Drug profile

The FDA adverse-event record for Lubabegron Fumarate

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

14
adverse-event reports
85.7%
death-coded share
Cattle
most-reported species
11
Death - 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.
14
Total Reports
12
Deaths Reported
85.7%
Death Rate

Active Ingredients

Lubabegron Fumarate

Administration Routes

OralUnknown

Species Affected

Cattle 13
Unknown 1

Most Affected Breeds

Mixed (Cattle) 9
Cattle (unknown) 2
Unknown 1
Charolais 1
Aberdeen Angus 1

Most Reported Reactions

Death 11
Unclassifiable adverse event 9
Necropsy performed 3
Acute (interstitial) pneumonia/pleuropneumonia 2
Contamination, Foreign Object 1
Found dead 1
Heavy breathing 1
Downer animal 1
Fibrinous (broncho) pneumonia/fibrinous pleuropneumonia 1
Pulmonary emphysema 1
Other abnormal test result NOS 1
Suppurative (broncho) pneumonia/pleuropneumonia 1

Outcome Breakdown

Died
12 (54.5%)
Outcome Unknown
10 (45.5%)

Lubabegron Fumarate Adverse Event Insights

14 reports name Lubabegron Fumarate; 12 recorded a death outcome (85.7% of reported events, not a population-level mortality rate). Active ingredient: Lubabegron Fumarate. Administration routes: Oral, Unknown.

By species: Cattle (13 reports), Unknown (1 reports). By breed: Mixed (Cattle) (9), Cattle (unknown) (2), Unknown (1).

Leading clinical signs: Death (11), Unclassifiable adverse event (9), Necropsy performed (3), Acute (interstitial) pneumonia/pleuropneumonia (2). Outcome, 22 coded reports: Died leads at 54.5%.

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.