Unspecified Nsaid

21 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.
21
Total Reports
3
Deaths Reported
1430.0%
Death Rate

Active Ingredients

Unspecified Nsaid

Administration Routes

UnknownOral

Species Affected

Dog 18
Horse 2
Cat 1

Most Affected Breeds

Retriever - Labrador 3
Beagle 2
Shepherd Dog - German 2
Dachshund - Miniature 1
Corgi - Welsh Cardigan 1
Shih Tzu 1
Horse (unknown) 1
Friesian 1
Pointer (unspecified) 1
Dog (other) 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in Neurological) 6
Diarrhoea 4
Lethargy (see also Central nervous system depression in 'Neurological') 4
Anorexia 4
Hind limb paresis 3
Vomiting 3
Death by euthanasia 3
Reluctant to move 2
Panting 2
General illness 2
Skin lesion NOS 2
Localised hair loss 2

Outcome Breakdown

Outcome Unknown
8 (38.1%)
Ongoing
6 (28.6%)
Recovered/Normal
4 (19.0%)
Euthanized
3 (14.3%)

Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.