Bovine Respiratory Syncytial Virus, Brsv375, Mlv; Bovine Viral Diarrhea Virus, 5

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33 adverse event reports submitted to the FDA

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
33
Total Reports
27
Deaths Reported
8180.0%
Death Rate

Active Ingredients

Bovine Respiratory Syncytial Virus, Brsv375, Mlv; Bovine Viral Diarrhea Virus, 5

Administration Routes

SubcutaneousUnknownIntramuscular

Species Affected

Cattle 29
Unknown 4

Most Affected Breeds

Cattle (other) 21
Unknown 4
Crossbred Bovine/Cattle 4
Cattle (unknown) 2
Aberdeen Angus 2

Most Reported Reactions

Lack of efficacy (bacteria) - NOS 28
Death 20
Lack of efficacy - NOS 4
PR-LUNG(S), LESION(S) 3
CULTURE/TITER DATA ABNORMAL 3
Missing Cap 3
DEATH-TREATMENT FAILURE 2
Underfilling, Container 2
Pneumonia 1
Lack of efficacy (protozoa) - Coccidia 1
Caps, Abnormal 1
Vials, Leaking 1

Outcome Breakdown

Died
27 (45.8%)
Outcome Unknown
14 (23.7%)
Recovered/Normal
10 (16.9%)
Ongoing
7 (11.9%)
Euthanized
1 (1.7%)

Data Summary

Metric Value
Total adverse event reports 33
Reports involving death 27
Case-fatality rate (reported events) 8180.0%
Distinct species in reports 2
Distinct breeds in reports 5
Distinct reactions reported 19
Active ingredients on file 1

Source: FDA Center for Veterinary Medicine — Adverse Event Reporting (CVM AER). Counts reflect voluntary reports only.

Bovine Respiratory Syncytial Virus, Brsv375, Mlv; Bovine Viral Diarrhea Virus, 5 Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 33 adverse event reports referencing Bovine Respiratory Syncytial Virus, Brsv375, Mlv; Bovine Viral Diarrhea Virus, 5, including 27 reports in which the animal died — a 8180.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Bovine Respiratory Syncytial Virus, Brsv375, Mlv; Bovine Viral Diarrhea Virus, 5. Reported administration routes include Subcutaneous, Unknown, Intramuscular. These numbers reflect voluntary submissions from pet owners, veterinarians, and manufacturers and therefore under-represent mild events and over-represent severe ones — a pattern the FDA has documented repeatedly for pharmacovigilance datasets.

The species most frequently named in Bovine Respiratory Syncytial Virus, Brsv375, Mlv; Bovine Viral Diarrhea Virus, 5 reports are Cattle (29 reports), Unknown (4 reports), with Cattle accounting for the largest share. Within those species, Cattle (other) (21), Unknown (4), Crossbred Bovine/Cattle (4) appear most often — though breed popularity and ownership density shape these counts as much as any drug-specific sensitivity. This distribution matters because the same active ingredient can behave very differently across body sizes, ages, and species physiology.

The most commonly reported clinical signs associated with Bovine Respiratory Syncytial Virus, Brsv375, Mlv; Bovine Viral Diarrhea Virus, 5 are Lack of efficacy (bacteria) - NOS (28), Death (20), Lack of efficacy - NOS (4), PR-LUNG(S), LESION(S) (3). Of the 59 reports with a coded outcome, Died is the leading category at 45.8%. Because FDA adverse event data describes correlation rather than causation, these figures are best used to frame informed questions with a veterinarian and to compare reporting patterns across related products — not as a standalone safety verdict on Bovine Respiratory Syncytial Virus, Brsv375, Mlv; Bovine Viral Diarrhea Virus, 5.

Source: FDA Center for Veterinary Medicine — Adverse Event Reports FDA Center for Veterinary Medicine — Adverse Event Reports Data reflects voluntary submissions and may not represent actual incidence rates

Related

Data sourced from official AKC, AVMA, ACVO, and breed-club veterinary references. See our methodology for details. Retrieved and formatted by PlainBreed Editorial