Elkhound - Norwegian Grey — FDA Adverse Event Profile

Elkhound - Norwegian Grey Pet Health Insights

Across the FDA Center for Veterinary Medicine adverse event database, Elkhound - Norwegian Grey accounts for 86 submitted reports and currently ranks #240 by report volume within the dog population. Of those reports, 3 involved a death outcome — a 350.0% case-fatality figure calculated directly from the underlying FDA records rather than from external mortality studies. The mean age at time of reporting is 5.4 years, with an average recorded body weight of 23.4 kg (51.6 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 Elkhound - Norwegian Grey are Vomiting (12 reports), Lack of efficacy (bacteria) - Borrelia (8 reports), Seizure NOS (6 reports), together capturing a substantial share of the top-reaction traffic seen in this breed's record. On the product side, Pyrantel Pamoate;Sarolaner appears in 27 reports and is the single most-referenced drug, followed by Moxidectin (13) and Sarolaner (10). Counts like these surface which therapeutic classes dominate the reporting stream — useful context when comparing reactions across breeds of the same dog species.

Outcome coding on the 86 reports with a recorded status is dominated by Ongoing (59.3% of coded outcomes). Annual submission volume ranges from 2,012 to 2,025 reports across the 13 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 dog.