Reaction profile

The FDA adverse-event record for abnormal number of offspring

47 FDA reports name abnormal number of offspring, a lower-volume reaction in the CVM extract (VeDDRA 1912). Plate stamps and neighbourhood peers follow.

#1766 of 2,481
by report volume (all reactions)
47
reports citing this reaction
12.8%
death-coded share
Dog
most-affected species

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. Abnormal number of offspring has 47 reports now versus 46 in that prior snapshot: 1 more (2.2%).

Report change
+1
Death-coded reports
+0
Death-coded share
−0.3 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 Abnormal number of offspring changes

FDA AER · VeDDRA plate

Code 1912 VOL-TRACE

VOL-TRACE · DEATH-ELEV · MID-PACK · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-TRACE 47 reports
  • DEATH-ELEV 12.8%
  • MID-PACK #1766/2481
  • PHOTO-FINISH ALBUMIN/GLOBULIN RATI…
  • SPECIES-DOG Dog · 26
  • DRUG-LEAD Sometribove · 18
  • DESK-WIDE 17 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: ALBUMIN/GLOBULIN RATIO LO, BLD (±0 reports)

Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.

Lower-volume neighbourhood around Abnormal number of offspring

Lower-third volume poles plus nearest peers, not a full reaction corpus board reprint.

Vomiting · highest174348Abnormal number of of… · thi…47ALBUMIN/GLOBULIN RATI… · near47ANISOCYTOSIS · near47Blood in trachea · near47Exocrine pancreatic i… · near47Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Abnormal number of offspring

What the FDA AER plate says about Abnormal number of offspring

Signature read: 47 reports place Abnormal number of offspring in the lower third of FDA AER volume (#1766 of 2,481). Report volume is lower-third scale: 47 named reports in the openFDA extract. 6 of 47 reports were death-coded (12.8% of named reports, not a population mortality rate). Nearest volume peer: ALBUMIN/GLOBULIN RATIO LO, BLD (±0 reports). Lead species Dog (26). Lead co-reported drug Sometribove (18).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Sometribove appears in filings alongside this reaction; that is association, not causation. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Dog 26
Cattle 19
Pig 2

Breeds Most Affected

Holstein-Friesian also known as Holstein 13
Retriever - Golden 7
Cattle (unknown) 4
Dog (unknown) 4
Terrier - Airedale 3
Shepherd Dog - German 3
Retriever - Labrador 2
Bulldog - French 2
Charolais 1
Cattle (other) 1

Associated Drugs

Sometribove 18
Monensin Sodium 9
Fluralaner Chew Tablets 8
Spinosad 5
Milbemycin Oxime + Spinosad 4
Nitenpyram 3
Fluralaner 13.64% 12-Week Chew 3
Oclacitinib Maleate 2
Enrofloxacin 2
Tylosin 2
Porcine Reproductive And Respiratory Syndrome Virus, Sd11-21 Strain 2
Bordetella Bronchiseptica, Field Strain,Erysipelothrix Rhusiopathiae, Se-9 Strain,Pasteurella Multocida, 169 Strain,Pasteurella Multocida, Type D, Atcc 12948 Strain 2
Iron 2
Penicillin 2
Tulathromycin 2
Flunixin Meglumine 2
Dexamethasone 2
Ceftiofur 2
Lincomycin,Spectinomycin 2
Gentamicin 2

What to do with this reaction

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 Abnormal number of offspring (#1766 of 2,481 by report volume); death-coded 12.8%. PlainBreed reaction plate · report volume stamp 47 · 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 →