Drug profile

The FDA adverse-event record for Other/Non-Product

22 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Other/Non-Product. See the species affected, top reactions, and outcomes below.

22
adverse-event reports
13.6%
death-coded share
Unknown
most-reported species
6
Containers, Leaking - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
22
Total Reports
3
Deaths Reported
13.6%
Death Rate

Active Ingredients

Other/Non-Product

Administration Routes

UnknownParenteralIntravenousOtherAuricular (Otic)

Species Affected

Unknown 13
Dog 3
Cattle 3
Human 2
Cat 1

Most Affected Breeds

Unknown 15
Cattle (other) 3
Beagle 2
Domestic Shorthair 1
Shepherd Dog - German 1

Most Reported Reactions

Containers, Leaking 6
Administration device NOS, priming issue 4
Necropsy performed 3
Lung oedema 3
Bronchopneumonia 3
Found dead 3
Accidental exposure 2
Administration device NOS, abnormal 2
Adaptor, abnormal 2
Administration device NOS, leaking 2
Digestive tract disorder NOS 2
Lack of efficacy (endoparasite) - tapeworm 2

Outcome Breakdown

Outcome Unknown
4 (44.4%)
Died
3 (33.3%)
Recovered/Normal
2 (22.2%)

Other/Non-Product Adverse Event Insights

22 reports name Other/Non-Product; 3 recorded a death outcome (13.6% of reported events, not a population-level mortality rate). Active ingredient: Other/Non-Product. Administration routes: Unknown, Parenteral, Intravenous, Other.

By species: Unknown (13 reports), Dog (3 reports), Cattle (3 reports). By breed: Unknown (15), Cattle (other) (3), Beagle (2).

Leading clinical signs: Containers, Leaking (6), Administration device NOS, priming issue (4), Necropsy performed (3), Lung oedema (3). Outcome, 9 coded reports: Outcome Unknown leads at 44.4%.

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.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.