Pet Drug Reports

Species › Horse

Breed · Horse

Arab: adverse event reports

FDA breed label "Arab" · single-breed animals only

822reports, 1987–20264.5% of horse reports
23reports, 12 months to March 202628 in the 12 months before
45%classed serious, as reportedall horses: 44.1%
21.4%name ivermectin + praziquantelall horses: 14.4%

FDA's database holds 822 reports where the animal's breed is given as "Arab", shown here as Arab: 4.5% of reports about horses. Reports on crossbred animals are left out of breed pages.

23 reports arrived in the 12 months to March 2026, down 18% from 28 in the 12 months before. A breed's count mostly mirrors how common the breed is; registration and ownership figures by breed are not public data, so no per-animal rate can be given.

By active ingredient, the drugs named most often are ivermectin + praziquantel, pergolide mesylate and omeprazole. Ivermectin + Praziquantel is named in 21.4% of this breed's reports, a larger share than in reports about all horses (14.4%).

The terms listed most often are abdominal pain (10.9%), lip oedema (8.3%) and anorexia (8.2%). Abdominal pain appears in 10.9% of reports, a larger share than in all horse reports (6.6%). 45% of reports stating seriousness were classed as serious, against 44.1% for horses overall.

Drugs named most often, by active ingredient

Active ingredients recorded for the drugReportsShare of Arab reportsShare of all horse reports
Ivermectin + Praziquantel17621.4%14.4%
Pergolide mesylate10913.3%6.5%
Omeprazole597.2%9.9%
Detomidine Hydrochloride587.1%5.6%
Moxidectin526.3%7.4%
Pyrantel Tartrate516.2%4%
Ivermectin364.4%4.6%
Flunixin Meglumine263.2%3.5%
Ceftiofur Crystalline Free Acid242.9%4.8%
Firocoxib182.2%2.6%
Moxidectin + Praziquantel131.6%2%
Pyrantel Pamoate131.6%1.1%
Xylazine111.3%2.4%
Ketamine Hydrochloride101.2%3.3%
Oxibendazole101.2%1.1%
Sucralfate101.2%1.7%
Mebendazole + Trichlorfon91.1%0.4%
Phenylbutazone91.1%0.8%
Butorphanol Tartrate70.9%1.6%
Clodronate70.9%1.7%

Ordered by report count. Differences from the species column often come from body size (which drugs a breed is prescribed) and from how common the breed was in the years a drug sold most. 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 in reports

share of Arab reports listing the termall horse reports

  1. Anorexia[not eating]8.2%67
  2. Application site swelling[swelling where the product was applied]6.6%54
  3. Death6.6%54
  4. Diarrhoea[diarrhea]6.3%52
  5. Depression[dull, quiet or withdrawn]5.6%46
  6. Death by euthanasia[the animal was euthanized]5.5%45
  7. Lack of efficacy - NOS[the product did not have the expected effect]5.4%44
  8. Ataxia[unsteady, uncoordinated movement]4.3%35
  9. Colic4.3%35
  10. Recumbency[lying down and unable or unwilling to rise]4.1%34
  11. Ineffective, gastric ulcer(s)[legacy FDA term: the product did not have the expected effect (gastric ulcer(s))]3.5%29
  12. Anaphylaxis[sudden severe allergic-type reaction]3.4%28
  13. Collapse3.4%28
  14. Urticaria[hives]3.4%28
  15. Behavioural disorder NOS[behaviour change, type not specified]3.3%27
  16. Lethargy[unusually tired or inactive]3.2%26
  17. Injection site swelling[swelling where the injection was given]2.9%24
  18. Fever2.8%23
  19. Hypersalivation[drooling]2.6%21
  20. Tachycardia[fast heart rate]2.6%21
  21. Lameness2.4%20
  22. Tachypnoea[fast breathing]2.4%20

Age and weight

Age of the animal

Under 1 year3.6%30
1 to 3 years5%41
4 to 7 years12.5%103
8 to 11 years12%99
12 years and over53.5%440
Age not given13.3%109

Weight of the animal

Under 5 kg (11 lb)0%0
5 to 9.9 kg (11–22 lb)0%0
10 to 24.9 kg (22–55 lb)0.1%1
25 to 44.9 kg (55–99 lb)0%0
45 kg and over (99 lb+)74.1%609
Weight not given25.8%212

Coloured bar: Arab reports. Grey bar: all horse reports.

Trend and outcomes

035Apr 2021: 3May 2021: 1Jun 2021: 2Jul 2021: 1Aug 2021: 0Sep 2021: 3Oct 2021: 0Nov 2021: 0Dec 2021: 1Jan 2022: 02022Feb 2022: 0Mar 2022: 1Apr 2022: 0May 2022: 1Jun 2022: 0Jul 2022: 1Aug 2022: 0Sep 2022: 1Oct 2022: 0Nov 2022: 4Dec 2022: 0Jan 2023: 02023Feb 2023: 4Mar 2023: 1Apr 2023: 1May 2023: 2Jun 2023: 0Jul 2023: 4Aug 2023: 1Sep 2023: 3Oct 2023: 3Nov 2023: 4Dec 2023: 0Jan 2024: 22024Feb 2024: 4Mar 2024: 4Apr 2024: 2May 2024: 3Jun 2024: 1Jul 2024: 4Aug 2024: 3Sep 2024: 3Oct 2024: 3Nov 2024: 0Dec 2024: 1Jan 2025: 22025Feb 2025: 5Mar 2025: 1Apr 2025: 3May 2025: 2Jun 2025: 1Jul 2025: 2Aug 2025: 2Sep 2025: 1Oct 2025: 1Nov 2025: 5Dec 2025: 1Jan 2026: 32026Feb 2026: 1Mar 2026: 1

Reports by month FDA received them. The newest months are incomplete because FDA posts reports with a delay of three to six months.

Outcome recorded in the report

Recovered/Normal17.8%146
Recovered with Sequela0.1%1
Ongoing5.6%46
Died10.2%84
Euthanized3.3%27
Outcome Unknown15.2%125

Beside all horses

MeasureArabAll horses
Reports82218,382
Latest 12 months23898
Classed serious, of reports stating it45%44.1%
Death or euthanasia recorded, per 1,000 reports133.8136

Questions about Arab reports

How many FDA adverse event reports involve Arabs?

822 reports through March 2026, 4.5% of reports about horses; 23 in the latest 12 months.

Which drugs are named most often in Arab reports?

By active ingredient: ivermectin + praziquantel (176), pergolide mesylate (109), omeprazole (59), detomidine hydrochloride (58) and moxidectin (52). Brands are masked in the public data.

What signs are reported most for this breed?

abdominal pain (10.9%), lip oedema (8.3%), anorexia (8.2%), application site swelling (6.6%) and death (6.6%).

Is the Arab more sensitive to certain drugs?

Report counts cannot answer that. They show what was reported, not what a drug did, and they are not adjusted for how many Arab animals exist or were treated. Breed-related drug sensitivities that are established are described on FDA-approved labels; a veterinarian is the person to ask about an individual animal.

Why are crossbreds not included?

FDA records crossbred animals with one or more component breeds. Counting them under each component would double count, so breed pages use single-breed reports only. Crossbreds remain in the species totals.

How do I report a problem?

Call the drug company using the number on the label, or send Form FDA 1932a to FDA. See the guide on how to report.

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. Breed names are FDA's labels rearranged into everyday order ("Arab" becomes "Arab"). 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.