Pet Drug Reports

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Breed · Cat

Norwegian Forest: adverse event reports

FDA breed label "Norwegian Forest" · single-breed animals only

187reports, 2001–20260.1% of cat reports
16reports, 12 months to March 202613 in the 12 months before
38.5%classed serious, as reportedall cats: 35.6%
11.2%name frunevetmaball cats: 5.1%

187 adverse event reports received by FDA describe an animal recorded as Norwegian Forest (FDA breed label "Norwegian Forest"). That is 0.1% of all reports about cats. Crossbred animals are not counted here, only reports that give this single breed.

16 reports arrived in the 12 months to March 2026, up 23% from 13 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 frunevetmab, selamectin and spinosad. Frunevetmab is named in 11.2% of this breed's reports, a larger share than in reports about all cats (5.1%).

The terms listed most often are lethargy (17.6%), vomiting (17.1%) and anorexia (10.2%). Lethargy appears in 17.6% of reports, a larger share than in all cat reports (9.7%). 38.5% of reports stating seriousness were classed as serious, against 35.6% for cats overall.

Drugs named most often, by active ingredient

Active ingredients recorded for the drugReportsShare of Norwegian Forest reportsShare of all cat reports
Frunevetmab2111.2%5.1%
Selamectin189.6%14.8%
Spinosad168.6%7.8%
Cefovecin sodium158%5.8%
Fluralaner147.5%7%
Insulin147.5%2.4%
Nitenpyram147.5%5.8%
Imidacloprid + Moxidectin115.9%5.5%
Sarolaner + Selamectin105.3%5.3%
Buprenorphine73.7%3.7%
Cyclosporine52.7%2%
Maropitant52.7%2.5%
Butorphanol Tartrate42.1%1.5%
Isoflurane42.1%1.3%
Robenacoxib42.1%2.2%
Velagliflozin42.1%2.9%
Amoxicillin31.6%1.1%
Bexagliflozin31.6%2.5%
Ketamine Hydrochloride31.6%2.5%
Methylprednisolone Acetate31.6%1%

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 Norwegian Forest reports listing the termall cat reports

  1. Lethargy[unusually tired or inactive]17.6%33
  2. Vomiting17.1%32
  3. Anorexia[not eating]10.2%19
  4. Diarrhoea[diarrhea]8.6%16
  5. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]7%13
  6. Ataxia[unsteady, uncoordinated movement]4.3%8
  7. Behavioural disorder NOS[behaviour change, type not specified]4.3%8
  8. Depression[dull, quiet or withdrawn]4.3%8
  9. Death3.7%7
  10. Elevated alanine aminotransferase (ALT)[a liver enzyme above the normal range]3.7%7
  11. Emesis[vomiting]3.7%7
  12. Lack of efficacy - NOS[the product did not have the expected effect]3.7%7
  13. Panting3.7%7
  14. Application site hair loss[hair loss where the product was applied]3.2%6
  15. Death by euthanasia[the animal was euthanized]3.2%6
  16. Fever3.2%6
  17. Hiding3.2%6
  18. Ineffective, glycemic control[legacy FDA term: the product did not have the expected effect (glycemic control)]3.2%6
  19. Pruritus[itching]3.2%6

Age and weight

Age of the animal

Under 1 year4.8%9
1 to 3 years17.6%33
4 to 7 years13.4%25
8 to 11 years28.9%54
12 years and over34.2%64
Age not given1.1%2

Weight of the animal

Under 5 kg (11 lb)39%73
5 to 9.9 kg (11–22 lb)55.1%103
10 to 24.9 kg (22–55 lb)3.2%6
25 to 44.9 kg (55–99 lb)0%0
45 kg and over (99 lb+)0%0
Weight not given2.7%5

Coloured bar: Norwegian Forest reports. Grey bar: all cat reports.

Trend and outcomes

024Apr 2021: 0May 2021: 3Jun 2021: 1Jul 2021: 0Aug 2021: 3Sep 2021: 0Oct 2021: 2Nov 2021: 0Dec 2021: 0Jan 2022: 12022Feb 2022: 0Mar 2022: 0Apr 2022: 1May 2022: 1Jun 2022: 1Jul 2022: 1Aug 2022: 1Sep 2022: 1Oct 2022: 1Nov 2022: 1Dec 2022: 0Jan 2023: 12023Feb 2023: 2Mar 2023: 1Apr 2023: 3May 2023: 3Jun 2023: 1Jul 2023: 2Aug 2023: 2Sep 2023: 3Oct 2023: 4Nov 2023: 3Dec 2023: 3Jan 2024: 22024Feb 2024: 0Mar 2024: 2Apr 2024: 1May 2024: 2Jun 2024: 2Jul 2024: 4Aug 2024: 0Sep 2024: 1Oct 2024: 1Nov 2024: 1Dec 2024: 0Jan 2025: 02025Feb 2025: 1Mar 2025: 0Apr 2025: 2May 2025: 0Jun 2025: 2Jul 2025: 1Aug 2025: 3Sep 2025: 1Oct 2025: 0Nov 2025: 2Dec 2025: 3Jan 2026: 12026Feb 2026: 0Mar 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/Normal27.8%52
Recovered with Sequela1.1%2
Ongoing28.3%53
Died5.3%10
Euthanized2.1%4
Outcome Unknown24.1%45

Beside all cats

MeasureNorwegian ForestAll cats
Reports187148,080
Latest 12 months1612,477
Classed serious, of reports stating it38.5%35.6%
Death or euthanasia recorded, per 1,000 reports74.995

Questions about Norwegian Forest reports

How many FDA adverse event reports involve Norwegian Forests?

187 reports through March 2026, 0.1% of reports about cats; 16 in the latest 12 months.

Which drugs are named most often in Norwegian Forest reports?

By active ingredient: frunevetmab (21), selamectin (18), spinosad (16), cefovecin sodium (15) and fluralaner (14). Brands are masked in the public data.

What signs are reported most for this breed?

lethargy (17.6%), vomiting (17.1%), anorexia (10.2%), diarrhoea (8.6%) and decreased appetite (7%).

Is the Norwegian Forest 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 Norwegian Forest 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 ("Norwegian Forest" becomes "Norwegian Forest"). 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.