Paroxetine

11 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.

Total Reports

Deaths Reported

0.0%

Death Rate

Active Ingredients

Paroxetine

Administration Routes

UnknownOral

Species Affected

Dog 6

Cat 3

Human 2

Most Affected Breeds

Domestic Shorthair 3

Unknown 2

Pit Bull 1

Dachshund - Standard Smooth-haired 1

Bulldog - English 1

Shepherd (unspecified) 1

Retriever - Labrador 1

Poodle - Toy 1

Most Reported Reactions

Vomiting 3

Anxiety 2

Decreased appetite 2

Chest tightness 1

Indigestion 1

Urticaria 1

Erythema (for urticaria see Immune SOC) 1

Skin irritation 1

Cataract 1

Periodontal disorder 1

Eye disorder NOS (for photophobia see 'neurological') 1

Sleepiness - systemic disorder 1

Outcome Breakdown

Outcome Unknown

5 (45.5%)

Recovered/Normal

4 (36.4%)

Ongoing

2 (18.2%)

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