Drug profile

The FDA adverse-event record for Orbifloxacin Tablets

33 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Orbifloxacin Tablets. Species, reactions, and outcomes follow.

#1380 of 2,679
by report volume (all drugs)
33
adverse-event reports
21.2%
death-coded share
Dog
most-reported species
Verify with FDA CVM →

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Orbifloxacin Tablets ranks #1367 of 2679 by total reports (33). Death-coded-share rank requires at least 50 reports. 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)
#1367
This drug, reports of 2679

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. Orbifloxacin Tablets has 33 reports now versus 33 in that prior snapshot: 0 the same number of (0.0%).

Report change
+0
Death-coded reports
+0
Death-coded share
+0.0 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 Orbifloxacin Tablets changes

Signature read: Orbifloxacin Tablets's 21.2% 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.
33
Total Reports
7
Deaths Reported
21.2%
Death-coded share of reports

Active Ingredients

Orbifloxacin Tablets

Administration Routes

OralUnknown

Species Affected

Dog 13
Unknown 12
Cat 8

Most Affected Breeds

Unknown 12
Domestic Shorthair 6
Crossbred Canine/dog 3
Pit Bull 2
Cat (unknown) 1
Russian 1
Shih Tzu 1
Pug 1
Chihuahua 1
Dog (unknown) 1

Most Reported Reactions

Lot # and /or Expiration date missing 9
Lethargy (see also Central nervous system depression in 'Neurological') 6
Product problem 4
Death by euthanasia 4
Seizure NOS 3
Dilated pupils 3
Elevated serum alkaline phosphatase (SAP) 3
Tablets, Abnormal 3
Blindness 3
Product label issues 3
Leucocytosis NOS 2
Anorexia 2

Outcome Breakdown

Ongoing
6 (28.6%)
Euthanized
5 (23.8%)
Outcome Unknown
3 (14.3%)
Recovered with Sequela
3 (14.3%)
Died
2 (9.5%)
Recovered/Normal
2 (9.5%)

Orbifloxacin Tablets: 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.

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 Orbifloxacin Tablets (#1380 of 2,679 by report volume); death-coded 21.2%. PlainBreed drug row · death-coded share stamp 21.2% · 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 →