Drug profile

The FDA adverse-event record for Equipment

210 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Equipment. See the species affected, top reactions, and outcomes below.

210
adverse-event reports
0.5%
death-coded share
Unknown
most-reported species
83
Dispenser, Abnormal - 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.
210
Total Reports
1
Deaths Reported
0.5%
Death Rate

Active Ingredients

Equipment

Administration Routes

UnknownOral

Species Affected

Unknown 209
Cattle 1

Most Affected Breeds

Unknown 209
Cattle (other) 1

Most Reported Reactions

Dispenser, Abnormal 83
Product Defect, General 82
Administration device NOS, malfunction 40
Product problem 31
Administration device NOS, leaking 24
Administration device NOS, abnormal 19
Caps, Abnormal 14
Administration device NOS, missing component 8
Administration device NOS, breakage 8
Containers, Leaking 7
Difficulty of Use 5
Closure, Abnormal 3

Outcome Breakdown

Ongoing
1 (50.0%)
Died
1 (50.0%)

Equipment Adverse Event Insights

210 reports name Equipment; 1 recorded a death outcome (0.5% of reported events, not a population-level mortality rate). Active ingredient: Equipment. Administration routes: Unknown, Oral.

By species: Unknown (209 reports), Cattle (1 reports). By breed: Unknown (209), Cattle (other) (1).

Leading clinical signs: Dispenser, Abnormal (83), Product Defect, General (82), Administration device NOS, malfunction (40), Product problem (31). Outcome, 2 coded reports: Ongoing leads at 50.0%.

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.