Drug profile

The FDA adverse-event record for Rabies Virus,Pv-11,Killed

462 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Rabies Virus,Pv-11,Killed. See the species affected, top reactions, and outcomes below.

462
adverse-event reports
10.2%
death-coded share
Dog
most-reported species
147
Vomiting - 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.
462
Total Reports
47
Deaths Reported
10.2%
Death Rate

Active Ingredients

Rabies Virus,Pv-11,Killed

Administration Routes

SubcutaneousUnknownIntramuscularNasalOral

Species Affected

Dog 397
Cat 39
Horse 25
Mule 1

Most Affected Breeds

Chihuahua 45
Retriever - Labrador 33
Domestic Shorthair 25
Retriever - Golden 23
Terrier - Yorkshire 16
Shih Tzu 15
Dachshund (unspecified) 14
Quarter Horse 12
Maltese 12
Pit Bull 11

Most Reported Reactions

Vomiting 147
Lethargy (see also Central nervous system depression in 'Neurological') 83
Diarrhoea 70
Anorexia 38
Injection site lump 37
Neutrophilia 32
Other abnormal test result NOS 32
Lethargy (see also Central nervous system depression in Neurological) 32
Seizure NOS 30
Fever 30
Death 27
Not eating 26

Outcome Breakdown

Outcome Unknown
195 (42.1%)
Recovered/Normal
165 (35.6%)
Ongoing
54 (11.7%)
Died
29 (6.3%)
Euthanized
19 (4.1%)
Recovered with Sequela
1 (0.2%)

Rabies Virus,Pv-11,Killed Adverse Event Insights

462 reports name Rabies Virus,Pv-11,Killed; 47 recorded a death outcome (10.2% of reported events, not a population-level mortality rate). Active ingredient: Rabies Virus,Pv-11,Killed. Administration routes: Subcutaneous, Unknown, Intramuscular, Nasal.

By species: Dog (397 reports), Cat (39 reports), Horse (25 reports). By breed: Chihuahua (45), Retriever - Labrador (33), Domestic Shorthair (25).

Leading clinical signs: Vomiting (147), Lethargy (see also Central nervous system depression in 'Neurological') (83), Diarrhoea (70), Anorexia (38). Outcome, 463 coded reports: Outcome Unknown leads at 42.1%.

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.