Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D Bacterin-Toxoid

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10 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.
10
Total Reports
9
Deaths Reported
9000.0%
Death Rate

Active Ingredients

Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D Bacterin-Toxoid

Administration Routes

SubcutaneousUnknownSubconjunctival

Species Affected

Cattle 10

Most Affected Breeds

Cattle (unknown) 2
Cattle (other) 2
Crossbred Bovine/Cattle 2
Unknown 1
Aberdeen Angus 1
Holstein-Friesian also known as Holstein 1
Senepol 1

Most Reported Reactions

Death 7
Recumbency 2
Death by euthanasia 2
Fever 2
Other abnormal test result NOS 2
Lack of efficacy - NOS 2
CULTURE/TITER DATA ABNORMAL 2
Injection site abscess 2
Staggering 1
Foaming at the mouth 1
Sudden death 1
Cardiac enlargement 1

Outcome Breakdown

Died
8 (53.3%)
Recovered/Normal
3 (20.0%)
Euthanized
2 (13.3%)
Ongoing
1 (6.7%)
Outcome Unknown
1 (6.7%)

Data Summary

Metric Value
Total adverse event reports 10
Reports involving death 9
Case-fatality rate (reported events) 9000.0%
Distinct species in reports 1
Distinct breeds in reports 7
Distinct reactions reported 20
Active ingredients on file 1

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

Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D Bacterin-Toxoid Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 10 adverse event reports referencing Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D Bacterin-Toxoid, including 9 reports in which the animal died — a 9000.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D Bacterin-Toxoid. Reported administration routes include Subcutaneous, Unknown, Subconjunctival. 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 Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D Bacterin-Toxoid reports are Cattle (10 reports), with Cattle accounting for the largest share. Within those species, Cattle (unknown) (2), Cattle (other) (2), Crossbred Bovine/Cattle (2) 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 Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D Bacterin-Toxoid are Death (7), Recumbency (2), Death by euthanasia (2), Fever (2). Of the 15 reports with a coded outcome, Died is the leading category at 53.3%. 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 Clostridium Chauvoei-Septicum-Novyi-Sordellii-Perfringens Types C And D Bacterin-Toxoid.

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