Reaction profile

The FDA adverse-event record for ingredient quality issue nos

24 FDA reports name ingredient quality issue nos, a lower-volume reaction in the CVM extract (VeDDRA 93097). Plate stamps and neighbourhood peers follow.

#2085 of 2,481
by report volume (all reactions)
24
reports citing this reaction
4.2%
death-coded share
Unknown
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. INGREDIENT QUALITY ISSUE NOS has 24 reports now versus 24 in that prior snapshot: 0 the same number of (0.0%).

Report change
+0
Death-coded reports
+0
Death-coded share
−0.0 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 INGREDIENT QUALITY ISSUE NOS changes

FDA AER · VeDDRA plate

Code 93097 VOL-TRACE

VOL-TRACE · DEATH-LOW · LOWER-Q · PHOTO-FINISH · SPECIES-UNKNOWN · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-TRACE 24 reports
  • DEATH-LOW 4.2%
  • LOWER-Q #2085/2481
  • PHOTO-FINISH Acute pancreatitis
  • SPECIES-UNKNOWN Unknown · 15
  • DRUG-LEAD Phenylbutazone · 5
  • DESK-WIDE 9 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Acute pancreatitis (±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 INGREDIENT QUALITY ISSUE NOS

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

Vomiting · highest174348Acute pancreatitis · near24Application site para… · near24Cardiac tamponade · near24Eyelid ptosis - neuro… · near24INGREDIENT QUALITY IS… · thi…24Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around INGREDIENT QUALITY ISSUE NOS

INGREDIENT QUALITY ISSUE NOS: low death-coded share in the FDA AER plate

Signature read: 1 death-coded reports is a thin tail count for INGREDIENT QUALITY ISSUE NOS in the CVM extract. Report volume is lower-third scale: 24 named reports in the openFDA extract. Death-coded share is lower-third: 1 of 24 reports (4.2% of named reports). Nearest volume peer: Acute pancreatitis (±0 reports). Lead species Unknown (15). Lead co-reported drug Phenylbutazone (5).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Phenylbutazone 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

Unknown 15
Dog 8
Cat 1

Breeds Most Affected

Unknown 15
Retriever - Labrador 2
Chihuahua 1
Shih Tzu 1
Shepherd Dog - Australian 1
Boxer (German Boxer) 1
Maltese 1
Dog (unknown) 1
Persian 1

Associated Drugs

Phenylbutazone 5
Ivermectin 4
Milbemycin Oxime + Spinosad 4
Miconazole Nitrate 3
Furosemide 3
Milbemycin Oxime + Praziquantel 3
Betamethasone Valerate + Gentamicin Sulfate 2
Gentamicin Sulfate 2
Chondroitin Sulfate (Bovine) + Dimethyl Sulfone + Glucosamine 1
Clindamycin Hydrochloride 1
Milbemycin Oxime 1
Clorsulon + Ivermectin 1
Cyclosporine 1
Lotilaner,Moxidectin,Praziquantel,Pyrantel Pamoate 1
Sarolaner,Moxidectin,Pyrantel 1
Lotilaner 1
Doxycycline 1
Melarsomine 1
Black Pepper + Cordyceps + Docosahexaenoic Acid + Eicosapentaenoic Acid + Kelp + L-Theanine + Lions Mane + Maitake + Phellinus + Reishi + Shiitake + Tumeric Root + Turkey Tail 1
Spinosad 1

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 INGREDIENT QUALITY ISSUE NOS (#2085 of 2,481 by report volume); death-coded 4.2%. PlainBreed reaction plate · death-coded report count stamp 1 · 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 →