Pet Drug Reports

Danofloxacin (Advocin)adverse event reports that FDA received

Active ingredient

The name in brackets is a brand name with this active ingredient.

The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand.

Read this first. FDA says this about the data:

An API dataset query result cannot be used to estimate the risk associated with the product or compare one drug or device product with another. When looking at the results, be aware that there is no certainty that the reported drug or device caused the adverse event. This dataset should not be the sole source of information for clinical decision-making or other assumptions about the safety or effectiveness of a product. The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.

FDA Center for Veterinary Medicine publishes these words. Source: Adverse Event Reports for Animal Drugs and Devices, read on . The data have the reports that FDA received through .

This page is not veterinary advice. For an animal that is ill, speak to a veterinarian.

Contacting a veterinarianHow to report to FDA

From October 2002 to January 2026, FDA received 161 adverse event reports that name a drug with danofloxacin as its active ingredient. Of the 161 reports, 135 (83.9%) are about cattle. 12 reports are about people who were exposed to the drug (7.5%).

In January to March 2026, FDA received 1 report that names this drug. The signs that appear in the largest number of the 161 reports are "Death", "Lack of efficacy (bacteria) - NOS" and "Anaphylaxis". A report is not proof that a drug caused a sign.

Fewer than 20 reports named this drug in the 12 months before June 2026, so this page gives no change. Reports about cattle are 83.9% of the reports that name this drug, and 2.3% of all reports.

Search engines list a drug page with 500 reports or more in all years. The page also needs 30 reports or more in the 12 months to June 2026. This page is under one of these numbers. The site keeps the page and keeps it out of search engines.

Since the last update of the FDA data

The latest update of the FDA data, recorded on , changed no count of this page.

January to March 2026 is the latest closed quarter in the data. In that quarter FDA received 1 report that names danofloxacin: 0 dog, 0 cat, 0 horse, 1 other or not given.

All updatesFeed of updates (RSS)

Signs that the reports list

A sign is a coded term from the report. The words in brackets are a plain gloss of the term. The percentage is the share of the 161 reports that list the sign. One report can list more than one sign.

The sign that is in the largest number of the reports comes first.

  1. Death42.2%68 reports
  2. Lack of efficacy (bacteria) - NOS[the product did not have the expected effect: target not specified]27.3%44 reports
  3. Anaphylaxis[sudden severe allergic-type reaction]16.1%26 reports
  4. Lack of efficacy - NOS[the product did not have the expected effect]13%21 reports
  5. Hypersalivation[drooling]9.9%16 reports
  6. Necropsy performed8.7%14 reports
  7. Recumbency[lying down and unable or unwilling to rise]8.7%14 reports
  8. Collapse8.1%13 reports
  9. Accidental exposure[exposure that was not intended]7.5%12 reports
  10. Dyspnoea[difficulty breathing]7.5%12 reports
  11. Unclassifiable adverse event[event that fits no dictionary term]7.5%12 reports
  12. Bronchopneumonia6.8%11 reports
  13. Found dead6.8%11 reports
  14. Respiratory tract disorder NOS[NOS: not otherwise specified]6.8%11 reports
Show the next 16 signs
  1. Lung oedema6.2%10 reports
  2. Ataxia[unsteady, uncoordinated movement]5.6%9 reports
  3. Death by euthanasia[the animal was euthanized]5.6%9 reports
  4. Lameness5.6%9 reports
  5. Death-treatment failure5%8 reports
  6. Pneumonia[lung infection or inflammation]4.3%7 reports
  7. Ruminal bloat4.3%7 reports
  8. Depression[dull, quiet or withdrawn]3.7%6 reports
  9. Injection site pain[pain where the injection was given]3.7%6 reports
  10. Pulmonary emphysema3.7%6 reports
  11. Weakness3.7%6 reports
  12. Injection site swelling[swelling where the injection was given]3.1%5 reports
  13. Laboured breathing3.1%5 reports
  14. Malaise[generally unwell]3.1%5 reports
  15. Residues in meat/offal3.1%5 reports
  16. Swollen limb3.1%5 reports

The list shows 30 of 168 coded signs. A report is not proof that a drug caused a sign. Download all signs (CSV)

Reports by species

The share is of all 161 reports that name danofloxacin. The other reports give a different species or no species.

Reports for each month, Jul 2021 to Jun 2026

Dog0 reports

No chart: no month has 5 or more reports.

Cat0 reports

No chart: no month has 5 or more reports.

Horse0 reports

No chart: no month has 5 or more reports.

Other or not given39 reports. Largest count in one month: 6 (Sep 2025)

The month is the month in which FDA received the report. Each chart has its own scale. FDA says that a report can take 3 to 6 months to reach the public data. The newest months can get more reports in a later update.

