Altren® — veterinary medication

Overview

Source: Animal Drugs @ FDA

Proprietary name

Altren®

Active ingredient

Altrenogest

Application type

ANADA

Sponsor

Aurora Pharmaceutical, Inc.

Applications on record

1

First published

August 1, 2017

Adverse event reports

Source: openFDA VeDDRA

228

Reports mentioning this ingredient

May 27, 1987 – January 21, 2026

2

Classified serious

per reporter assessment

10

Lack of expected efficacy

resistance signal

75

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 “ALTRENOGEST”. 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
Unclassifiable adverse event	136
Accidental exposure	75
Disorders of menstrual cycle NOS	43
Abdominal pain	23
Headache	16
Containers, Leaking	16
INEFFECTIVE, ESTRUS SUPPRESSIO	14
No sign	11
Vials, Leaking	10
Rash	8
Nausea	8
Female reproductive tract disorder NOS	8
Caps, Abnormal	8
Lack of efficacy - NOS	6
Abortion	5
Vomiting	5
Fever	5
INEFFECTIVE, ESTRUS SYNCHRONIZ	5
Pruritus	5
Injection site pain	5

Species affected

Source: openFDA VeDDRA

Human 112 Horse 53 Pig 12 Dog 6 Other 1

Regulatory context

Abbreviated New Animal Drug Application (ANADA). A generic animal drug demonstrating bioequivalence, pharmaceutical equivalence and identical manufacturing criteria to the pioneer application. Veterinary generics have no formal therapeutic-equivalence coding system; they match the pioneer NADA specification instead.

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