Drug profile

The FDA adverse-event record for Cefpodoxime

1,285 FDA reports name Cefpodoxime, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#154 of 2,679
by report volume (all drugs)
1,285
adverse-event reports
10.0%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Cefpodoxime ranks #154 of 2679 by total reports (1,285) and #549 of 1130 by death-coded share (10.0%). 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)
#154
This drug, reports of 2679
#549
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. Cefpodoxime has 1,285 reports now versus 1,222 in that prior snapshot: 63 more (5.2%).

Report change
+63
Death-coded reports
+9
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 Cefpodoxime changes

Signature read: 1,285 reports place Cefpodoxime in the upper third of FDA AER volume (#154 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.
1,285
Total Reports
128
Deaths Reported
10.0%
Death-coded share of reports

Active Ingredients

Cefpodoxime

Administration Routes

OralUnknownSubcutaneousTopicalIntravenousIntraocular

Species Affected

Dog 1,250
Cat 26
Unknown 7
Human 2

Most Affected Breeds

Retriever - Labrador 152
Shepherd Dog - German 75
Retriever - Golden 74
Crossbred Canine/dog 65
Terrier - Bull - American Pit 47
Pit Bull 40
Shih Tzu 36
Boxer (German Boxer) 29
Beagle 28
Bulldog - French 27

Most Reported Reactions

Vomiting 192
Lack of efficacy - NOS 144
Lethargy (see also Central nervous system depression in 'Neurological') 131
Other abnormal test result NOS 116
Diarrhoea 106
Lethargy (see also Central nervous system depression in Neurological) 94
Seizure NOS 85
Anorexia 79
Death by euthanasia 78
Elevated alanine aminotransferase (ALT) 77
Emesis 66
Decreased appetite 63

Outcome Breakdown

Ongoing
559 (43.8%)
Recovered/Normal
305 (23.9%)
Outcome Unknown
269 (21.1%)
Euthanized
75 (5.9%)
Died
53 (4.2%)
Recovered with Sequela
15 (1.2%)

Cefpodoxime: 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 Cefpodoxime, 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 Cefpodoxime (#154 of 2,679 by report volume); death-coded 10.0%. PlainBreed drug row · report volume stamp 1,285 · 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 →