Clostridium Chauvoei + Clostridium Haemolyticum + Clostridium Novyi + Clostridium Perfringens Type C + Clostridium Perfringens Type D Bacterin Toxoid + Clostridium Septicum + Clostridium Sordellii
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
3
Deaths Reported
3000.0%
Death Rate
Active Ingredients
Clostridium ChauvoeiClostridium HaemolyticumClostridium NovyiClostridium Perfringens Type CClostridium Perfringens Type D Bacterin ToxoidClostridium SepticumClostridium Sordellii
Administration Routes
UnknownSubcutaneous
Species Affected
Cattle 10
Most Affected Breeds
Cattle (other) 10
Most Reported Reactions
Lack of efficacy - NOS 3
Death 2
Rectal prolapse 2
Anaphylaxis 1
INEFFECTIVE, PARASITE(S) 1
Pink eye 1
INEFFECTIVE, KCS 1
Lameness 1
Pneumonia 1
Skin abscess 1
Laceration 1
Unrelated death 1
Outcome Breakdown
Recovered/Normal
4 (36.4%)
Died
3 (27.3%)
Ongoing
2 (18.2%)
Outcome Unknown
2 (18.2%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.