Drug profile

The FDA adverse-event record for Felv Vaccine

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

#886 of 2,679
by report volume (all drugs)
78
adverse-event reports
14.1%
death-coded share
Cat
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Felv Vaccine ranks #884 of 2679 by total reports (78) and #398 of 1130 by death-coded share (14.1%). 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)
#884
This drug, reports of 2679
#398
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. Felv Vaccine has 78 reports now versus 75 in that prior snapshot: 3 more (4.0%).

Report change
+3
Death-coded reports
+1
Death-coded share
+0.8 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 Felv Vaccine changes

Signature read: death-coded report count at 11 is the most distinctive stamp on Felv Vaccine'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.
78
Total Reports
11
Deaths Reported
14.1%
Death-coded share of reports

Active Ingredients

Felv Vaccine

Administration Routes

UnknownSubcutaneousParenteralIntramuscular

Species Affected

Cat 78

Most Affected Breeds

Domestic Shorthair 45
Domestic Longhair 12
Domestic Mediumhair 6
Cat (unknown) 6
Siamese 4
Siberian 1
Crossbred Feline/cat 1
Cat (other) 1
Bengal 1
Persian 1

Most Reported Reactions

Vomiting 22
Lethargy (see also Central nervous system depression in 'Neurological') 19
Weight loss 10
Anorexia 9
Behavioural disorder NOS 8
Diarrhoea 8
Not eating 8
Anaphylaxis 8
Lethargy (see also Central nervous system depression in Neurological) 8
Death 7
Emesis 6
Dehydration 6

Outcome Breakdown

Recovered/Normal
25 (32.1%)
Ongoing
21 (26.9%)
Outcome Unknown
18 (23.1%)
Died
8 (10.3%)
Euthanized
3 (3.8%)
Recovered with Sequela
3 (3.8%)

Felv 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 Felv 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 Felv Vaccine (#886 of 2,679 by report volume); death-coded 14.1%. PlainBreed drug row · death-coded report count stamp 11 · 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 →