Reports by year

  • Dog
  • Cat
  • Horse
  • Other or not given
Reports that name danofloxacin, by the year in which FDA received them and by species
YearDogCatHorseOther or not givenAll species
202600011
20250002323
202400044
202300099
202200011
202100011
202010056
201900022
201600022
201500044
201400033
201300066
201200033
201100033
201000033
200900044
200800077
200700077
20060001010
200500099
20040002121
20030001818
20020001414

2026 has the reports that FDA received through Jan 2026. Download the years (CSV)

What the reports record

Outcome at the time of the report

  • Recovered/Normal5.6%9
  • Recovered with Sequela[recovered, with a lasting effect]1.9%3
  • Ongoing1.9%3
  • Died55.9%90
  • Euthanized5%8
  • Outcome Unknown19.9%32

An outcome in a report is not proof that the drug caused it. The person who sends the report gives the outcome. Each share is of the 161 reports that name danofloxacin.

A report about more than one animal can have more than one outcome.

Kind of report

  • Safety issue73.9%119
  • Lack of expected effectiveness17.4%28
  • Both safety and lack of expected effectiveness2.5%4
  • Manufacturing or product defect6.2%10
  • Other0%0

58 reports say if the event was serious. 79.3% of them have the serious flag. The person who sends the report sets the flag.

Show age, weight, breed and route

Age of the animal

  • Under 1 year42.2%68
  • 1 to 3 years5.6%9
  • 4 to 7 years0%0
  • 8 to 11 years0%0
  • 12 years and over7.5%12
  • Age not given44.7%72

Weight of the animal

  • Under 5 kg (11 lb)0%0
  • 5 to 9.9 kg (11 to 22 lb)0%0
  • 10 to 24.9 kg (22 to 55 lb)1.2%2
  • 25 to 44.9 kg (55 to 99 lb)2.5%4
  • 45 kg and over (99 lb and over)63.4%102
  • Weight not given32.9%53

Breed, where the report gives one breed

A breed with many animals has many reports.

Route in the report

  • Subcutaneous65.8%106
  • Intramuscular2.5%4
  • Topical1.9%3
  • Intradermal0.6%1
  • Intravenous0.6%1
  • Oral0.6%1

Each bar is on a scale of 0 to 100%.

Approved animal drugs with this active ingredient (FDA Green Book)

This section is reference data. It has no report count.

The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand.

Brand names

  • Advocin

What the Green Book records give

Applications with an approval in force
1
Approved species
Cattle
Dose forms
Injectable Solution
Routes
Subcutaneous
Sale
RX (prescription)
Earliest approval date in the records

The species, dose forms and routes are the words of the Green Book records for all the applications together. One product can have fewer. The label of a product gives its approved use.

Applications in the Green Book of 2 Nov 2026, pioneer applications (NADA) first
Brand nameActive ingredientsSponsorApproved speciesApplication
Advocin Sterile Injectable SolutionDanofloxacinZoetis Inc.CattleNADA 141-207

Next in the A to Z list

All drugs by active ingredient. Brand names A to Z

FDA pages for this drug

The site checked these addresses on . The links open in a new tab.

Cite this page

Pet Drug Reports. Danofloxacin: adverse event reports that FDA received. https://petdrugreports.com/drug/danofloxacin/ Source: FDA Center for Veterinary Medicine, openFDA Animal and Veterinary adverse event reports, export of . Reports received through .

Where the data come from

The counts come from the openFDA Animal and Veterinary adverse event files, export of 30 Oct 2026. The files have the reports that the FDA Center for Veterinary Medicine received through 26 Jun 2026. The files mask brand and manufacturer names. The site counts a drug by the active ingredients that each record gives, and gives no count to a brand, an application or a company. Ingredient names and the lists of approved products follow the FDA Green Book of 2 Nov 2026. The site does not use the application number that a record has.

The site does not publish report text, lot numbers or details of a reporter. FDA's record is the authority. See how the site counts reports, the data sources and the corrections page.

Questions about these reports

Which brand are these reports about?

The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand. The Green Book section of this page lists the brand names with this active ingredient.

Do the reports show that the drug caused the signs?

No. FDA states this about the data.

When looking at the results, be aware that there is no certainty that the reported drug or device caused the adverse event.

The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.

FDA Center for Veterinary Medicine. Source: Adverse Event Reports for Animal Drugs and Devices

How many reports did FDA receive in the latest 12 months?

FDA received 16 reports in the 12 months to June 2026. It received 12 reports in the 12 months before. FDA says that a report can take 3 to 6 months to reach the public data. The newest months can get more reports in a later update.

What kinds of report are in the count?

Of the 161 reports received from October 2002 to January 2026, 73.9% are about a safety issue only. 19.9% are about a lack of expected effectiveness, alone or with a safety issue. 6.2% are about a defect of the product or its package.