Drug profile

The FDA adverse-event record for Eiv*3/W,Eev/Ehv1,4/Tet/Yf-Wnv

10 FDA reports name Eiv*3/W,Eev/Ehv1,4/Tet/Yf-Wnv, a lower-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#2574 of 2,679
by report volume (all drugs)
10
adverse-event reports
20.0%
death-coded share
Horse
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Eiv*3/W,Eev/Ehv1,4/Tet/Yf-Wnv ranks #2536 of 2679 by total reports (10). 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)
#2536
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.

Signature read: 10 reports place Eiv*3/W,Eev/Ehv1,4/Tet/Yf-Wnv in the lower third of FDA AER volume (#2574 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.
10
Total Reports
2
Deaths Reported
20.0%
Death-coded share of reports

Active Ingredients

Eiv*3/W,Eev/Ehv1,4/Tet/Yf-Wnv

Administration Routes

IntramuscularUnknown

Species Affected

Horse 10

Most Affected Breeds

Thoroughbred 2
Warmblood (unspecified) 2
Quarter Horse 1
Crossbred Equine/horse 1
Miniature 1
Lusitano 1
Morgan 1
Horse (other) 1

Most Reported Reactions

Fever 4
Injection site swelling 4
Nasal discharge 2
Injection site pain 2
Injection site lump 2
Breathing difficulty 1
Lung sound 1
Hives (see also 'Skin') 1
Lethargy (see also Central nervous system depression in 'Neurological') 1
Injection site hair loss 1
Injection site skin discolouration 1
Injection site weeping (see also 'skin') 1

Outcome Breakdown

Ongoing
5 (50.0%)
Recovered/Normal
3 (30.0%)
Died
1 (10.0%)
Euthanized
1 (10.0%)

Eiv*3/W,Eev/Ehv1,4/Tet/Yf-Wnv: 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 Eiv*3/W,Eev/Ehv1,4/Tet/Yf-Wnv (#2574 of 2,679 by report volume); death-coded 20.0%. PlainBreed drug row · report volume stamp 10 · 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 →