Drug profile

The FDA adverse-event record for Proin

232 FDA reports name Proin, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#502 of 2,679
by report volume (all drugs)
232
adverse-event reports
15.1%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Proin ranks #501 of 2679 by total reports (232) and #360 of 1130 by death-coded share (15.1%). National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#501
This drug, reports of 2679
#360
This drug, death share of 1130

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

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. Proin has 232 reports now versus 230 in that prior snapshot: 2 more (0.9%).

Report change
+2
Death-coded reports
+0
Death-coded share
−0.1 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 Proin changes

Signature read: death-coded report count at 35 is the most distinctive stamp on Proin's FDA AER row.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
232
Total Reports
35
Deaths Reported
15.1%
Death-coded share of reports

Active Ingredients

Proin

Administration Routes

UnknownOralTopical

Species Affected

Dog 230
Cat 2

Most Affected Breeds

Retriever - Labrador 44
Shepherd Dog - German 15
Crossbred Canine/dog 14
Shepherd Dog - Australian 11
Collie - Border 8
Doberman Pinscher 8
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 8
Siberian Husky 7
Deutsche Dogge, Great Dane 7
Spaniel (unspecified) 5

Most Reported Reactions

Vomiting 33
Urinary incontinence 32
Polydipsia 31
Death by euthanasia 27
Lethargy (see also Central nervous system depression in Neurological) 27
Polyuria 26
Ataxia 23
Not eating 22
Diarrhoea 20
Seizure NOS 19
Decreased appetite 18
Panting 14

Outcome Breakdown

Ongoing
134 (57.8%)
Recovered/Normal
42 (18.1%)
Euthanized
27 (11.6%)
Outcome Unknown
20 (8.6%)
Died
8 (3.4%)
Recovered with Sequela
1 (0.4%)

Proin: high report volume in the FDA AER row

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

High-volume nationwide drug peers

Two openFDA-derived peer sets for Proin, both floored at ≥50 reports so the neighborhoods stay in the advertised mass.

Similar death-coded share

Nearest other drugs by death-coded share (15.1% here), distinct from the volume row.

What to do with this drug

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 Proin (#502 of 2,679 by report volume); death-coded 15.1%. PlainBreed drug row · death-coded report count stamp 35 · 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 →