Total Reports
97
FDA CVM filings
Adverse-event records and label data for Atlantic Salmon (Salmo salar) (Fish), sourced from the FDA Center for Veterinary Medicine. Refreshed as new reports are filed. Cite PlainBreed when reusing this analysis.
Atlantic Salmon (Salmo salar) (Fish) has 97 FDA adverse event reports on record, with 96 deaths reported (9900.0% death rate) — ranking #232 by report volume. The most frequently reported reaction is Death (69 cases). The top associated drug is Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage). Average age at report: 0.7 years.
Total Reports
97
FDA CVM filings
Deaths Reported
96
of 97 reports
Death Rate
9900.0%
death-coded share
Avg Age at Report
0.7 yr
0.4 kg avg weight
9900.0% of 97 reports involved a death outcome. Read alongside breed popularity, veterinary access, and owner awareness — these shape how many events ever reach the FDA. The 12% comparison line is the rough cross-breed median in the FDA CVM database; values above suggest higher reporting bias toward severe outcomes, not necessarily higher true mortality.
| Year | Reports | Trend |
|---|---|---|
| 2015 | 2 | |
| 2016 | 16 | |
| 2017 | 12 | |
| 2018 | 7 | |
| 2019 | 10 | |
| 2020 | 16 | |
| 2021 | 14 | |
| 2022 | 9 | |
| 2023 | 10 | |
| 2024 | 1 | |
Across the FDA Center for Veterinary Medicine adverse event database, Atlantic Salmon (Salmo salar) accounts for 97 submitted reports and currently ranks #232 by report volume within the fish population. Of those reports, 96 involved a death outcome — a 9900.0% case-fatality figure calculated directly from the underlying FDA records rather than from external mortality studies. The mean age at time of reporting is 0.7 years, with an average recorded body weight of 0.4 kg (0.9 lbs). These figures reflect the voluntary reporting pool only and should be read alongside breed popularity, veterinary access, and owner awareness — all of which shape how many events ever reach the FDA.
The most frequently reported clinical signs for Atlantic Salmon (Salmo salar) are Death (69 reports), IGA Animal mortality greater than expected (41 reports), Fish body deformity (31 reports), together capturing a substantial share of the top-reaction traffic seen in this breed's record. On the product side, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) appears in 88 reports and is the single most-referenced drug, followed by Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage (7) and Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A Locus In The Eo-1A Lineage) (1). Counts like these surface which therapeutic classes dominate the reporting stream — useful context when comparing reactions across breeds of the same fish species.
Outcome coding on the 115 reports with a recorded status is dominated by Died (60.0% of coded outcomes). Annual submission volume ranges from 2,015 to 2,024 reports across the 10 years on file, indicating the reporting trend is shaped as much by awareness cycles as by underlying clinical events. Because FDA adverse event reports describe correlation rather than causation, these numbers are most useful as a signal of where to ask further questions with a veterinarian — not as a standalone risk score for any individual fish.
Atlantic Salmon (Salmo salar) has 97 adverse event reports on file. Lower report volumes may reflect a less common breed, lower reporting rates, or genuinely fewer adverse events.
The 9900.0% death rate is above average, though this statistic should be interpreted cautiously. Death reports may be overrepresented because serious outcomes are more likely to be reported than mild reactions.
The most frequently referenced drug in adverse reports is Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage), appearing in 88 reports. This may indicate widespread use of the medication rather than a specific safety concern for Atlantic Salmon (Salmo salar).
What FDA reports are and how they are collected
Why some breeds appear in more adverse event reports
Evaluating medication risks using FDA data
Drugs that appear most in adverse event reports
The reporting process and database limitations
Adverse event data sourced from the FDA Center for Veterinary Medicine via the openFDA Animal & Veterinary Adverse Events API. Reports are voluntarily submitted by pet owners, veterinarians, and product manufacturers.
Atlantic Salmon (Salmo salar) ranks #232 by total report volume. Death rate (9900.0%) reflects the proportion of reports involving death and should not be interpreted as a breed-specific mortality rate. Reporting biases, breed popularity, and veterinary access all influence report counts.
Read our methodology — how this data is sourced, computed, and verified.