Pet Drug Reports

Dexamethasone + Neomycin Sulfate + Thiabendazole (Tresaderm Dermatologic)adverse event reports that FDA received

Combination of 3 active ingredients

The name in brackets is a brand name with these active ingredients.

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 September 2011 to June 2026, FDA received 1,137 adverse event reports that name this drug. Its active ingredients are dexamethasone, neomycin sulfate and thiabendazole. Of the 1,137 reports, 584 (51.4%) are about cats. 281 reports are about dogs (24.7%).

In January to March 2026, FDA received 66 reports that name this drug. The signs that appear in the largest number of the 1,137 reports are "Lethargy", "Vomiting" and "Elevated alanine aminotransferase (ALT)". A report is not proof that a drug caused a sign.

Reports that name this drug rose by 33.8% in the 12 months to June 2026, compared with the 12 months before. Reports for all animal drugs fell by 4.6% in the same periods. The newest months can get more reports in a later update. Reports about dogs are 24.7% of the reports that name this drug, and 72.6% of all reports.

Since the last update of the FDA data

The site recorded an update of the FDA data on . FDA changed these counts for January to March 2026:

  • All species: from 42 to 66.
  • Cat: from 29 to 40.
  • Other species or species not given: from 7 to 20.

January to March 2026 is the latest closed quarter in the data. In that quarter FDA received 66 reports that name dexamethasone + neomycin sulfate + thiabendazole: 6 dog, 40 cat, 0 horse, 20 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 1,137 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. Lethargy[unusually tired or inactive]17%193 reports
  2. Vomiting9.1%104 reports
  3. Elevated alanine aminotransferase (ALT)[a liver enzyme above the normal range]6.2%70 reports
  4. Not eating6.1%69 reports
  5. Vials, Damaged[a product quality report, not a sign in an animal]5.9%67 reports
  6. Lack of efficacy - NOS[the product did not have the expected effect]5.5%63 reports
  7. Anorexia[not eating]5.4%61 reports
  8. Weight loss4.7%53 reports
  9. Other abnormal test result NOS[abnormal laboratory result, type not specified]4.6%52 reports
  10. Death by euthanasia[the animal was euthanized]4.5%51 reports
  11. Ataxia[unsteady, uncoordinated movement]4.2%48 reports
  12. Elevated total bilirubin[bilirubin above the normal range]3.8%43 reports
  13. Behavioural disorder NOS[behaviour change, type not specified]3.7%42 reports
  14. Closure, Abnormal[a product quality report, not a sign in an animal]3.7%42 reports
Show the next 16 signs
  1. Diarrhoea[diarrhea]3.7%42 reports
  2. Containers, Leaking[a product quality report, not a sign in an animal]3.4%39 reports
  3. Decreased appetite3.4%39 reports
  4. Underdose[less than the labelled amount was given]3.4%39 reports
  5. Seizure NOS[seizure, type not specified]3.1%35 reports
  6. Hyperglycaemia[high blood sugar]3%34 reports
  7. Death2.8%32 reports
  8. Fever2.8%32 reports
  9. Hiding2.8%32 reports
  10. Inappetence[reduced appetite]2.7%31 reports
  11. Seal, Abnormal[a product quality report, not a sign in an animal]2.7%31 reports
  12. Drug administration duration too long2.5%28 reports
  13. Eye irritation2.5%28 reports
  14. Vocalisation[crying out or unusual noise]2.4%27 reports
  15. Neutrophilia[high neutrophil count]2.3%26 reports
  16. Accidental exposure[exposure that was not intended]2.2%25 reports

The list shows 30 of 840 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 1,137 reports that name dexamethasone + neomycin sulfate + thiabendazole. The other reports give a different species or no species.

Reports for each month, Jul 2021 to Jun 2026

Dog79 reports. Largest count in one month: 5 (Dec 2025)
Cat351 reports. Largest count in one month: 15 (Feb 2026)
Horse0 reports

No chart: no month has 5 or more reports.

Other or not given132 reports. Largest count in one month: 10 (Jan 2026)

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 dexamethasone + neomycin sulfate + thiabendazole, by the year in which FDA received them and by species
YearDogCatHorseOther or not givenAll species
202695402891
202523104021148
20241879019116
202394002473
2022115402893
2021245502099
20204239030111
20193851035124
20184034039113
2017312601673
2016131401239
2015590014
2014580013
2013790016
2012580013
201110001

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

What the reports record

Outcome at the time of the report

  • Recovered/Normal13.9%158
  • Recovered with Sequela[recovered, with a lasting effect]0.2%2
  • Ongoing18.4%209
  • Died3.3%38
  • Euthanized4.4%50
  • Outcome Unknown41.9%476

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 1,137 reports that name dexamethasone + neomycin sulfate + thiabendazole.

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

Kind of report

  • Safety issue73.1%831
  • Lack of expected effectiveness3.2%36
  • Both safety and lack of expected effectiveness5.3%60
  • Manufacturing or product defect18.2%207
  • Other0.3%3

931 reports say if the event was serious. 34.9% 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 year10.5%119
  • 1 to 3 years14.3%163
  • 4 to 7 years15%171
  • 8 to 11 years15.7%179
  • 12 years and over18.9%215
  • Age not given25.5%290

Weight of the animal

  • Under 5 kg (11 lb)33.1%376
  • 5 to 9.9 kg (11 to 22 lb)23.5%267
  • 10 to 24.9 kg (22 to 55 lb)6.9%79
  • 25 to 44.9 kg (55 to 99 lb)4.1%47
  • 45 kg and over (99 lb and over)3.6%41
  • Weight not given28.8%327

Breed, where the report gives one breed

A breed with many animals has many reports.

Route in the report

  • Auricular (Otic)45.1%513
  • Topical12.3%140
  • Ophthalmic6.9%78
  • Other2.4%27
  • Intraocular1.4%16
  • Oral1.1%12

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

Approved animal drugs with these active ingredients (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

  • Tresaderm Dermatologic

What the Green Book records give

Applications with an approval in force
2
Approved species
Cats, Dogs
Dose forms
Liquid (Solution), Solution
Routes
Topical
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
Tresaderm Dermatologic SolutionDexamethasone, Neomycin Sulfate, ThiabendazoleBoehringer Ingelheim Animal Health USA, Inc.Dogs, CatsNADA 042-633
Thiabendazole, Dexamethasone, Neomycin Sulfate SolutionDexamethasone, Neomycin Sulfate, ThiabendazoleDechra Veterinary Products LLCDogs, CatsANADA 200-565

Other pages with one of these ingredients

A report names a drug by its set of active ingredients. Each set has its own page. The list is in order of name.

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. Dexamethasone + Neomycin Sulfate + Thiabendazole: adverse event reports that FDA received. https://petdrugreports.com/drug/dexamethasone-neomycin-sulfate-thiabendazole/ Source: FDA Center for Veterinary Medicine, openFDA Animal and Veterinary adverse event reports, export of . Reports received through .

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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 these active ingredients.

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 174 reports in the 12 months to June 2026. It received 130 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 1,137 reports received from September 2011 to June 2026, 73.1% are about a safety issue only. 8.4% are about a lack of expected effectiveness, alone or with a safety issue. 18.2% are about a defect of the product or its package.