Charolais: adverse event reports for animal drugs
Breed of cattle
The FDA breed label is "Charolais". The count has only the reports that give this one breed.
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 .
This page is not veterinary advice. For an animal that is ill, speak to a veterinarian.
Contacting a veterinarianHow to report to FDAFrom February 1987 to June 2026, FDA received 308 reports that give the breed Charolais. That is 1% of the reports about cattle. In the 12 months to June 2026, FDA received 2 reports for this breed.
The count has only the reports that give this one breed. Reports about crossbred animals are in the count for the species. The signs that appear in the largest number of the 308 reports are "Death", "Lack of efficacy (ectoparasite) - lice" and "Pruritus". A report is not proof that a drug caused a sign.
By number of reports in all years, this breed is number 5 of 8 breeds of cattle with a page. Fewer than 20 reports gave this breed in the 12 months before June 2026, so this page gives no change. The sign "Lack of efficacy (ectoparasite) - lice" is in 14.9% of the reports that give this breed, and in 7.4% of the reports about cattle.
Search engines list a breed page with 1,500 reports or more in all years. The page also needs 30 reports or more in the 12 months to June 2026. This page is under one of these numbers. The site keeps the page and keeps it out of search engines.
Drug pages with reports for this breed
The table has every drug page with 5 or more reports that give this breed, in order of name. No count decides which drug is in the table. The table has 12 drug pages.
| Active ingredients | Reports that give this breed |
|---|---|
| Clorsulon + Ivermectin | 11 |
| Doramectin | 45 |
| Eprinomectin | 32 |
| Florfenicol | 6 |
| Ivermectin | 82 |
| Levamisole | 7 |
| Monensin | 9 |
| Moxidectin | 21 |
| Oxytetracycline | 7 |
| Tildipirosin | 5 |
| Tilmicosin Phosphate | 20 |
| Tulathromycin | 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 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 308 reports that list the sign.
The sign that is in the largest number of the reports comes first.
- Death36.4%112 reports
- Lack of efficacy (ectoparasite) - lice[the product did not have the expected effect: lice]14.9%46 reports
- Pruritus[itching]7.5%23 reports
- Alopecia NOS[hair loss, type not specified]5.8%18 reports
- Recumbency[lying down and unable or unwilling to rise]5.8%18 reports
- Anaphylaxis[sudden severe allergic-type reaction]5.5%17 reports
- Ataxia[unsteady, uncoordinated movement]5.2%16 reports
- Collapse4.9%15 reports
- Hypersalivation[drooling]4.9%15 reports
- Ineffective, lice biting[legacy FDA term: the product did not have the expected effect (lice biting)]4.5%14 reports
- Lack of efficacy - NOS[the product did not have the expected effect]4.5%14 reports
- Depression[dull, quiet or withdrawn]4.2%13 reports
- Lack of efficacy (bacteria) - NOS[the product did not have the expected effect: target not specified]3.6%11 reports
- Death by euthanasia[the animal was euthanized]3.2%10 reports
Show the next 11 signs
- Dyspnoea[difficulty breathing]3.2%10 reports
- Fever2.9%9 reports
- Staggering2.9%9 reports
- Anorexia[not eating]2.6%8 reports
- Ineffective, parasite(s) NOS[legacy FDA term: the product did not have the expected effect (parasite(s) nos)]2.6%8 reports
- Injection site swelling[swelling where the injection was given]2.6%8 reports
- PR-lung(s), lesion(s)[legacy FDA term: lesions found in the lungs]2.6%8 reports
- Paralysis2.6%8 reports
- Ruminal bloat2.6%8 reports
- Diarrhoea[diarrhea]2.3%7 reports
- Ineffective, lice sucking[legacy FDA term: the product did not have the expected effect (lice sucking)]2.3%7 reports
What the reports record
Age of the animal
- Charolais reports
- All reports about cattle
- Under 1 year28.2%87, All reports about cattle: 19.3%
- 1 to 3 years23.4%72, All reports about cattle: 14.7%
- 4 to 7 years4.5%14, All reports about cattle: 6.5%
- 8 to 11 years1.6%5, All reports about cattle: 0.5%
- 12 years and over0.6%2, All reports about cattle: 0.1%
- Age not given41.6%128, All reports about cattle: 58.9%
Weight of the animal
- Charolais reports
- All reports about cattle
- Under 5 kg (11 lb)0%0, All reports about cattle: 0%
- 5 to 9.9 kg (11 to 22 lb)0%0, All reports about cattle: 0%
- 10 to 24.9 kg (22 to 55 lb)0%0, All reports about cattle: 0.1%
- 25 to 44.9 kg (55 to 99 lb)0%0, All reports about cattle: 0.6%
- 45 kg and over (99 lb and over)65.6%202, All reports about cattle: 53.5%
- Weight not given34.4%106, All reports about cattle: 45.7%
Outcome at the time of the report
- Recovered/Normal3.6%11
- Recovered with Sequela[recovered, with a lasting effect]1.6%5
- Ongoing2.6%8
- Died40.6%125
- Euthanized1.6%5
- Outcome Unknown10.7%33
An outcome in a report is not proof that the drug caused it. The person who sends the report gives the outcome. Each share is of the 308 reports that give this breed.
Each share of age and weight is of the 308 reports that give this breed. The thin bar is the same share in the 31,355 reports about cattle.
Reports by month and by year
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.
| Year | Reports |
|---|---|
| 2026 | 2 |
| 2025 | 2 |
| 2023 | 5 |
| 2022 | 3 |
| 2021 | 6 |
| 2020 | 10 |
| 2019 | 1 |
| 2018 | 5 |
| 2017 | 6 |
| 2016 | 12 |
| 2015 | 6 |
| 2014 | 13 |
| 2013 | 8 |
| 2012 | 5 |
| 2011 | 8 |
| 2010 | 10 |
| 2009 | 13 |
| 2008 | 12 |
| 2007 | 13 |
| 2006 | 13 |
| 2005 | 10 |
| 2004 | 11 |
| 2003 | 10 |
| 2002 | 14 |
| 2001 | 7 |
| 2000 | 8 |
| 1999 | 24 |
| 1998 | 8 |
| 1997 | 11 |
| 1996 | 9 |
| 1995 | 5 |
| 1994 | 3 |
| 1993 | 1 |
| 1992 | 1 |
| 1991 | 3 |
| 1990 | 5 |
| 1989 | 7 |
| 1988 | 9 |
| 1987 | 9 |
Next in the A to Z list of breeds
Cite this page
Pet Drug Reports. Charolais: adverse event reports for animal drugs. https://petdrugreports.com/breed/cattle/charolais/ 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 site puts the FDA breed label in the usual order of the words.
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 these reports
- What ages are the animals in the reports?
The figures are shares of the 308 reports about this breed received from February 1987 to June 2026. 28.2% give an age of under 1 year. 23.4% give an age of 1 to 3 years. 41.6% give no age.
- How does the count of the latest 12 months compare with the 12 months before?
FDA received 2 reports in the 12 months to June 2026. It received 2 reports in the 12 months before. 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.
- Why are crossbred animals not in the count?
The site counts a report for a breed only when the report gives one breed. A report for a crossbred animal can give more than one breed, and a count for each breed would count the report more than once. The reports about crossbred animals are in the count for cattle.
- Do the reports show that this breed reacts more to a drug?
No. The reports do not give the number of animals of the breed. FDA states 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.
FDA Center for Veterinary Medicine. Source: Adverse Event Reports for Animal Drugs and Devices