Total Reports
193
Above-median volume
Breed profile · FDA CVM July 2026 extract
Adverse-event filings for Norwegian Forest (Cat) in the FDA Center for Veterinary Medicine openFDA extract. Browse cat breeds, reactions, and outcomes below.
By recorded gender -- every report on file for Norwegian Forest, no filtering.
Data updated September 2026
The verdict
According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Norwegian Forest ranks #186 of 510 by total reports (193) and #108 of 275 by death-coded share (5.7%). National dual: Retriever - Labrador is #1 of 510 by total adverse-event reports (93,675) at death-coded-share rank 195 of 275 breeds with at least 50 reports (3.7%); separately, Atlantic Salmon (Salmo salar) is #1 highest death-coded share at 99.0% (report rank #233).
Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.
Release-over-release change
PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Norwegian Forest has 193 reports now versus 190 in that prior snapshot: 3 more (1.6%).
This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.
Subscribe to Norwegian Forest changesTotal Reports
193
Above-median volume
Deaths Reported
11
of 193 reports
Death-coded share of reports
5.7%
Above-median death-coded share
Avg Age at Report
8.9 yr
5.8 kg avg weight
5.7% of 193 norwegian forest reports involved a death outcome.
Read alongside breed popularity, veterinary access, and owner awareness, these shape how many events ever reach the FDA. The comparison line marks the cross-breed median death-coded share (4.8%) among breeds with 50 or more reports; values above it suggest higher reporting bias toward severe outcomes, not necessarily higher true mortality.
| Year | Reports | Trend |
|---|---|---|
| 2010 | 8 | |
| 2011 | 4 | |
| 2012 | 11 | |
| 2013 | 7 | |
| 2014 | 6 | |
| 2015 | 8 | |
| 2016 | 11 | |
| 2017 | 14 | |
| 2018 | 11 | |
| 2019 | 14 | |
| 2020 | 13 | |
| 2021 | 9 | |
| 2022 | 13 | |
| 2023 | 28 | |
| 2024 | 18 | |
| 2025 | 16 | |
| 2026 | 2 | |
Signature read: mid-pack filing volume at 193 (#186 of 510) is the scale stamp on Norwegian Forest. According to FDA CVM filings indexed on PlainBreed as of July 2026 extract, Norwegian Forest sits at #186 of 510 by report volume among all breeds and #20 of 55 among cat breeds, with 193 reports and 11 (5.7%) death-coded. On death-coded share among breeds with ≥50 reports, it ranks #108 of 275. Mean age at report: 8.9 years, average weight 5.8 kg (12.8 lbs).
Top reported signs: Vomiting (33), Lethargy (see also Central nervous system depression in 'Neurological') (27), Diarrhoea (19). Most-referenced drug: Frunevetmab (21 reports), followed by Selamectin (18) and Spinosad (18).
Outcome coding on 183 status-recorded reports is dominated by Recovered/Normal (32.2%). Annual submissions ranged 2-2,026 across 17 years on file.
Showing 6 of 54 cat breeds in our dataset, ranked by closest report volume.
Two openFDA-derived peer sets for Norwegian Forest, both outside the Cat family so the neighborhoods are not species containment (the similar-volume list above stays within species).
Nearest other-species breeds with ≥50 reports (5.7% death-coded here).
Nearest other-species breeds by reported average weight (5.8 kg here).
What to do with this cat
A report does not prove a drug caused the reaction, and popular breeds simply generate more reports.
Compare a breed's report volume against how common the breed is before drawing conclusions. See our methodology for how the death-coded share and rankings are computed, or read breed-specific reporting patterns and FDA CVM reporting.
Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025
Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →