Drug profile

The FDA adverse-event record for Canine Parvovirus Mab

23 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Canine Parvovirus Mab. Species, reactions, and outcomes follow.

#1641 of 2,679
by report volume (all drugs)
23
adverse-event reports
56.5%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Canine Parvovirus Mab ranks #1638 of 2679 by total reports (23). Death-coded-share rank requires at least 50 reports. National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#1638
This drug, reports of 2679

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Canine Parvovirus Mab has 23 reports now versus 14 in that prior snapshot: 9 more (64.3%).

Report change
+9
Death-coded reports
+4
Death-coded share
−7.8 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Canine Parvovirus Mab changes

Signature read: Canine Parvovirus Mab's 56.5% death-coded share is among the highest in the openFDA drug corpus.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
23
Total Reports
13
Deaths Reported
56.5%
Death-coded share of reports

Active Ingredients

Canine Parvovirus Mab

Administration Routes

IntravenousUnknownParenteralSubcutaneous

Species Affected

Dog 23

Most Affected Breeds

Poodle (unspecified) 3
Retriever - Labrador 3
Dog (unknown) 2
Collie - Border 2
Shepherd Dog - German 2
Sheepdog - Shetland 1
Shepherd Dog - Belgian Malinois 1
Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog) 1
Coonhound - Bluetick 1
Pointing Dog - German Short-haired 1

Most Reported Reactions

Death 12
Lack of efficacy (virus) - parvovirus (including feline panleukopenia) 12
Diarrhoea 5
Lateral recumbency 4
Death by euthanasia 4
Unclassifiable adverse event 4
Vomiting 4
Lethargy (see also Central nervous system depression in Neurological) 3
Behavioural disorder NOS 3
Hypoglycaemia 3
Other abnormal test result NOS 3
Seizure NOS 3

Outcome Breakdown

Died
12 (37.5%)
Outcome Unknown
8 (25.0%)
Ongoing
5 (15.6%)
Euthanized
4 (12.5%)
Recovered/Normal
3 (9.4%)

Canine Parvovirus Mab: high death-coded share in the FDA AER row

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.

What to do with this drug

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

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

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Canine Parvovirus Mab (#1641 of 2,679 by report volume); death-coded 56.5%. PlainBreed drug row · death-coded share stamp 56.5% · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →