Reaction profile

The FDA adverse-event record for hypovolaemic shock

54 FDA reports name hypovolaemic shock, a lower-volume reaction in the CVM extract (VeDDRA 2675). Plate stamps and neighbourhood peers follow.

#1699 of 2,481
by report volume (all reactions)
54
reports citing this reaction
51.9%
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. Hypovolaemic shock has 54 reports now versus 49 in that prior snapshot: 5 more (10.2%).

Report change
+5
Death-coded reports
+2
Death-coded share
−1.2 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 Hypovolaemic shock changes

FDA AER · VeDDRA plate

Code 2675 VOL-LOW

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

  • VOL-LOW 54 reports
  • DEATH-HOT 51.9%
  • MID-PACK #1699/2481
  • PHOTO-FINISH Acute mastitis
  • SPECIES-DOG Dog · 44
  • DRUG-LEAD Bedinvetmab · 10
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Acute mastitis (±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 Hypovolaemic shock

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

Vomiting · highest174348Acute mastitis · near54Arthropathy NOS · near54Exophthalmia · near54Hypovolaemic shock · this re…54INEFFECTIVE, COGNITIV… · near54Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Hypovolaemic shock

Hypovolaemic shock: high death-coded share in the FDA AER plate

Signature read: Hypovolaemic shock's 51.9% death-coded share is among the highest in the openFDA reaction corpus. Report volume is lower-third scale: 54 named reports in the openFDA extract. Death-coded share is upper-third: 28 of 54 reports (51.9% of named reports). Nearest volume peer: Acute mastitis (±0 reports). Lead species Dog (44). Lead co-reported drug Bedinvetmab (10).

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

Dog 44
Cat 10

Breeds Most Affected

Retriever - Labrador 11
Domestic Shorthair 7
Terrier - Bull - American Pit 4
Shepherd Dog - German 4
Shih Tzu 2
Pit Bull 2
Crossbred Canine/dog 2
Bulldog - English 2
Norwegian Forest 1
Shepherd Dog - Australian 1

Associated Drugs

Bedinvetmab 10
Gabapentin 9
Carprofen 6
Moxidectin 6
Buprenorphine 5
Maropitant Citrate 5
Polysulfated Glycosaminoglycan 5
Oclacitinib Maleate 5
Butorphanol 4
Melarsomine Dihydrochloride 4
Rabies Vaccine 4
Afoxolaner 4
Isoflurane 4
Galliprant 4
Pantoprazole 3
Prednisone 3
Deracoxib 3
Diphenhydramine 3
Oxygen 3
Enrofloxacin 3

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Hypovolaemic shock, 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 (54 here).

Similar death-coded share

Nearest other reactions by death-coded share (51.9% 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 Hypovolaemic shock (#1699 of 2,481 by report volume); death-coded 51.9%. PlainBreed reaction plate · death-coded share stamp 51.9% · 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 →