Pet Drug Reports

January 2020: adverse event reports that FDA received

Month in which FDA received the reports

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 .

FDA received 5,295 adverse event reports for animal drugs in January 2020. It received 5,478 reports in January 2019. The average of the 12 months before January 2020 is 6,041 reports for each month.

Of the 5,295 reports, 73.3% are about dogs, 8.9% are about cats and 0.8% are about horses. The other reports are about other species, or give no species. A report is not proof that a drug caused a sign.

Search engines do not list month pages. The site keeps the page, and the list of months links it.

The months before and after

Reports for each month, Jul 2018 to Jul 2020. The column with the outline is January 2020.

Reports by species

  • Dog73.3%3,883
  • Cat8.9%473
  • Horse0.8%42
  • Other species, or species not given16.9%897

Drug pages with reports received in January 2020

The table has every drug page with 10 or more reports that FDA received in January 2020, in order of name. No count decides which drug is in the table. The table has 80 drug pages.

Show the 80 drug pages
Drug pages with 10 or more reports received in January 2020, in order of name
Active ingredientsReports received in January 2020
(S) - methoprene17
Acepromazine Maleate12
Afoxolaner306
Amoxicillin Trihydrate + Clavulanate Potassium35
Bupivacaine13
Buprenorphine13
Butorphanol Tartrate29
Capromorelin19
Carprofen85
Cefovecin sodium72
Cefpodoxime proxetil14
Ceftiofur Crystalline Free Acid13
Cephalexin11
Clotrimazole + Gentamicin13
Cyclosporine59
Deracoxib18
Desoxycorticosterone Pivalate15
Dexamethasone17
Dexmedetomidine hydrochloride18
Diphenhydramine26
Doramectin22
Doxycycline30
Emodepside + Praziquantel24
Enrofloxacin16
Eprinomectin13
Eprinomectin + Praziquantel23
Famotidine12
Febantel + Praziquantel + Pyrantel Pamoate43
Fenbendazole10
Florfenicol + Mometasone furoate + Terbinafine25
Florfenicol + Terbinafine12
Fluralaner494
Gabapentin29
Gamithromycin14
Grapiprant84
Imidacloprid21
Imidacloprid + Moxidectin106
Insulin106
Isoflurane14
Ivermectin47
Ivermectin + Praziquantel + Pyrantel Pamoate14
Ivermectin + Pyrantel Pamoate763
Ketamine Hydrochloride10
Ketoconazole18
Levothyroxine sodium14
Lotilaner104
Lufenuron + Milbemycin Oxime123
Lufenuron + Milbemycin Oxime + Praziquantel83
Maropitant73
Melarsomine Dihydrochloride115
Meloxicam53
Metronidazole16
Milbemycin Oxime46
Milbemycin Oxime + Praziquantel405
Milbemycin Oxime + Spinosad444
Mirtazapine20
Monensin14
Moxidectin576
Nitenpyram51
Oclacitinib155
Omeprazole13
Pimobendan28
Polysulfated Glycosaminoglycan42
Pradofloxacin10
Praziquantel24
Praziquantel + Pyrantel Pamoate22
Prednisolone19
Prednisone42
Propofol14
Pyrantel Pamoate16
Rabacfosadine10
Robenacoxib19
Sarolaner171
Sarolaner + Selamectin73
Selamectin106
Sodium Chloride52
Spinosad57
Telmisartan11
Trilostane104
Tulathromycin15

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.

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.

Commonly used products may have a higher number of reported adverse events due to the higher total number of animals being given the product.

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

Signs that the reports of the month 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 5,295 reports of the month.

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

  1. Vomiting16.8%892 reports
  2. Lack of efficacy (endoparasite) - heartworm[the product did not have the expected effect: heartworm]13.9%734 reports
  3. Lethargy[unusually tired or inactive]7.9%418 reports
  4. Diarrhoea[diarrhea]5.7%300 reports
  5. Ineffective, hooks[legacy FDA term: the product did not have the expected effect (hooks)]4.3%226 reports
  6. Product problem[a product quality report, not a sign in an animal]3.3%174 reports
  7. Seizure NOS[seizure, type not specified]3.2%171 reports
  8. Death3%160 reports
  9. Containers, Damaged[a product quality report, not a sign in an animal]2.7%142 reports
  10. Unpalatable[legacy FDA term: the animal would not take it]2.6%136 reports
  11. Lack of efficacy (endoparasite) - roundworm NOS[the product did not have the expected effect: roundworms]2.5%135 reports
  12. Lack of efficacy - NOS[the product did not have the expected effect]2.4%127 reports
  13. Behavioural disorder NOS[behaviour change, type not specified]2.2%118 reports
  14. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]2.2%118 reports
Show the next 1 signs
  1. Not eating2.2%117 reports

Ingredients, all combinations

The list has every active ingredient with 10 or more reports received in January 2020, in order of name. It has 76 ingredients.

Show the 76 ingredients

The same month in other years

Cite this page

Pet Drug Reports. January 2020: adverse event reports for animal drugs. https://petdrugreports.com/month/2020-01/ 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 month is the month in which FDA received the report, not the month of the event.

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 month

Can the count for January 2020 change?

Yes. 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.

Does the month show when the event occurred?

No. The month is the month in which FDA received the report. The event can be from an earlier month.

Which sign is in the largest number of the reports of the month?

"Vomiting" is in 892 reports of the 5,295 reports of January 2020 (16.8%).