Reaction profile

The FDA adverse-event record for wrong information typed on label

26 FDA reports name wrong information typed on label, a lower-volume reaction in the CVM extract (VeDDRA 99979). Plate stamps and neighbourhood peers follow.

#2065 of 2,481
by report volume (all reactions)
26
reports citing this reaction
3.8%
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. Wrong information typed on label has 26 reports now versus 26 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 Wrong information typed on label changes

FDA AER · VeDDRA plate

Code 99979 VOL-TRACE

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

  • VOL-TRACE 26 reports
  • DEATH-LOW 3.8%
  • LOWER-Q #2065/2481
  • PHOTO-FINISH Cushings disease - pi…
  • SPECIES-UNKNOWN Unknown · 13
  • DRUG-LEAD Maropitant Citrate · 2
  • DESK-WIDE 9 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Cushings disease - pituitary dependent (±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 Wrong information typed on label

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

Vomiting · highest174348Cushings disease - pi… · near26Dermoid cyst · near26Feet shifting · near26Haemorrhagic gastritis · near26Wrong information typ… · thi…26Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Wrong information typed on label

Wrong information typed on label: low death-coded share in the FDA AER plate

Signature read: 1 death-coded reports is a thin tail count for Wrong information typed on label in the CVM extract. Report volume is lower-third scale: 26 named reports in the openFDA extract. Death-coded share is lower-third: 1 of 26 reports (3.8% of named reports). Nearest volume peer: Cushings disease - pituitary dependent (±0 reports). Lead species Unknown (13). Lead co-reported drug Maropitant Citrate (2).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Maropitant Citrate 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 13
Dog 9
Cat 4

Breeds Most Affected

Unknown 14
Crossbred Canine/dog 3
Terrier - Yorkshire 2
Domestic Shorthair 2
Terrier - Scottish 1
Manx 1
Pinscher - Miniature 1
Dog (unknown) 1
American Pit Bull Terrier 1

Associated Drugs

Maropitant Citrate 2
Ivermectin 2
Buprenorphine 2
Cefovecin 1
Maropitant 1
Lasalocid Sodium 1
Hydrocortisone Aceponate/Miconazole Nitrate/Gentamicin Sulfate 1
Amoxicillin As Trihydrate; Clavulanate Potassium ( K-Clavulanate) 1
Oclacitinib Maleate 1
Epsiprantel 1
Prednisolone; Trimeprazine Tartrate 1
Oxytetracycline Anhydrous 1
Spinosad 1
Milbemcyin Oxime, Lufenuron, Praziquantel 1
Ivermectin + Pyrantel 1
Levothyroxine Sodium 1
Fenbendazol Granules 1
Insulin Human 1
Carprofen 1
Capromorelin 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 Wrong information typed on label (#2065 of 2,481 by report volume); death-coded 3.8%. 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 →