Pet Drug Reports

Elevated cholesterol (total): in adverse event reports for animal drugs

Clinical sign, a VeDDRA term

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 March 1987 to June 2026, FDA received 3,295 adverse event reports for animal drugs that list this sign. That is 0.2% of the 1,378,761 reports that FDA received from January 1987 to June 2026. In the 12 months to June 2026, FDA received 357 reports that list this sign.

Of the 3,295 reports, 83.6% are about dogs. A report can list more than one sign and more than one drug. A report is not proof that a drug caused a sign.

By number of reports in all years, this sign is number 195 of 1,149 clinical signs with a page. Reports that list this sign rose by 13.0% 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 83.6% of the reports that list this sign, and 72.6% of all reports.

Drug pages with reports that list this sign

The table has every drug page with 20 or more reports that list this sign, in order of name. No count decides which drug is in the table. The table has 60 drug pages.

Show the 60 drug pages
Drug pages with 20 or more reports that list this sign, in order of name
Active ingredientsReports that list the sign
Afoxolaner126
Amoxicillin53
Amoxicillin + Clavulanate Potassium29
Amoxicillin Trihydrate + Clavulanate Potassium28
Bedinvetmab110
Bexagliflozin134
Buprenorphine34
Butorphanol Tartrate34
Capromorelin28
Carprofen699
Cefovecin sodium70
Cefpodoxime proxetil26
Clomipramine Hydrochloride30
Cyclosporine119
Deracoxib183
Dexamethasone32
Diphenhydramine23
Doxycycline37
Enalapril Maleate22
Enrofloxacin45
Famotidine39
Firocoxib63
Fluralaner151
Frunevetmab22
Gabapentin121
Grapiprant60
Ilunocitinib34
Insulin109
Ivermectin40
Ivermectin + Pyrantel Pamoate96
Levothyroxine sodium26
Lotilaner30
Lufenuron + Milbemycin Oxime33
Maropitant143
Melarsomine Dihydrochloride26
Meloxicam63
Methylprednisolone Acetate21
Metoclopramide22
Metronidazole41
Milbemycin Oxime31
Milbemycin Oxime + Praziquantel53
Milbemycin Oxime + Spinosad82
Mirtazapine22
Moxidectin89
Oclacitinib205
Ondansetron30
Oxibendazole23
Pimobendan28
Polysulfated Glycosaminoglycan44
Prednisone53
Pyrantel Pamoate + Sarolaner37
Sarolaner23
Selamectin53
Selegiline Hydrochloride29
Spinosad43
Tramadol32
Trazodone21
Trilostane312
Ursodiol29
Velagliflozin184

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. A report can name more than one drug.

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.

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

Ingredients, all combinations

The list has every active ingredient with 20 or more reports that list this sign, in order of name. It has 61 ingredients.

Show the 61 ingredients

Reports by species

The share is of the 3,295 reports that list this sign. The sign is in 0.3% of all reports about the species dog. The sign is in 0.4% of all reports about the species cat.

Reports by month and by year

Reports for each month, Jul 2021 to Jun 2026. The month is the month in which FDA received the report.

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 that list Elevated cholesterol (total), by the year in which FDA received them
YearReports
2026185
2025343
2024276
202399
2022104
202199
2020105
2019107
2018149
2017156
2016136
2015118
201477
201353
201271
201164
201073
200966
200887
2007118
2006128
200599
2004135
200346
200229
200135
200091
199999
199880
199716
19965
19954
19922
19914
19902
19897
198821
19876

What these reports record

Outcome at the time of the report

  • Reports with this sign
  • All reports
  • Recovered/Normal4%132, All reports: 20.7%
  • Recovered with Sequela[recovered, with a lasting effect]1.6%53, All reports: 2.3%
  • Ongoing24.5%808, All reports: 17.4%
  • Died11.5%379, All reports: 4.9%
  • Euthanized8.3%272, All reports: 1.5%
  • Outcome Unknown21.7%714, All reports: 22.7%

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 3,295 reports that list this sign.

Age of the animal

  • Reports with this sign
  • All reports
  • Under 1 year2.6%87, All reports: 9.5%
  • 1 to 3 years6.8%223, All reports: 23.9%
  • 4 to 7 years20.5%675, All reports: 20.2%
  • 8 to 11 years40.7%1,341, All reports: 15.4%
  • 12 years and over28.2%929, All reports: 10.7%
  • Age not given1.2%40, All reports: 20.3%

The outcome is for the full report, not for this sign only.

Next in the A to Z list of signs

All clinical signs

Cite this page

Pet Drug Reports. Elevated cholesterol (total): adverse event reports for animal drugs. https://petdrugreports.com/reaction/elevated-cholesterol-total/ 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 counts the different spellings of one VeDDRA term together.

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 this sign

What does this term mean in a report?

It is a term from VeDDRA, the list of terms that FDA and drug companies use to code a report. The person who coded the report selected the term.

How does the count of the latest 12 months compare with the 12 months before?

FDA received 357 reports in the 12 months to June 2026. It received 316 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.

How many of these reports have a serious flag?

Of the 2,043 reports that say if the event was serious, 61.7% have the serious flag. The person who sends a report sets the flag.

Does a drug in the table cause this sign?

The reports do not show that. A report can name more than one drug. 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