Prednisolone Sodium Succinate
140 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.
140
Total Reports
24
Deaths Reported
1710.0%
Death Rate
Active Ingredients
Prednisolone Sodium Succinate
Administration Routes
UnknownIntravenousIntramuscularOralSubcutaneous
Species Affected
Unknown 101
Dog 30
Cat 5
Horse 4
Most Affected Breeds
Unknown 101
Retriever - Labrador 5
Domestic Shorthair 3
Domestic (unspecified) 2
Shih Tzu 2
Terrier - Jack Russell 2
Chihuahua 2
Boxer (German Boxer) 2
Bulldog - French 2
Thoroughbred 1
Most Reported Reactions
Vials, Abnormal 45
Vials, Damaged 25
Death 18
Solution, Abnormal 11
No sign 10
Product Defect, General 9
Anaemia NOS 8
Pale mucous membrane 8
Vomiting 7
Uncoded sign 7
Leucocytosis NOS 6
Other abnormal test result NOS 6
Outcome Breakdown
Died
18 (51.4%)
Euthanized
6 (17.1%)
Ongoing
6 (17.1%)
Recovered/Normal
4 (11.4%)
Recovered with Sequela
1 (2.9%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.