Drug profile

The FDA adverse-event record for Amikacin

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

#884 of 2,679
by report volume (all drugs)
78
adverse-event reports
19.2%
death-coded share
Horse
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Amikacin ranks #884 of 2679 by total reports (78) and #254 of 1130 by death-coded share (19.2%). 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
#254
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. Amikacin has 78 reports now versus 74 in that prior snapshot: 4 more (5.4%).

Report change
+4
Death-coded reports
+2
Death-coded share
+1.7 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 Amikacin changes

Signature read: death-coded report count at 15 is the most distinctive stamp on Amikacin'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
15
Deaths Reported
19.2%
Death-coded share of reports

Active Ingredients

Amikacin

Administration Routes

UnknownIntra-ArticularParenteralTopicalAuricular (Otic)OtherIntravenousIntramuscular

Species Affected

Horse 41
Dog 22
Unknown 9
Cat 6

Most Affected Breeds

Quarter Horse 17
Unknown 9
Horse (unknown) 9
Cat (unknown) 3
Crossbred Canine/dog 3
Domestic Shorthair 3
Trakehner 3
Bulldog 3
Warmblood (unspecified) 2
Oldenburg 2

Most Reported Reactions

Lameness 13
Death by euthanasia 11
Elevated blood urea nitrogen (BUN) 8
Ataxia 8
Elevated alanine aminotransferase (ALT) 8
Joint swelling 7
Lack of efficacy - NOS 7
Other abnormal test result NOS 7
Decreased appetite 7
Leucocytosis NOS 6
Swelling NOS 6
Abnormal radiograph finding 6

Outcome Breakdown

Ongoing
24 (35.3%)
Recovered/Normal
16 (23.5%)
Outcome Unknown
12 (17.6%)
Euthanized
11 (16.2%)
Died
4 (5.9%)
Recovered with Sequela
1 (1.5%)

Amikacin: 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 Amikacin, 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 Amikacin (#884 of 2,679 by report volume); death-coded 19.2%. PlainBreed drug row · death-coded report count stamp 15 · 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 →