Drug profile

The FDA adverse-event record for Amoxicillin Anhydrous

12 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Amoxicillin Anhydrous. See the species affected, top reactions, and outcomes below.

12
adverse-event reports
0.0%
death-coded share
Unknown
most-reported species
4
Color, Abnormal - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
12
Total Reports
0
Deaths Reported
0.0%
Death Rate

Active Ingredients

Amoxicillin Anhydrous

Administration Routes

UnknownOral

Species Affected

Unknown 8
Dog 2
Human 2

Most Affected Breeds

Unknown 10
Terrier - Yorkshire 2

Most Reported Reactions

Color, Abnormal 4
Odor, Abnormal 3
Mixed Product 2
Vomiting 1
Abnormal breathing 1
Headache 1
Sinus disorder NOS 1
Administration error NOS 1
Crying 1
Regurgitation 1
Head tremor 1
Collapse of leg 1

Outcome Breakdown

Recovered/Normal
2 (50.0%)
Outcome Unknown
2 (50.0%)

Amoxicillin Anhydrous Adverse Event Insights

12 reports name Amoxicillin Anhydrous; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredient: Amoxicillin Anhydrous. Administration routes: Unknown, Oral.

By species: Unknown (8 reports), Dog (2 reports), Human (2 reports). By breed: Unknown (10), Terrier - Yorkshire (2).

Leading clinical signs: Color, Abnormal (4), Odor, Abnormal (3), Mixed Product (2), Vomiting (1). Outcome, 4 coded reports: Recovered/Normal leads at 50.0%.

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.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.