Pet Drug Reports

March 2009: 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 3,268 adverse event reports for animal drugs in March 2009. It received 2,609 reports in March 2008. The average of the 12 months before March 2009 is 2,947 reports for each month.

Of the 3,268 reports, 70.9% are about dogs, 9.4% are about cats and 1.7% 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, Sep 2007 to Sep 2009. The column with the outline is March 2009.

Reports by species

  • Dog70.9%2,318
  • Cat9.4%307
  • Horse1.7%55
  • Other species, or species not given18%588

Drug pages with reports received in March 2009

The table has every drug page with 10 or more reports that FDA received in March 2009, in order of name. No count decides which drug is in the table. The table has 45 drug pages.

Show the 45 drug pages
Drug pages with 10 or more reports received in March 2009, in order of name
Active ingredientsReports received in March 2009
Amoxicillin136
Atipamezole Hydrochloride16
Betamethasone Valerate + Clotrimazole + Gentamicin Sulfate13
Carprofen138
Cefovecin sodium39
Ceftiofur Hydrochloride16
Ceftiofur Sodium12
Clotrimazole + Gentamicin Sulfate + Mometasone Furoate Monohydrate13
Copper Naphthenate10
Cyclosporine138
Deracoxib63
Desoxycorticosterone Pivalate22
Dexmedetomidine hydrochloride39
Dirlotapide63
Doramectin34
Emodepside + Praziquantel35
Enrofloxacin13
Fenbendazole11
Firocoxib54
Fluoxetine hydrochloride26
Imidacloprid + Moxidectin71
Insulin23
Ivermectin107
Ivermectin + Praziquantel12
Ivermectin + Praziquantel + Pyrantel Pamoate33
Ivermectin + Pyrantel Pamoate616
Ketamine Hydrochloride11
Lufenuron + Milbemycin Oxime107
Marbofloxacin10
Maropitant39
Melarsomine Dihydrochloride84
Meloxicam83
Milbemycin Oxime318
Monensin15
Moxidectin23
Nitenpyram14
Pimobendan25
Propofol11
Pyrantel Pamoate18
Selamectin237
Spinosad183
Tiletamine Hydrochloride + Zolazepam Hydrochloride12
Tilmicosin Phosphate11
Trilostane10
Tulathromycin10

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 3,268 reports of the month.

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

  1. Ineffective, heartworm larvae[legacy FDA term: the product did not have the expected effect (heartworm larvae)]19.7%643 reports
  2. Vomiting15.1%493 reports
  3. Depression[dull, quiet or withdrawn]10.4%341 reports
  4. Anorexia[not eating]8.7%283 reports
  5. Diarrhoea[diarrhea]6.3%206 reports
  6. Ineffective, ascarids NOS[legacy FDA term: the product did not have the expected effect (ascarids nos)]4.6%151 reports
  7. Death4.6%150 reports
  8. Accidental exposure[exposure that was not intended]4%132 reports
  9. Lack of efficacy (endoparasite) - hookworm[the product did not have the expected effect: hookworms]3.9%129 reports
  10. Suspension, Abnormal[a product quality report, not a sign in an animal]3.7%120 reports
  11. Color, Abnormal[a product quality report, not a sign in an animal]3.5%113 reports
  12. Pruritus[itching]3.1%101 reports
  13. Ataxia[unsteady, uncoordinated movement]2.7%89 reports
  14. Convulsion[seizure]2.7%89 reports
Show the next 1 signs
  1. Elevated alanine aminotransferase (ALT)[a liver enzyme above the normal range]2.5%83 reports

Ingredients, all combinations

The list has every active ingredient with 10 or more reports received in March 2009, in order of name. It has 46 ingredients.

Show the 46 ingredients

The same month in other years

Cite this page

Pet Drug Reports. March 2009: adverse event reports for animal drugs. https://petdrugreports.com/month/2009-03/ 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 March 2009 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?

"Ineffective, heartworm larvae" is in 643 reports of the 3,268 reports of March 2009 (19.7%).