Clostridium Chauvoei Bacterin Toxoid + Clostridium Novyi Bacterin Toxoid + Clostridium Perfringens Type C Bacterin Toxoid + Clostridium Perfringens Type D Bacterin Toxoid + Clostridium Septicum Bacterin Toxoid + Clostridium Sordellii Bacterin Toxoid
34 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.
34
Total Reports
29
Deaths Reported
8530.0%
Death Rate
Active Ingredients
Clostridium Chauvoei Bacterin ToxoidClostridium Novyi Bacterin ToxoidClostridium Perfringens Type C Bacterin ToxoidClostridium Perfringens Type D Bacterin ToxoidClostridium Septicum Bacterin ToxoidClostridium Sordellii Bacterin Toxoid
Administration Routes
UnknownSubcutaneousIntramuscular
Species Affected
Cattle 34
Most Affected Breeds
Cattle (other) 19
Crossbred Bovine/Cattle 6
Cattle (unknown) 4
Aberdeen Angus 3
Charolais 1
Holstein-Friesian also known as Holstein 1
Most Reported Reactions
Death 26
Lack of efficacy - NOS 22
Depression 3
Anorexia 3
Necropsy performed 3
Bloody diarrhoea 2
Fever 2
Death by euthanasia 2
Lack of efficacy (bacteria) - NOS 2
Recumbency 1
NT - necrohemorrhagic enteritis 1
NT - ulcerative colitis 1
Outcome Breakdown
Died
28 (50.0%)
Outcome Unknown
12 (21.4%)
Recovered/Normal
7 (12.5%)
Ongoing
6 (10.7%)
Recovered with Sequela
2 (3.6%)
Euthanized
1 (1.8%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.