Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage)

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89 adverse event reports submitted to the FDA

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
89
Total Reports
87
Deaths Reported
9780.0%
Death Rate

Active Ingredients

Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage)

Administration Routes

Unknown

Species Affected

Fish 88
Unknown 1

Most Affected Breeds

Atlantic Salmon (Salmo salar) 88
Unknown 1

Most Reported Reactions

Death 63
IGA Animal mortality greater than expected 35
Fish body deformity 28
Moribund 24
IGA Animal morbidity greater than expected 17
Death by euthanasia 14
Partial lack of efficacy 2
Product Defect, General 2
Genotypic test failure (IGA) 2
Unrelated death 1
Fungal skin infection NOS 1
Containment system or component failure (IGA) 1

Outcome Breakdown

Died
63 (59.4%)
Euthanized
39 (36.8%)
Ongoing
4 (3.8%)

Data Summary

Metric Value
Total adverse event reports 89
Reports involving death 87
Case-fatality rate (reported events) 9780.0%
Distinct species in reports 2
Distinct breeds in reports 2
Distinct reactions reported 13
Active ingredients on file 1

Source: FDA Center for Veterinary Medicine — Adverse Event Reporting (CVM AER). Counts reflect voluntary reports only.

Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) Adverse Event Insights

The FDA Center for Veterinary Medicine database currently holds 89 adverse event reports referencing Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage), including 87 reports in which the animal died — a 9780.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage). Reported administration route is Unknown. These numbers reflect voluntary submissions from pet owners, veterinarians, and manufacturers and therefore under-represent mild events and over-represent severe ones — a pattern the FDA has documented repeatedly for pharmacovigilance datasets.

The species most frequently named in Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) reports are Fish (88 reports), Unknown (1 reports), with Fish accounting for the largest share. Within those species, Atlantic Salmon (Salmo salar) (88), Unknown (1) appear most often — though breed popularity and ownership density shape these counts as much as any drug-specific sensitivity. This distribution matters because the same active ingredient can behave very differently across body sizes, ages, and species physiology.

The most commonly reported clinical signs associated with Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) are Death (63), IGA Animal mortality greater than expected (35), Fish body deformity (28), Moribund (24). Of the 106 reports with a coded outcome, Died is the leading category at 59.4%. Because FDA adverse event data describes correlation rather than causation, these figures are best used to frame informed questions with a veterinarian and to compare reporting patterns across related products — not as a standalone safety verdict on Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage).

Source: FDA Center for Veterinary Medicine — Adverse Event Reports FDA Center for Veterinary Medicine — Adverse Event Reports Data reflects voluntary submissions and may not represent actual incidence rates

Related

Data sourced from official AKC, AVMA, ACVO, and breed-club veterinary references. See our methodology for details. Retrieved and formatted by PlainBreed Editorial