Reaction profile
The FDA adverse-event record for drug dose administration interval too long
3,246 FDA adverse-event reports reference drug dose administration interval too long (VeDDRA 99823). See the species, breeds, and drugs most associated with it below.
- 3,246
- reports citing this reaction
- 1.3%
- death-coded share
- Dog
- most-affected species
- Ivermectin + Pyrantel As Pamoate Salt
- most-associated drug
Species Most Affected
Breeds Most Affected
Associated Drugs
Drug dose administration interval too long Reaction Insights
3,246 reports name Drug dose administration interval too long; 42 recorded a death outcome (1.3% of reported events, not a population-level mortality rate). VeDDRA code: 99823.
By species: Dog (2,918 reports), Cat (188 reports), Cattle (131 reports). By breed: Retriever - Labrador (444), Crossbred Canine/dog (270), Retriever - Golden (151).
Most co-reported drugs: Ivermectin + Pyrantel As Pamoate Salt (610 reports), Moxidectin (505 reports), Fluralaner Chew Tablets (381 reports), Milbemycin Oxime + Spinosad (321 reports).
Read these counts as reporting volume, not risk: per our methodology, co-reporting reflects temporal association captured in voluntary submissions, not proof that a drug caused this reaction. A widely-prescribed drug will rack up more raw co-reports at an identical true rate than a rarely-used one, so compare within similar-exposure products.
Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025
Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.