Reaction profile

The FDA adverse-event record for product syringe calibration unreadable

288 FDA adverse-event reports reference product syringe calibration unreadable (VeDDRA 99858). See the species, breeds, and drugs most associated with it below.

288
reports citing this reaction
0.0%
death-coded share
Unknown
most-affected species
Meloxicam
most-associated drug
Verify with FDA CVM →
288
Total Reports
0
Deaths
0.0%
Death Rate

Species Most Affected

Unknown 281
Dog 5
Human 1
Cat 1

Breeds Most Affected

Unknown 282
Domestic Shorthair 1
Retriever - Labrador 1
Terrier - Boston 1
Boxer (German Boxer) 1
Schnauzer (unspecified) 1
Terrier - West Highland White 1

Associated Drugs

Meloxicam 127
Cyclosporine 77
Capromorelin 47
Capromorelin Tartrate 12
Molidustat 7
Cyclosporine A 6
Orbifloxacin Oral Suspension 6
Dirlotapide 2
Ear Packing 1
Hyaluronate Sodium 1
Balanced Electrolyte Solution 1
Itraconazole 1
Flunixin Meglumine 1
Flunixin Meglumine Oral Paste 1
Unknown Medication 1
Metronidazole 1
Device: Syringe 1

Product syringe calibration unreadable Reaction Insights

288 reports name Product syringe calibration unreadable; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). VeDDRA code: 99858.

By species: Unknown (281 reports), Dog (5 reports), Human (1 reports). By breed: Unknown (282), Domestic Shorthair (1), Retriever - Labrador (1).

Most co-reported drugs: Meloxicam (127 reports), Cyclosporine (77 reports), Capromorelin (47 reports), Capromorelin Tartrate (12 reports).

Read these counts as reporting volume, not risk: per our methodology, co-reporting reflects temporal association captured in voluntary submissions, not proof that a drug caused this reaction. A widely-prescribed drug will rack up more raw co-reports at an identical true rate than a rarely-used one, so compare within similar-exposure products.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.