Device: Monitoring
30 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.
30
Total Reports
0
Deaths Reported
0.0%
Death Rate
Active Ingredients
Device: Monitoring
Administration Routes
UnknownTopical
Species Affected
Unknown 28
Human 1
Dog 1
Most Affected Breeds
Unknown 29
Dog (unknown) 1
Most Reported Reactions
Device Defective NOS 13
Product Defect, General 12
Lack of efficacy, medical device 4
Missing component, medical device 3
Tongue ulceration 3
Laceration 3
Burn 1
Application site necrosis 1
Tongue disorder NOS 1
Application site swelling 1
Outcome Breakdown
Outcome Unknown
5 (83.3%)
Recovered/Normal
1 (16.7%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.