Drug profile

The FDA adverse-event record for Distemper-Adenovirus-Parvo-Pi

36 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Distemper-Adenovirus-Parvo-Pi. See the species affected, top reactions, and outcomes below.

36
adverse-event reports
11.1%
death-coded share
Dog
most-reported species
17
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.
36
Total Reports
4
Deaths Reported
11.1%
Death Rate

Active Ingredients

Distemper-Adenovirus-Parvo-Pi

Administration Routes

SubcutaneousUnknown

Species Affected

Dog 36

Most Affected Breeds

Chihuahua 5
Boxer (German Boxer) 3
Dachshund (unspecified) 3
Terrier - Bull - American Pit 3
Retriever - Labrador 3
Shih Tzu 2
Maltese 2
Shepherd Dog - German 1
Terrier (unspecified) 1
Shepherd Dog - Australian 1

Most Reported Reactions

Vomiting 17
Facial swelling (see also 'Skin') 12
Hives (see also 'Skin') 9
Lethargy (see also Central nervous system depression in 'Neurological') 8
Anaphylaxis 7
Diarrhoea 5
Death 4
Pale mucous membrane 4
Allergic reaction 3
Laboured breathing 2
Lateral recumbency 2
Hypothermia 2

Outcome Breakdown

Recovered/Normal
16 (44.4%)
Ongoing
14 (38.9%)
Died
4 (11.1%)
Outcome Unknown
2 (5.6%)

Distemper-Adenovirus-Parvo-Pi Adverse Event Insights

36 reports name Distemper-Adenovirus-Parvo-Pi; 4 recorded a death outcome (11.1% of reported events, not a population-level mortality rate). Active ingredient: Distemper-Adenovirus-Parvo-Pi. Administration routes: Subcutaneous, Unknown.

By species: Dog (36 reports). By breed: Chihuahua (5), Boxer (German Boxer) (3), Dachshund (unspecified) (3).

Leading clinical signs: Vomiting (17), Facial swelling (see also 'Skin') (12), Hives (see also 'Skin') (9), Lethargy (see also Central nervous system depression in 'Neurological') (8). Outcome, 36 coded reports: Recovered/Normal leads at 44.4%.

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.