Reaction profile

The FDA adverse-event record for hyposthenuria

523 FDA reports name hyposthenuria, a high-volume reaction in the CVM extract (VeDDRA 2475). Plate stamps and neighbourhood peers follow.

#631 of 2,481
by report volume (all reactions)
523
reports citing this reaction
8.4%
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. Hyposthenuria has 523 reports now versus 501 in that prior snapshot: 22 more (4.4%).

Report change
+22
Death-coded reports
+0
Death-coded share
−0.4 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 Hyposthenuria changes

FDA AER · VeDDRA plate

Code 2475 VOL-MID

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

  • VOL-MID 523 reports
  • DEATH-PAR 8.4%
  • MID-PACK #631/2481
  • PHOTO-FINISH Collapse of leg
  • SPECIES-DOG Dog · 485
  • DRUG-LEAD Bedinvetmab · 199
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Collapse of leg (±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 Hyposthenuria

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

Vomiting · highest174348Collapse of leg · near524INEFFECTIVE, ANTIEMET… · near524Hyposthenuria · this reaction523Hypocortisolaemia · near521Papilloma · near521Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Hyposthenuria

What the FDA AER plate says about Hyposthenuria

Signature read: 523 reports place Hyposthenuria in the upper third of FDA AER volume (#631 of 2,481). Report volume is upper-third scale: 523 named reports in the openFDA extract. 44 of 523 reports were death-coded (8.4% of named reports, not a population mortality rate). Nearest volume peer: Collapse of leg (±1 reports). Lead species Dog (485). Lead co-reported drug Bedinvetmab (199).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Bedinvetmab 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 485
Cat 33
Horse 5

Breeds Most Affected

Retriever - Labrador 81
Crossbred Canine/dog 34
Shepherd Dog - German 21
Retriever - Golden 21
Domestic Shorthair 21
Shepherd Dog - Australian 18
Boxer (German Boxer) 17
Chihuahua 11
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 11
Beagle 10

Associated Drugs

Bedinvetmab 199
Trilostane 131
Gabapentin 60
Carprofen 47
Oclacitinib Maleate 45
Maropitant Citrate 43
Anti-Il31 Mab Mcs Lot #1283563 22
Pyrantel Pamoate;Sarolaner 19
Fluralaner 13.64% 12-Week Chew 17
Fluralaner Chew Tablets 16
Prednisone 16
Grapiprant 15
Tramadol 13
Metronidazole 12
Cefovecin 11
Moxidectin 11
Doxycycline 11
Desoxycorticosterone Pivalate 9
Firocoxib 9
Enrofloxacin 9

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Hyposthenuria, 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 (523 here).

Similar death-coded share

Nearest other reactions by death-coded share (8.4% 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 Hyposthenuria (#631 of 2,481 by report volume); death-coded 8.4%. PlainBreed reaction plate · report volume stamp 523 · 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 →