Clostridium Chauvoei + Clostridium Novyi + Clostridium Perfringens Type C + Clostridium Perfringens Type D Bacterin Toxoid + Clostridium Septicum + Clostridium Sordellii
31 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.
31
Total Reports
24
Deaths Reported
7740.0%
Death Rate
Active Ingredients
Clostridium ChauvoeiClostridium NovyiClostridium Perfringens Type CClostridium Perfringens Type D Bacterin ToxoidClostridium SepticumClostridium Sordellii
Administration Routes
UnknownSubcutaneous
Species Affected
Cattle 31
Most Affected Breeds
Cattle (other) 18
Aberdeen Angus 7
Cattle (unknown) 4
Charolais 2
Most Reported Reactions
Death 23
Lack of efficacy - NOS 11
Lack of efficacy (bacteria) - NOS 3
Respiratory signs 2
Other abnormal test result NOS 2
CULTURE/TITER DATA ABNORMAL 2
Necropsy performed 2
Death by euthanasia 2
Injection site granuloma 1
Injection site infection 1
NT - fibrinous (broncho) pneumonia/fibrinous pleuropneumonia 1
INEFFECTIVE, WORMS 1
Outcome Breakdown
Died
24 (51.1%)
Outcome Unknown
10 (21.3%)
Recovered/Normal
7 (14.9%)
Ongoing
4 (8.5%)
Recovered with Sequela
1 (2.1%)
Euthanized
1 (2.1%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.