Drug profile

The FDA adverse-event record for Rabies Vaccine From Another Manufacturer

25 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Rabies Vaccine From Another Manufacturer. See the species affected, top reactions, and outcomes below.

25
adverse-event reports
12.0%
death-coded share
Dog
most-reported species
12
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.
25
Total Reports
3
Deaths Reported
12.0%
Death Rate

Active Ingredients

Rabies Vaccine From Another Manufacturer

Administration Routes

Subcutaneous

Species Affected

Dog 20
Cat 5

Most Affected Breeds

Domestic Shorthair 3
Terrier - Bull - American Pit 3
Retriever - Golden 3
Terrier - Yorkshire 2
Siberian Husky 1
Crossbred Canine/dog 1
Havanese 1
Domestic Longhair 1
Newfoundland 1
Mountain Dog - Bernese 1

Most Reported Reactions

Lethargy (see also Central nervous system depression in Neurological) 12
Vomiting 8
Not eating 6
Diarrhoea 4
Pale mucous membrane 4
Anaphylaxis 4
Not himself/herself 3
Hypersensitivity reaction 3
Facial swelling (see also Skin) 3
Hives (see also Skin) 2
Fever 2
Low blood pressure 2

Outcome Breakdown

Ongoing
15 (60.0%)
Recovered/Normal
6 (24.0%)
Euthanized
2 (8.0%)
Died
1 (4.0%)
Outcome Unknown
1 (4.0%)

Rabies Vaccine From Another Manufacturer Adverse Event Insights

25 reports name Rabies Vaccine From Another Manufacturer; 3 recorded a death outcome (12.0% of reported events, not a population-level mortality rate). Active ingredient: Rabies Vaccine From Another Manufacturer. Administration route: Subcutaneous.

By species: Dog (20 reports), Cat (5 reports). By breed: Domestic Shorthair (3), Terrier - Bull - American Pit (3), Retriever - Golden (3).

Leading clinical signs: Lethargy (see also Central nervous system depression in Neurological) (12), Vomiting (8), Not eating (6), Diarrhoea (4). Outcome, 25 coded reports: Ongoing leads at 60.0%.

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.