Drug profile

The FDA adverse-event record for Penicillin G

50 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Penicillin G. Species, reactions, and outcomes follow.

#1127 of 2,679
by report volume (all drugs)
50
adverse-event reports
26.0%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Penicillin G ranks #1120 of 2679 by total reports (50) and #157 of 1130 by death-coded share (26.0%). 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)
#1120
This drug, reports of 2679
#157
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. Penicillin G has 50 reports now versus 48 in that prior snapshot: 2 more (4.2%).

Report change
+2
Death-coded reports
+1
Death-coded share
+1.0 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 Penicillin G changes

Signature read: Penicillin G's 26.0% death-coded share is among the highest in the openFDA drug corpus.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
50
Total Reports
13
Deaths Reported
26.0%
Death-coded share of reports

Active Ingredients

Penicillin G

Administration Routes

UnknownSubcutaneousIntravenousIntramuscularIntramammaryOral

Species Affected

Dog 27
Cat 8
Unknown 7
Cattle 3
Horse 2
Pig 1
Alpaca 1
Tiger 1

Most Affected Breeds

Unknown 11
Domestic Shorthair 7
Dog (unknown) 3
Retriever - Labrador 3
Pug 3
Boxer (German Boxer) 2
Shepherd Dog - German 2
Charolais 1
Dachshund (unspecified) 1
Domestic Longhair 1

Most Reported Reactions

Vomiting 13
Death by euthanasia 7
Death 6
Elevated alanine aminotransferase (ALT) 6
Seizure NOS 6
Other abnormal test result NOS 6
Anorexia 5
Lethargy (see also Central nervous system depression in 'Neurological') 5
Elevated blood urea nitrogen (BUN) 5
Potency, Low 5
Elevated serum alkaline phosphatase (SAP) 4
Weight loss 4

Outcome Breakdown

Recovered/Normal
14 (30.4%)
Ongoing
10 (21.7%)
Outcome Unknown
8 (17.4%)
Died
7 (15.2%)
Euthanized
7 (15.2%)

Penicillin G: 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.

Nationwide drugs with similar profiles

Two openFDA-derived peer sets for Penicillin G, 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 Penicillin G (#1127 of 2,679 by report volume); death-coded 26.0%. PlainBreed drug row · death-coded share stamp 26.0% · 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 →