Reaction profile

The FDA adverse-event record for urinary retention

414 FDA reports name urinary retention, a high-volume reaction in the CVM extract (VeDDRA 737). Plate stamps and neighbourhood peers follow.

#712 of 2,481
by report volume (all reactions)
414
reports citing this reaction
17.4%
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. Urinary retention has 414 reports now versus 401 in that prior snapshot: 13 more (3.2%).

Report change
+13
Death-coded reports
+0
Death-coded share
−0.6 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 Urinary retention changes

FDA AER · VeDDRA plate

Code 737 VOL-LOW

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

  • VOL-LOW 414 reports
  • DEATH-ELEV 17.4%
  • MID-PACK #712/2481
  • PHOTO-FINISH Allergic dermatitis
  • SPECIES-DOG Dog · 290
  • DRUG-LEAD Buprenorphine · 65
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Allergic dermatitis (±0 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 Urinary retention

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

Vomiting · highest174348Scooting · near415Allergic dermatitis · near414Incorrect storage of… · near414Urinary retention · this rea…414Spasm · near413Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Urinary retention

What the FDA AER plate says about Urinary retention

Signature read: 72 death-coded reports is a heavy tail count for Urinary retention in the CVM extract. Report volume is upper-third scale: 414 named reports in the openFDA extract. 72 of 414 reports were death-coded (17.4% of named reports, not a population mortality rate). Nearest volume peer: Allergic dermatitis (±0 reports). Lead species Dog (290). Lead co-reported drug Buprenorphine (65).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Buprenorphine 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 290
Cat 119
Horse 4
Ferret 1

Breeds Most Affected

Domestic Shorthair 58
Retriever - Labrador 33
Crossbred Canine/dog 18
Cat (unknown) 17
Retriever - Golden 16
Shepherd Dog - German 15
Chihuahua 12
Dog (unknown) 12
Terrier - Yorkshire 11
Boxer (German Boxer) 9

Associated Drugs

Buprenorphine 65
Carprofen 46
Milbemycin Oxime + Spinosad 45
Bedinvetmab 43
Maropitant Citrate 36
Gabapentin 28
Isoflurane 27
Fentanyl 21
Spinosad 19
Ketamine 19
Propofol 17
Butorphanol 17
Oclacitinib Maleate 16
Robenacoxib 16
Dexmedetomidine 15
Nitenpyram 14
Cefovecin 14
Phenylpropanolamine Hcl 13
Melarsomine Dihydrochloride 12
Tramadol 12

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Urinary retention, 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 (414 here).

Similar death-coded share

Nearest other reactions by death-coded share (17.4% 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 Urinary retention (#712 of 2,481 by report volume); death-coded 17.4%. PlainBreed reaction plate · death-coded report count stamp 72 · 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 →