Drug profile
The FDA adverse-event record for Recombitek C4 - 13D1.R1
139 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Recombitek C4 - 13D1.R1. See the species affected, top reactions, and outcomes below.
- 139
- adverse-event reports
- 10.1%
- death-coded share
- Dog
- most-reported species
- 44
- Lethargy (see also Central nervous system depression in 'Neurological') - top reaction
Active Ingredients
Administration Routes
Species Affected
Most Affected Breeds
Most Reported Reactions
Outcome Breakdown
Recombitek C4 - 13D1.R1 Adverse Event Insights
139 reports name Recombitek C4 - 13D1.R1; 14 recorded a death outcome (10.1% of reported events, not a population-level mortality rate). Active ingredient: Recombitek C4 - 13D1.R1. Administration routes: Subcutaneous, Unknown, Oral, Intramuscular.
By species: Dog (139 reports). By breed: Retriever - Labrador (13), Crossbred Canine/dog (11), Retriever - Golden (11).
Leading clinical signs: Lethargy (see also Central nervous system depression in 'Neurological') (44), Vomiting (42), Diarrhoea (27), Anorexia (20). Outcome, 141 coded reports: Outcome Unknown leads at 47.5%.
Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.
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.