Reaction profile

The FDA adverse-event record for lot # and /or expiration date missing

505 FDA adverse-event reports reference lot # and /or expiration date missing (VeDDRA 99843). See the species, breeds, and drugs most associated with it below.

505
reports citing this reaction
0.4%
death-coded share
Unknown
most-affected species
Ivermectin + Pyrantel As Pamoate Salt
most-associated drug
Verify with FDA CVM →
505
Total Reports
2
Deaths
0.4%
Death Rate

Species Most Affected

Unknown 473
Dog 18
Cat 9
Human 3
Chicken 1
Goat 1

Breeds Most Affected

Unknown 476
Domestic Shorthair 5
Cat (unknown) 3
Pit Bull 2
Terrier - Cairn 1
Poodle - Toy 1
Wyandotte 1
Siberian Husky 1
Collie - Border 1
Shepherd Dog - Australian 1

Associated Drugs

Ivermectin + Pyrantel As Pamoate Salt 31
Ivermectin/Pyrantel Pamoate Chewable 68Mcg/163Mg 21
Nitenpyram 18
Moxidectin 16
Phenylpropanolamine Hcl 15
Recombinant Human Insulin 15
Dexamethasone Sodium Phosphate 15
Ivermectin/Pyrantel Pamoate Chewable 272Mcg/652Mg 13
Ceftiofur 13
Carprofen 12
Firocoxib 57 Mg Chewable 11
Milbemycin Oxime + Spinosad 9
Furosemide Tablets 9
Ivermectin, Pyrantel 9
Orbifloxacin Tablets 9
Firocoxib 227 Mg 8
Insulin Human 8
Fenbendazol Suspension 8
Firocoxib 227 Mg Chewable 7
Afoxolaner 7

Lot # and /or Expiration date missing Reaction Insights

505 reports name Lot # and /or Expiration date missing; 2 recorded a death outcome (0.4% of reported events, not a population-level mortality rate). VeDDRA code: 99843.

By species: Unknown (473 reports), Dog (18 reports), Cat (9 reports). By breed: Unknown (476), Domestic Shorthair (5), Cat (unknown) (3).

Most co-reported drugs: Ivermectin + Pyrantel As Pamoate Salt (31 reports), Ivermectin/Pyrantel Pamoate Chewable 68Mcg/163Mg (21 reports), Nitenpyram (18 reports), Moxidectin (16 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.