Drug profile

The FDA adverse-event record for Bovine Corona Des Lv

24 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Bovine Corona Des Lv. See the species affected, top reactions, and outcomes below.

24
adverse-event reports
62.5%
death-coded share
Cattle
most-reported species
12
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.
24
Total Reports
15
Deaths Reported
62.5%
Death Rate

Active Ingredients

Bovine Corona Des Lv

Administration Routes

NasalUnknownSubcutaneous

Species Affected

Cattle 24

Most Affected Breeds

Cattle (other) 12
Aberdeen Angus 4
Holstein-Friesian also known as Holstein 3
Crossbred Bovine/Cattle 3
Hereford cattle 2

Most Reported Reactions

Death 12
Lack of efficacy - NOS 11
Lack of efficacy (bacteria) - NOS 7
Lack of efficacy (virus) - coronavirus - NOS 5
Lack of efficacy (mycoplasma) - NOS 3
INEFFECTIVE, ANTIBIOTIC 2
NT - suppurative (broncho) pneumonia/pleuropneumonia 1
Vasculitis 1
Thrombosis 1
Tracheitis 1
Tracheal and laryngeal disorder NOS 1
Found dead 1

Outcome Breakdown

Ongoing
18 (35.3%)
Died
14 (27.5%)
Recovered/Normal
13 (25.5%)
Outcome Unknown
4 (7.8%)
Euthanized
2 (3.9%)

Bovine Corona Des Lv Adverse Event Insights

24 reports name Bovine Corona Des Lv; 15 recorded a death outcome (62.5% of reported events, not a population-level mortality rate). Active ingredient: Bovine Corona Des Lv. Administration routes: Nasal, Unknown, Subcutaneous.

By species: Cattle (24 reports). By breed: Cattle (other) (12), Aberdeen Angus (4), Holstein-Friesian also known as Holstein (3).

Leading clinical signs: Death (12), Lack of efficacy - NOS (11), Lack of efficacy (bacteria) - NOS (7), Lack of efficacy (virus) - coronavirus - NOS (5). Outcome, 51 coded reports: Ongoing leads at 35.3%.

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.