroxine (T4) (#537 of 2,481 by report volume); death-coded 18.4%. PlainBreed reaction plate · death-coded report count stamp 120 · 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 →