Drug profile

The FDA adverse-event record for Estriol Tablets

1,320 FDA reports name Estriol Tablets, a high-volume drug in the CVM extract. Species, reactions, and outcomes follow.

#150 of 2,679
by report volume (all drugs)
1,320
adverse-event reports
6.4%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Estriol Tablets ranks #150 of 2679 by total reports (1,320) and #721 of 1130 by death-coded share (6.4%). National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#150
This drug, reports of 2679
#721
This drug, death share of 1130

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Estriol Tablets has 1,320 reports now versus 1,305 in that prior snapshot: 15 more (1.1%).

Report change
+15
Death-coded reports
+0
Death-coded share
−0.1 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Estriol Tablets changes

Signature read: 1,320 reports place Estriol Tablets in the upper third of FDA AER volume (#150 of 2,679).

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
1,320
Total Reports
85
Deaths Reported
6.4%
Death-coded share of reports

Active Ingredients

Estriol Tablets

Administration Routes

OralUnknownTopicalOther

Species Affected

Dog 1,291
Unknown 21
Human 6
Cat 2

Most Affected Breeds

Crossbred Canine/dog 286
Retriever - Labrador 73
Doberman Pinscher 62
Terrier - Yorkshire 50
Shepherd Dog - German 49
Dog (unknown) 36
Poodle - Miniature 34
Unknown 30
Boxer (German Boxer) 26
Terrier (unspecified) 26

Most Reported Reactions

Lack of efficacy - NOS 401
Swollen vulva 336
Vaginal discharge 75
Death by euthanasia 75
Urinary incontinence 69
Genital tract licking 67
Lethargy (see also Central nervous system depression in 'Neurological') 62
Decreased appetite 60
Vaginal haemorrhage 57
Emesis (multiple) 54
Weight loss 52
Anorexia 50

Outcome Breakdown

Ongoing
777 (59.7%)
Recovered/Normal
225 (17.3%)
Outcome Unknown
185 (14.2%)
Euthanized
74 (5.7%)
Recovered with Sequela
29 (2.2%)
Died
11 (0.8%)

Estriol Tablets: high report volume in the FDA AER row

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.

High-volume nationwide drug peers

Two openFDA-derived peer sets for Estriol Tablets, both floored at ≥50 reports so the neighborhoods stay in the advertised mass.

What to do with this drug

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Estriol Tablets (#150 of 2,679 by report volume); death-coded 6.4%. PlainBreed drug row · report volume stamp 1,320 · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →