Reaction profile

The FDA adverse-event record for stranguria

392 FDA reports name stranguria, a high-volume reaction in the CVM extract (VeDDRA 738). Plate stamps and neighbourhood peers follow.

#737 of 2,481
by report volume (all reactions)
392
reports citing this reaction
13.3%
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. Stranguria has 392 reports now versus 386 in that prior snapshot: 6 more (1.6%).

Report change
+6
Death-coded reports
+0
Death-coded share
−0.2 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 Stranguria changes

FDA AER · VeDDRA plate

Code 738 VOL-LOW

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

  • VOL-LOW 392 reports
  • DEATH-ELEV 13.3%
  • MID-PACK #737/2481
  • PHOTO-FINISH Basophilia
  • SPECIES-DOG Dog · 287
  • DRUG-LEAD Bedinvetmab · 49
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Basophilia (±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 Stranguria

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

Vomiting · highest174348Mast cell tumour · near394Stranguria · this reaction392Basophilia · near391Urination related to… · near391Fasciculation · near390Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Stranguria

What the FDA AER plate says about Stranguria

Signature read: 52 death-coded reports is a heavy tail count for Stranguria in the CVM extract. Report volume is upper-third scale: 392 named reports in the openFDA extract. 52 of 392 reports were death-coded (13.3% of named reports, not a population mortality rate). Nearest volume peer: Basophilia (±1 reports). Lead species Dog (287). Lead co-reported drug Bedinvetmab (49).

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 287
Cat 100
Horse 2
Human 1
Ferret 1
Donkey 1

Breeds Most Affected

Domestic Shorthair 59
Retriever - Labrador 35
Crossbred Canine/dog 26
Shepherd Dog - German 16
Domestic (unspecified) 14
Retriever - Golden 12
Boxer (German Boxer) 11
Chihuahua 10
Shepherd Dog - Australian 9
Terrier - Bull - American Pit 9

Associated Drugs

Bedinvetmab 49
Oclacitinib Maleate 41
Carprofen 32
Gabapentin 23
Milbemycin Oxime + Spinosad 19
Meloxicam 16
Robenacoxib 15
Afoxolaner 14
Prednisone 13
Trilostane 12
Cefovecin 12
Moxidectin 12
Maropitant Citrate 11
Frunevetmab 11
Spinosad 10
Cyclosporine A 9
Buprenorphine 9
Fluralaner Chew Tablets 9
Ivermectin + Pyrantel As Pamoate Salt 9
Pyrantel Pamoate;Sarolaner 9

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Stranguria, 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 (392 here).

Similar death-coded share

Nearest other reactions by death-coded share (13.3% 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 Stranguria (#737 of 2,481 by report volume); death-coded 13.3%. PlainBreed reaction plate · death-coded report count stamp 52 · 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 →