Clinacox® and Stafac® — veterinary medication

Overview

Source: Animal Drugs @ FDA

Proprietary name

Clinacox® and Stafac®

Active ingredient

Diclazuril Virginiamycin

Application type

NADA

Sponsor

Elanco US Inc.

Applications on record

1

First published

July 17, 2020

Adverse event reports

Source: openFDA VeDDRA

129

Reports mentioning this ingredient

March 27, 2014 – December 22, 2025

52

Classified serious

per reporter assessment

34

Lack of expected efficacy

resistance signal

2

Human operator exposure

needle-stick or splash

Not a risk measure. Veterinary adverse event reports are influenced by how many animals are treated, reporting practice and product age. Reports do not establish that the product caused the event, and a single report can cover an entire herd or flock. Attribution here is by active ingredient because the source dataset redacts brand names.

Attributed by active ingredient “DICLAZURIL ORAL PELLETS”. Green Book ingredient names and VeDDRA ingredient names do not always agree exactly, so attribution is approximate and labelled as such.

Reported reactions

Source: openFDA VeDDRA

Clinical signs coded in the VICH VeDDRA four-level hierarchy, most frequent first.

Reaction terms reported for this ingredient, by report count.
Reaction (VeDDRA term)	Reports	Relative frequency
Lack of efficacy (protozoa) - NOS	29
Containers, Damaged	17
Closure, Abnormal	14
Underfilling, Container	13
Defect Unknown/Not Specified	10
Underfilling, Buckets/Pails	8
Containers, Abnormal	8
Uncoded sign	6
Drug administration duration too long	6
Weight loss	5
Death by euthanasia	5
Product Defect, General	4
Recumbency	4
Diarrhoea	4
Colic	4
Product defect, product difficult to use/handle (see also 'Drug device difficult to use/handle')	4
UNPALATABLE	3
Lack of efficacy - NOS	3
Lack of efficacy (endoparasite) - NOS	3
Underdose	3

Species affected

Source: openFDA VeDDRA

Horse 66 Other Equids 1 Other Mammals 1 Dog 1

Regulatory context

New Animal Drug Application (NADA). A pioneer approval evaluated for target animal safety, therapeutic effectiveness, manufacturing controls and — for food-producing species — human food safety including residue depletion.

Extra-label use in food-producing animals is governed by the Animal Medicinal Drug Use Clarification Act of 1994 (AMDUCA) and 21 CFR Part 530. It requires a valid veterinarian-client-patient relationship and is prohibited outright for certain drug classes. Withdrawal times are determined by FARAD, not by this index.

Sources for this page

Animal Drugs @ FDA	FDA CVM	Applications, sponsor, status, withdrawal
Animal & Veterinary Events	FDA CVM	VeDDRA adverse event aggregates by active ingredient