Flunixin Meglumine Oral Paste
58 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.
58
Total Reports
1
Deaths Reported
170.0%
Death Rate
Active Ingredients
Flunixin Meglumine Oral Paste
Administration Routes
OralUnknownTopical
Species Affected
Unknown 28
Horse 23
Dog 4
Human 2
Other Camelids 1
Most Affected Breeds
Unknown 31
Quarter Horse 3
Miniature 3
Warmblood (unspecified) 3
Paint 2
Crossbred Canine/dog 2
Hanovarian 2
Horse (unknown) 1
Shepherd Dog - German 1
Irish Hunter 1
Most Reported Reactions
Fever 9
Product problem 7
Appearance, Abnormal 5
Defect Unknown/Not Specified 5
Tubes, Abnormal 4
Vomiting 4
Pale mucous membrane 3
Tubes, Leaking 3
Containers, Leaking 3
Colic 3
Product syringe issue 3
Underfilling, Container 3
Outcome Breakdown
Ongoing
14 (46.7%)
Recovered/Normal
10 (33.3%)
Outcome Unknown
4 (13.3%)
Recovered with Sequela
1 (3.3%)
Died
1 (3.3%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.