Reaction profile

The FDA adverse-event record for nt - hypertrophic dilated cardiomyopathy

18 FDA reports name nt - hypertrophic dilated cardiomyopathy, a lower-volume reaction in the CVM extract (VeDDRA 2302). Plate stamps and neighbourhood peers follow.

#2220 of 2,481
by report volume (all reactions)
18
reports citing this reaction
77.8%
death-coded share
Cat
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. NT - hypertrophic dilated cardiomyopathy has 18 reports now versus 17 in that prior snapshot: 1 more (5.9%).

Report change
+1
Death-coded reports
+0
Death-coded share
−4.6 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 NT - hypertrophic dilated cardiomyopathy changes

FDA AER · VeDDRA plate

Code 2302 VOL-TRACE

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

  • VOL-TRACE 18 reports
  • DEATH-HOT 77.8%
  • LOWER-Q #2220/2481
  • PHOTO-FINISH ALBUMIN/GLOBULIN RATI…
  • SPECIES-CAT Cat · 11
  • DRUG-LEAD Fluralaner Spot-O… · 2
  • DESK-WIDE 11 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: ALBUMIN/GLOBULIN RATIO HI, BLD (±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.

Lower-volume neighbourhood around NT - hypertrophic dilated cardiomyopathy

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 · near18NT - hypertrophic dil… · thi…18Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around NT - hypertrophic dilated cardiomyopathy

NT - hypertrophic dilated cardiomyopathy: high death-coded share in the FDA AER plate

Signature read: NT - hypertrophic dilated cardiomyopathy's 77.8% death-coded share is among the highest in the openFDA reaction corpus. Report volume is lower-third scale: 18 named reports in the openFDA extract. Death-coded share is upper-third: 14 of 18 reports (77.8% of named reports). Nearest volume peer: ALBUMIN/GLOBULIN RATIO HI, BLD (±0 reports). Lead species Cat (11). Lead co-reported drug Fluralaner Spot-On Solution (2).

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

Cat 11
Dog 6
Chicken 1

Breeds Most Affected

Domestic Shorthair 7
Domestic Longhair 2
Tosa 1
Boxer (German Boxer) 1
Pit Bull 1
Alaskan Malamute 1
Rottweiler 1
Cat (other) 1
Chicken (other) 1
Mountain Dog - Bernese 1

Associated Drugs

Fluralaner Spot-On Solution 2
Cefovecin 2
Fluralaner/Moxidectin Spot-On 2
Spinosad 1
Rabies Vaccine 1
Trilostane 1
Fluralaner Chew Tablets 1
Genta/Momet/Clotrim Ear Oint 1
Acepromazine Maleate 1
Rabies Vaccine, Killed Virus 1
Feline Rhinotracheitis Calici Panleukopenia Vaccine, Killed Virus 1
Insulin Injectable Vial 1
Melarsomine Dihydrochloride Injection 1
Itraconazole 1
Gentamicin Sulfate + Betamethasone Valerate 1
Grapiprant 1
Enrofloxacin 1
Finasteride 1
Nitenpyram 1
Rabies In Hhh Adj Pfizer Kv 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 NT - hypertrophic dilated cardiomyopathy (#2220 of 2,481 by report volume); death-coded 77.8%. PlainBreed reaction plate · death-coded share stamp 77.8% · 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 →