Reaction profile

The FDA adverse-event record for physical label missing

383 FDA reports name physical label missing, a high-volume reaction in the CVM extract (VeDDRA 99849). Plate stamps and neighbourhood peers follow.

#751 of 2,481
by report volume (all reactions)
383
reports citing this reaction
0.0%
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. Physical label missing has 383 reports now versus 381 in that prior snapshot: 2 more (0.5%).

Report change
+2
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 Physical label missing changes

FDA AER · VeDDRA plate

Code 99849 VOL-LOW

VOL-LOW · DEATH-RARE · MID-PACK · PHOTO-FINISH · SPECIES-UNKNOWN · DRUG-LEAD · DESK-NARROW · BOOK-FULL

  • VOL-LOW 383 reports
  • DEATH-RARE 0.0%
  • MID-PACK #751/2481
  • PHOTO-FINISH Disorder of red blood…
  • SPECIES-UNKNOWN Unknown · 382
  • DRUG-LEAD Carprofen · 26
  • DESK-NARROW 2 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Disorder of red blood cell NOS (±0 reports)

Upper-third report volume drives the scale stamps on this plate; death-coded share and co-report peers follow. Not a clinical diagnosis.

High-volume neighbourhood around Physical label missing

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

Vomiting · highest174348Petechiae NOS · near384Disorder of red blood… · near383Physical label missing · thi…383Hair modification NOS · near382Proprioception loss · near382Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Physical label missing

Physical label missing: low death-coded share in the FDA AER plate

Signature read: Physical label missing's 0.0% death-coded share is among the lowest in the openFDA reaction corpus. Report volume is upper-third scale: 383 named reports in the openFDA extract. Death-coded share is lower-third: 0 of 383 reports (0.0% of named reports). Nearest volume peer: Disorder of red blood cell NOS (±0 reports). Lead species Unknown (382). Lead co-reported drug Carprofen (26).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Carprofen 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 382
Dog 1

Breeds Most Affected

Unknown 382
Boxer (German Boxer) 1

Associated Drugs

Carprofen 26
Ivermectin, Pyrantel 25
Enrofloxacin 13
Firocoxib 11
Afoxolaner 10
Ceftiofur 9
Tulathromycin 9
Florfenicol Inj Sol 30% W Pg 8
Nitenpyram 7
Meloxicam 7
Ampicillin Trihydrate 7
Gonadorelindiacetate Tetrahydrate Injection 7
Altrenogest Oily Solution 7
Ceftiofur Hydrochloride 6
Moxidectin 6
Fenbendazol Suspension 6
Phenylpropropanolamine Hcl 6
Gonadorelin Diacetate Tetrahydrate 5
Milbemycin 5
Oclacitinib 5

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Physical label missing, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).

Similar report volume

Nearest other reactions by FDA report count (383 here).

Similar death-coded share

Nearest other reactions by death-coded share (0.0% here), distinct from the volume row.

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 Physical label missing (#751 of 2,481 by report volume); death-coded 0.0%. PlainBreed reaction plate · death-coded share stamp 0.0% · 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 →