Pet Drug Reports

February 2012: 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 4,236 adverse event reports for animal drugs in February 2012. It received 2,705 reports in February 2011. The average of the 12 months before February 2012 is 4,193 reports for each month.

Of the 4,236 reports, 74.5% are about dogs, 6.9% are about cats and 1.6% 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, Aug 2010 to Aug 2012. The column with the outline is February 2012.

Reports by species

  • Dog74.5%3,155
  • Cat6.9%294
  • Horse1.6%68
  • Other species, or species not given17%719

Drug pages with reports received in February 2012

The table has every drug page with 10 or more reports that FDA received in February 2012, in order of name. No count decides which drug is in the table. The table has 53 drug pages.

Show the 53 drug pages
Drug pages with 10 or more reports received in February 2012, in order of name
Active ingredientsReports received in February 2012
Amoxicillin28
Amoxicillin Trihydrate + Clavulanate Potassium10
Atipamezole Hydrochloride15
Betamethasone Valerate + Clotrimazole + Gentamicin Sulfate10
Carprofen117
Cefovecin sodium46
Ceftiofur Crystalline Free Acid20
Cephalexin25
Clomipramine Hydrochloride54
Clotrimazole + Gentamicin Sulfate + Mometasone Furoate Monohydrate16
Cyclosporine148
Deracoxib57
Dexmedetomidine hydrochloride27
Diphenhydramine11
Doramectin51
Emodepside + Praziquantel26
Enrofloxacin30
Eprinomectin10
Febantel + Praziquantel + Pyrantel Pamoate23
Fenbendazole34
Firocoxib51
Fluoxetine hydrochloride26
Hydroxyzine11
Imidacloprid + Moxidectin144
Insulin24
Ivermectin134
Ivermectin + Praziquantel + Pyrantel Pamoate29
Ivermectin + Pyrantel Pamoate441
Ketoconazole11
Levothyroxine sodium13
Lufenuron + Milbemycin Oxime108
Maropitant42
Melarsomine Dihydrochloride116
Meloxicam140
Milbemycin Oxime262
Milbemycin Oxime + Spinosad965
Monensin18
Moxidectin75
Nitenpyram21
Orbifloxacin13
Phenobarbital13
Pimobendan24
Praziquantel + Pyrantel Pamoate33
Prednisone27
Propofol27
Pyrantel Pamoate37
Ractopamine Hydrochloride11
Selamectin177
Spinosad611
Tiletamine Hydrochloride + Zolazepam Hydrochloride22
Tramadol30
Trilostane43
Tulathromycin18

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 4,236 reports of the month.

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

  1. Emesis[vomiting]18.8%795 reports
  2. Vomiting11.7%495 reports
  3. Lethargy[unusually tired or inactive]8.1%342 reports
  4. Ineffective, heartworm larvae[legacy FDA term: the product did not have the expected effect (heartworm larvae)]7.9%333 reports
  5. Diarrhoea[diarrhea]6.5%275 reports
  6. Anorexia[not eating]5.5%233 reports
  7. Uncoded sign[a sign with no matching dictionary term]4.6%194 reports
  8. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]4.6%193 reports
  9. Unpalatable[legacy FDA term: the animal would not take it]3.7%156 reports
  10. Digestive tract disorder NOS[digestive problem, type not specified]3.6%154 reports
  11. Death3.5%150 reports
  12. Lack of efficacy - NOS[the product did not have the expected effect]3.5%150 reports
  13. Ineffective, ascarids NOS[legacy FDA term: the product did not have the expected effect (ascarids nos)]3.5%148 reports
  14. Depression[dull, quiet or withdrawn]3.1%133 reports
Show the next 1 signs
  1. Lack of efficacy (endoparasite) - hookworm[the product did not have the expected effect: hookworms]3%126 reports

Ingredients, all combinations

The list has every active ingredient with 10 or more reports received in February 2012, in order of name. It has 58 ingredients.

Show the 58 ingredients

The same month in other years

Cite this page

Pet Drug Reports. February 2012: adverse event reports for animal drugs. https://petdrugreports.com/month/2012-02/ 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 February 2012 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?

"Emesis" is in 795 reports of the 4,236 reports of February 2012 (18.8%).