Drug profile

The FDA adverse-event record for Lyme

64 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Lyme. Species, reactions, and outcomes follow.

#978 of 2,679
by report volume (all drugs)
64
adverse-event reports
10.9%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Lyme ranks #976 of 2679 by total reports (64) and #504 of 1130 by death-coded share (10.9%). 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)
#976
This drug, reports of 2679
#504
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. Lyme has 64 reports now versus 59 in that prior snapshot: 5 more (8.5%).

Report change
+5
Death-coded reports
+2
Death-coded share
+2.5 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 Lyme changes

Signature read: report volume at 64 is the most distinctive stamp on Lyme's FDA AER row.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
64
Total Reports
7
Deaths Reported
10.9%
Death-coded share of reports

Active Ingredients

Lyme

Administration Routes

SubcutaneousUnknown

Species Affected

Dog 64

Most Affected Breeds

Crossbred Canine/dog 10
Retriever - Labrador 8
Retriever - Golden 6
Shepherd Dog - German 4
Pointing Dog - German Short-haired 3
Beagle 2
Pug 2
Dachshund - Miniature 2
Shepherd Dog - Australian 2
Boxer (German Boxer) 2

Most Reported Reactions

Lack of efficacy (bacteria) - Borrelia 25
Lethargy (see also Central nervous system depression in Neurological) 10
Vomiting 8
Diarrhoea 7
Not eating 7
Lack of efficacy (ectoparasite) - tick NOS 7
Lack of efficacy (bacteria) - Anaplasma 6
Lethargy (see also Central nervous system depression in 'Neurological') 5
Emesis (multiple) 5
Fever 4
Emesis 4
Not drinking 4

Outcome Breakdown

Ongoing
37 (57.8%)
Recovered/Normal
13 (20.3%)
Outcome Unknown
7 (10.9%)
Died
4 (6.3%)
Euthanized
3 (4.7%)

Lyme Adverse Event Insights

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.

Nationwide drugs with similar profiles

Two openFDA-derived peer sets for Lyme, 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 Lyme (#978 of 2,679 by report volume); death-coded 10.9%. PlainBreed drug row · report volume stamp 64 · 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 →