December 1998: 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 3,078 adverse event reports for animal drugs in December 1998. It received 294 reports in December 1997. The average of the 12 months before December 1998 is 571 reports for each month.
Of the 3,078 reports, 90.1% are about dogs, 2.6% are about cats and 1.1% 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 by species
- Dog90.1%2,774
- Cat2.6%79
- Horse1.1%35
- Other species, or species not given6.2%190
Drug pages with reports received in December 1998
The table has every drug page with 10 or more reports that FDA received in December 1998, in order of name. No count decides which drug is in the table. The table has 13 drug pages.
| Active ingredients | Reports received in December 1998 |
|---|---|
| Amoxicillin | 18 |
| Ampicillin Trihydrate | 36 |
| Carprofen | 2,612 |
| Enrofloxacin | 12 |
| Eprinomectin | 10 |
| Etodolac | 38 |
| Lufenuron | 13 |
| Medetomidine | 14 |
| Moxidectin | 42 |
| Ormetoprim + Sulfadimethoxine | 57 |
| Propofol | 16 |
| Selegiline Hydrochloride | 15 |
| Tilmicosin Phosphate | 10 |
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 3,078 reports of the month.
The sign that is in the largest number of the reports comes first.
- Elevated serum alkaline phosphatase (SAP)[a liver and bone enzyme above the normal range]23.8%733 reports
- Elevated alanine aminotransferase (ALT)[a liver enzyme above the normal range]22.4%688 reports
- Anorexia[not eating]17.7%546 reports
- Vomiting17.5%538 reports
- Depression[dull, quiet or withdrawn]10%308 reports
- Elevated total bilirubin[bilirubin above the normal range]9.2%284 reports
- Diarrhoea[diarrhea]7%216 reports
- Icterus[jaundice (yellowing)]6.5%199 reports
- Elevated blood urea nitrogen (BUN)[a kidney value above the normal range]4.9%151 reports
- Convulsion[seizure]4.8%149 reports
- Elevated liver enzymes[liver enzymes above the normal range]4.4%134 reports
- Anaemia NOS[low red blood cell count]4.3%131 reports
- Elevated aspartate aminotransferase (AST)[a liver and muscle enzyme above the normal range]4.2%130 reports
- Elevated creatinine[a kidney value above the normal range]4%124 reports
Show the next 1 signs
- Accidental exposure[exposure that was not intended]3.9%121 reports
Ingredients, all combinations
The list has every active ingredient with 10 or more reports received in December 1998, in order of name. It has 17 ingredients.
The same month in other years
Cite this page
Pet Drug Reports. December 1998: adverse event reports for animal drugs. https://petdrugreports.com/month/1998-12/ 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 December 1998 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?
"Elevated serum alkaline phosphatase (SAP)" is in 733 reports of the 3,078 reports of December 1998 (23.8%).