Drug profile

The FDA adverse-event record for Ibr/Brsv/Pi3/Bvd Lv+Vib/Lep*5

12 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Ibr/Brsv/Pi3/Bvd Lv+Vib/Lep*5. See the species affected, top reactions, and outcomes below.

12
adverse-event reports
66.7%
death-coded share
Cattle
most-reported species
6
Lack of efficacy - NOS - 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.
12
Total Reports
8
Deaths Reported
66.7%
Death Rate

Active Ingredients

Ibr/Brsv/Pi3/Bvd Lv+Vib/Lep*5

Administration Routes

SubcutaneousUnknown

Species Affected

Cattle 12

Most Affected Breeds

Aberdeen Angus 5
Cattle (other) 3
Red Angus 2
Brangus 1
Simmental 1

Most Reported Reactions

Lack of efficacy - NOS 6
Death 5
Abortion 4
Found dead 2
Selenium toxicity signs 2
NT - Abnormal necropsy finding NOS 2
Respiratory signs 1
Lack of efficacy (bacteria NOS) 1
Lack of efficacy (virus) - herpesvirus NOS 1
Stillbirth 1
Liver disorder NOS 1
Infectious disease NOS 1

Outcome Breakdown

Died
8 (47.1%)
Ongoing
4 (23.5%)
Outcome Unknown
3 (17.6%)
Recovered/Normal
2 (11.8%)

Ibr/Brsv/Pi3/Bvd Lv+Vib/Lep*5 Adverse Event Insights

12 reports name Ibr/Brsv/Pi3/Bvd Lv+Vib/Lep*5; 8 recorded a death outcome (66.7% of reported events, not a population-level mortality rate). Active ingredient: Ibr/Brsv/Pi3/Bvd Lv+Vib/Lep*5. Administration routes: Subcutaneous, Unknown.

By species: Cattle (12 reports). By breed: Aberdeen Angus (5), Cattle (other) (3), Red Angus (2).

Leading clinical signs: Lack of efficacy - NOS (6), Death (5), Abortion (4), Found dead (2). Outcome, 17 coded reports: Died leads at 47.1%.

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.