Drug profile

The FDA adverse-event record for Famotidine

3,022 FDA reports name Famotidine, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#73 of 2,679
by report volume (all drugs)
3,022
adverse-event reports
24.0%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Famotidine ranks #73 of 2679 by total reports (3,022) and #185 of 1130 by death-coded share (24.0%). 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)
#73
This drug, reports of 2679
#185
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. Famotidine has 3,022 reports now versus 2,981 in that prior snapshot: 41 more (1.4%).

Report change
+41
Death-coded reports
+3
Death-coded share
−0.2 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 Famotidine changes

Signature read: death-coded report count at 724 is the most distinctive stamp on Famotidine'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.
3,022
Total Reports
724
Deaths Reported
24.0%
Death-coded share of reports

Active Ingredients

Famotidine

Administration Routes

UnknownOralSubcutaneousIntravenousParenteralIntramuscularOtherTopicalTransdermalIntradermal

Species Affected

Dog 2,606
Cat 404
Human 9
Parrot 2
Ferret 1

Most Affected Breeds

Retriever - Labrador 386
Domestic Shorthair 264
Crossbred Canine/dog 99
Retriever - Golden 97
Chihuahua 95
Boxer (German Boxer) 87
Terrier - Bull - American Pit 82
Terrier - Yorkshire 78
Shih Tzu 78
Shepherd Dog - German 65

Most Reported Reactions

Vomiting 887
Lethargy (see also Central nervous system depression in 'Neurological') 666
Diarrhoea 533
Anorexia 499
Death by euthanasia 427
Other abnormal test result NOS 419
Elevated alanine aminotransferase (ALT) 357
Weight loss 298
Decreased appetite 289
Not eating 280
Death 278
Elevated serum alkaline phosphatase (SAP) 270

Outcome Breakdown

Ongoing
1,008 (33.3%)
Recovered/Normal
653 (21.6%)
Outcome Unknown
604 (20.0%)
Euthanized
430 (14.2%)
Died
296 (9.8%)
Recovered with Sequela
35 (1.2%)

Famotidine: 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.

High-volume nationwide drug peers

Two openFDA-derived peer sets for Famotidine, 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 Famotidine (#73 of 2,679 by report volume); death-coded 24.0%. PlainBreed drug row · death-coded report count stamp 724 · 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 →