Drug profile

The FDA adverse-event record for Purevax Feline 3/Rabies - 16T9.R0

27 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Purevax Feline 3/Rabies - 16T9.R0. See the species affected, top reactions, and outcomes below.

27
adverse-event reports
18.5%
death-coded share
Cat
most-reported species
7
Lethargy (see also Central nervous system depression in Neurological) - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
27
Total Reports
5
Deaths Reported
18.5%
Death Rate

Active Ingredients

Purevax Feline 3/Rabies - 16T9.R0

Administration Routes

SubcutaneousUnknown

Species Affected

Cat 27

Most Affected Breeds

Domestic Shorthair 20
Domestic Longhair 3
Chartreuse 1
British cat 1
Ragdoll 1
Cat (unknown) 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in Neurological) 7
Not eating 5
Vomiting 5
Fever 5
Ataxia 4
Hyperglycaemia 4
Neutrophilia 4
Diarrhoea 3
Lethargy (see also Central nervous system depression in 'Neurological') 3
Anorexia 3
Behavioural disorder NOS 3
Monocytosis 3

Outcome Breakdown

Recovered/Normal
11 (40.7%)
Outcome Unknown
9 (33.3%)
Euthanized
3 (11.1%)
Died
2 (7.4%)
Ongoing
2 (7.4%)

Purevax Feline 3/Rabies - 16T9.R0 Adverse Event Insights

27 reports name Purevax Feline 3/Rabies - 16T9.R0; 5 recorded a death outcome (18.5% of reported events, not a population-level mortality rate). Active ingredient: Purevax Feline 3/Rabies - 16T9.R0. Administration routes: Subcutaneous, Unknown.

By species: Cat (27 reports). By breed: Domestic Shorthair (20), Domestic Longhair (3), Chartreuse (1).

Leading clinical signs: Lethargy (see also Central nervous system depression in Neurological) (7), Not eating (5), Vomiting (5), Fever (5). Outcome, 27 coded reports: Recovered/Normal leads at 40.7%.

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.