Pet Drug Reports

Reported signs

Reported sign · VeDDRA term

Uveitis: reports listing this term

456reports listing the term, 1987–20260% of all reports
33reports, 12 months to March 202613 in the 12 months before
73.3%classed serious, as reportedall reports: 38.6%
79.2%of these reports concern dogscat 16.2%

"Uveitis" is a coded term listed in 456 adverse event reports received by FDA, 0% of the database. Terms come from VeDDRA, the veterinary dictionary that FDA and drug companies use to code what a reporter describes.

33 reports listed it in the 12 months to March 2026, up 154% from 13 in the 12 months before. FDA posts reports quarterly with a delay of three to six months, so the newest months are incomplete and usually grow in later releases.

By active ingredient, the drugs named most often in those reports are carprofen, moxidectin and insulin. That order mostly follows how many reports each has overall; the table gives the term's share within each drug's own reports as well.

79.2% of the reports concern dogs, 16.2% of the reports concern cats and 3.3% of the reports concern horses. Of reports listing this term that state seriousness, 73.3% were classed as serious; 15.4% record a death or euthanasia among the outcomes.

Drugs named most often in these reports, by active ingredient

Active ingredients recorded for the drugReports listing the termShare of that drug's own reports
Carprofen410.1%
Moxidectin360.1%
Insulin330.2%
Cyclosporine200.1%
Oclacitinib190.1%
Cefovecin sodium150.1%
Enrofloxacin150.2%
Milbemycin Oxime + Spinosad150%
Prednisone150.2%
Spinosad150%
Selamectin140%
Fluralaner130%
Ivermectin130.1%
Deracoxib120.1%
Florfenicol + Mometasone furoate + Terbinafine120.2%
Hyaluronate Sodium121.1%
Gabapentin110.1%
Dexamethasone100.3%
Doxycycline100.2%
Ivermectin + Pyrantel Pamoate100%
Pyrantel Pamoate100.2%
Sulfadimethoxine100.6%
Afoxolaner90%
Bedinvetmab90%
Firocoxib90.1%

Ordered by number of reports, which mostly tracks how many reports a drug has overall. Across the whole database the term appears in 0% of reports. A drug's presence in a report means the animal received it, not that it produced the sign; FDA states that these data cannot be used to compare one product with another. openFDA masks brand and manufacturer names in adverse event records, so the reports counted here cannot be attributed to a particular brand.

Single ingredients, pooled across combinations

Active ingredientReports listing the termShare of the ingredient's own reports
Moxidectin440%
Carprofen410.1%
Milbemycin Oxime400%
Insulin330.2%
Spinosad300%
Pyrantel Pamoate280%
Ivermectin230%
Cyclosporine200.1%
Selamectin200%
Oclacitinib190.1%
Sarolaner180%
Cefovecin sodium150.1%
Enrofloxacin150.2%
Praziquantel150%
Prednisone150.2%
Florfenicol140.1%
Sulfadimethoxine140.5%
Terbinafine140.2%
Dexamethasone130.3%
Fluralaner130%
Deracoxib120.1%
Hyaluronate Sodium121.1%
Mometasone furoate120.2%
Gabapentin110.1%
Doxycycline100.2%

Species split

Dog79.2%361
Cat16.2%74
Horse3.3%15
Cattle1.3%6

Coloured bar: share of reports listing this term. Grey bar: the species' share of all reports. The term appears in 0% of all dog reports; The term appears in 0% of all cat reports.

Trend

036Apr 2021: 2May 2021: 1Jun 2021: 1Jul 2021: 1Aug 2021: 1Sep 2021: 0Oct 2021: 1Nov 2021: 1Dec 2021: 0Jan 2022: 02022Feb 2022: 1Mar 2022: 0Apr 2022: 3May 2022: 1Jun 2022: 0Jul 2022: 3Aug 2022: 2Sep 2022: 0Oct 2022: 1Nov 2022: 1Dec 2022: 2Jan 2023: 32023Feb 2023: 0Mar 2023: 2Apr 2023: 4May 2023: 0Jun 2023: 0Jul 2023: 0Aug 2023: 0Sep 2023: 2Oct 2023: 0Nov 2023: 0Dec 2023: 2Jan 2024: 32024Feb 2024: 0Mar 2024: 0Apr 2024: 1May 2024: 1Jun 2024: 2Jul 2024: 1Aug 2024: 0Sep 2024: 0Oct 2024: 0Nov 2024: 0Dec 2024: 1Jan 2025: 52025Feb 2025: 1Mar 2025: 1Apr 2025: 5May 2025: 2Jun 2025: 0Jul 2025: 4Aug 2025: 0Sep 2025: 3Oct 2025: 5Nov 2025: 3Dec 2025: 2Jan 2026: 62026Feb 2026: 1Mar 2026: 2

Reports by month FDA received them, five years to March 2026. The newest months are incomplete because FDA posts reports with a delay of three to six months.

016311987: 119871988: 41989: 11990: 11991: 319911992: 11994: 11995: 11996: 419961997: 31998: 71999: 32000: 1020002001: 122002: 42003: 182004: 1620042005: 132006: 132007: 192008: 1920082009: 132010: 152011: 152012: 1520122013: 192014: 262015: 152016: 2620162017: 202018: 172019: 152020: 1920202021: 112022: 142023: 132024: 920242025: 312026: 9

Outcomes and ages in these reports

Outcome recorded in the report

Recovered/Normal7.7%35
Recovered with Sequela5.9%27
Ongoing23.9%109
Died10.5%48
Euthanized4.8%22
Outcome Unknown12.1%55

Age of the animal

Under 1 year13.4%61
1 to 3 years16.9%77
4 to 7 years23.7%108
8 to 11 years28.7%131
12 years and over14%64
Age not given3.3%15
MeasureReports listing this termAll reports
Reports4561,357,245
Classed serious, of reports stating it73.3%38.6%
Death or euthanasia recorded, per 1,000 reports153.563.8

Grey bars and the right-hand column are the whole database. Outcomes are as stated by the reporter and describe the report as a whole, not this term alone.

Questions about "Uveitis"

What does "Uveitis" mean in an adverse event report?

It is a VeDDRA dictionary term picked to code what the reporter described. The report's free-text description is not published by FDA and is not shown here.

How many reports list uveitis?

456 reports through March 2026 (0% of all reports), 33 of them in the latest 12 months.

Which drugs are named most often alongside this term?

By active ingredient: carprofen (41), moxidectin (36), insulin (33), cyclosporine (20) and oclacitinib (19). Drugs with many reports overall lead almost every term's list. Brands cannot be identified: openFDA masks them.

Which species are involved?

dog (79.2%), cat (16.2%), horse (3.3%) and cattle (1.3%).

Does a drug appearing here mean it produced this sign?

No such conclusion can be drawn. 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."

My animal shows this sign. What now?

This site cannot assess an animal. A veterinarian can; for an emergency, contact a veterinary emergency clinic. See the guide on when to call a vet.

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 30 Sep 2026. Spelling variants of the same VeDDRA term (for example with and without a cross-reference note) are pooled. 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.