Reaction profile

The FDA adverse-event record for product syringe missing

498 FDA reports name product syringe missing, a high-volume reaction in the CVM extract (VeDDRA 99861). Plate stamps and neighbourhood peers follow.

#647 of 2,481
by report volume (all reactions)
498
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. Product syringe missing has 498 reports now versus 492 in that prior snapshot: 6 more (1.2%).

Report change
+6
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 Product syringe missing changes

FDA AER · VeDDRA plate

Code 99861 VOL-LOW

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

  • VOL-LOW 498 reports
  • DEATH-RARE 0.0%
  • MID-PACK #647/2481
  • PHOTO-FINISH Bloated
  • SPECIES-UNKNOWN Unknown · 496
  • DRUG-LEAD Meloxicam · 263
  • DESK-NARROW 2 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Bloated (±1 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 Product syringe missing

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

Vomiting · highest174348Application site stic… · near502Pancreas disorder · near501Blepharospasm · near500Product syringe missi… · thi…498Bloated · near497Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Product syringe missing

Product syringe missing: low death-coded share in the FDA AER plate

Signature read: Product syringe missing's 0.0% death-coded share is among the lowest in the openFDA reaction corpus. Report volume is upper-third scale: 498 named reports in the openFDA extract. Death-coded share is lower-third: 0 of 498 reports (0.0% of named reports). Nearest volume peer: Bloated (±1 reports). Lead species Unknown (496). Lead co-reported drug Meloxicam (263).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Meloxicam 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 496
Dog 1
Human 1

Breeds Most Affected

Unknown 497
Pit Bull 1

Associated Drugs

Meloxicam 263
Cyclosporine 79
Capromorelin Tartrate 32
Cyclosporine A 29
Orbifloxacin Oral Suspension 20
Omeprazole 12
Metronidazole 11
Capromorelin 10
Pradofloxacin 9
Ponazuril 9
Omeprazole 37% Oral Paste 4
Itraconazole 4
Doxycycline Hyclate 3
Eprinomectin + Esafoxolaner + Praziquantel 2
Amoxicillin Trihydrate, Potassium Clavulanate 2
Methimazole 2
Deslorelin 1
Dirlotapide 1
Pyrantel 1
Sometribove 1

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Product syringe 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 (498 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 Product syringe missing (#647 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 →