Drug profile

The FDA adverse-event record for Lepto Vaccine

468 FDA reports name Lepto Vaccine, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#318 of 2,679
by report volume (all drugs)
468
adverse-event reports
9.4%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Lepto Vaccine ranks #318 of 2679 by total reports (468) and #571 of 1130 by death-coded share (9.4%). 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)
#318
This drug, reports of 2679
#571
This drug, death share of 1130

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. Lepto Vaccine has 468 reports now versus 462 in that prior snapshot: 6 more (1.3%).

Report change
+6
Death-coded reports
+0
Death-coded share
−0.1 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 Lepto Vaccine changes

Signature read: 468 reports place Lepto Vaccine in the upper third of FDA AER volume (#318 of 2,679).

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
468
Total Reports
44
Deaths Reported
9.4%
Death-coded share of reports

Active Ingredients

Lepto Vaccine

Administration Routes

UnknownParenteralSubcutaneousIntra-ArterialOral

Species Affected

Dog 468

Most Affected Breeds

Retriever - Labrador 65
Retriever - Golden 26
Shepherd Dog - German 24
Boxer (German Boxer) 23
Crossbred Canine/dog 20
Shih Tzu 20
Pit Bull 15
Shepherd Dog - Australian 13
Dachshund (unspecified) 12
Bulldog - French 12

Most Reported Reactions

Vomiting 148
Emesis 89
Lethargy (see also Central nervous system depression in 'Neurological') 81
Diarrhoea 72
Other abnormal test result NOS 36
Seizure NOS 32
Lack of efficacy - NOS 26
Decreased appetite 26
Death 23
Behavioural disorder NOS 23
Not eating 22
Shaking 20

Outcome Breakdown

Recovered/Normal
220 (47.0%)
Outcome Unknown
99 (21.2%)
Ongoing
84 (17.9%)
Died
25 (5.3%)
Recovered with Sequela
21 (4.5%)
Euthanized
19 (4.1%)

Lepto Vaccine: high report volume 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.

High-volume nationwide drug peers

Two openFDA-derived peer sets for Lepto Vaccine, both floored at ≥50 reports so the neighborhoods stay in the advertised mass.

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 Lepto Vaccine (#318 of 2,679 by report volume); death-coded 9.4%. PlainBreed drug row · report volume stamp 468 · 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 →