January 2002: adverse event reports received

1,170 reports in the openFDA release of 28 Sep 2026

Read this first · FDA's caveat, in its words

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

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.

Not veterinary advice. This site lists what was reported to FDA. For an animal that is unwell, contact a veterinarian.

1,170reports received

1,415same month a year earlier-17%

1,267monthly average, preceding 12 months

55.2%concern dogscats 12%

FDA's database holds 1,170 adverse event reports received in January 2002, against 1,415 in the same month a year earlier and a monthly average of 1,267 over the preceding 12 months.

55.2% of the month's reports concern dogs, 12% cats and 3.4% horses; the rest concern other species, exposed people, or give no species.

By active ingredient, the drugs named most often were selamectin (265), moxidectin (208) and carprofen (167), and the terms listed most often were vomiting (173), accidental exposure (138) and depression (125). Report volume has a seasonal shape, with more reports in the warmer months when parasite products are in heavier use.

The months around it

Drugs named most often, by active ingredient

Active ingredients recorded for the drug	Reports	Share of the month's reports
Selamectin	265	22.6%
Moxidectin	208	17.8%
Carprofen	167	14.3%
Enrofloxacin	30	2.6%
Amoxicillin	29	2.5%
Milbemycin Oxime	28	2.4%
(S) - methoprene	28	2.4%
Ketamine Hydrochloride	27	2.3%
Ivermectin	25	2.1%
Melarsomine Dihydrochloride	24	2.1%
Etodolac	22	1.9%
Tilmicosin Phosphate	22	1.9%
Medetomidine	14	1.2%
Amitraz	12	1%
Lufenuron + Milbemycin Oxime	12	1%

Ordered by report count, which follows how widely each drug was in use. FDA states that these data cannot be used to estimate risk or to compare one product with another. Brand and manufacturer names are masked by FDA in these records.

Signs listed most often

Vomiting14.8%173
Accidental exposure[exposure that was not intended]11.8%138
Depression[dull, quiet or withdrawn]10.7%125
Death8.8%103
Anorexia[not eating]8.1%95
Ineffective, heartworm larvae[legacy FDA term: the product did not have the expected effect (heartworm larvae)]7.4%86
Vials, Leaking[a product quality report, not a sign in an animal]7.1%83
Seal, Abnormal[a product quality report, not a sign in an animal]6.7%78
Unclassifiable adverse event[event that fits no dictionary term]5.9%69
Anaphylaxis[sudden severe allergic-type reaction]5.2%61
No sign[no clinical sign was reported]5%59
Diarrhoea[diarrhea]5%58
Elevated alanine aminotransferase (ALT)[a liver enzyme above the normal range]4.2%49
Death by euthanasia[the animal was euthanized]3.8%44
Convulsion[seizure]3.5%41

Single ingredients, pooled

Selamectin22.6%265

Moxidectin17.8%208

Carprofen14.3%167

Milbemycin Oxime3.4%40

Enrofloxacin3.2%37

Ivermectin3.2%37

Amoxicillin2.5%29

(S) - methoprene2.4%28

Ketamine Hydrochloride2.3%27

Melarsomine Dihydrochloride2.1%24

Etodolac1.9%22

Tilmicosin Phosphate1.9%22

Species

Dog55.2%646

Cat12%140

Horse3.4%40

Other or not given29.4%344

Questions about January 2002

How many animal drug adverse event reports did FDA receive in January 2002?

1,170 reports are in the openFDA release of 28 Sep 2026. The same month a year earlier has 1,415.

Which drugs were named most often?

By active ingredient: selamectin (265), moxidectin (208), carprofen (167), enrofloxacin (30) and amoxicillin (29). Brands are masked in the public data.

Which signs were listed most often?

vomiting (173), accidental exposure (138), depression (125), death (103) and anorexia (95).

Can the count for a month still change?

Yes. FDA posts reports quarterly with a delay of three to six months, so the newest months are incomplete and usually grow in later releases. Older months change little.

Does a busy month mean something went wrong that month?

Not by itself. The date is when FDA received the report, not when the event happened, and volume follows season, product launches and publicity. FDA states that "there is no certainty that the reported drug or device caused the adverse event" and that the event "may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources."

Where this comes from. Counts are built from the openFDA Animal & Veterinary adverse event bulk files released 28 Sep 2026, which hold reports FDA's Center for Veterinary Medicine received through 31 Mar 2026. openFDA masks brand and manufacturer names in these files, so drugs are counted by the active ingredients each record discloses and no figure is attributed to a brand, application or company. Ingredient names, and the separate reference lists of approved products, follow the FDA Green Book as of 1 Oct 2026. The month is the date FDA first received the report, not the date of the event. No report text, lot numbers or reporter details are published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.