Reaction profile

The FDA adverse-event record for anaphylactoid reaction

2,262 FDA adverse-event reports reference anaphylactoid reaction (VeDDRA 1113). See the species, breeds, and drugs most associated with it below.

2,262
reports citing this reaction
4.2%
death-coded share
Dog
most-affected species
Moxidectin
most-associated drug
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2,262
Total Reports
96
Deaths
4.2%
Death Rate

Species Most Affected

Dog 1,877
Horse 224
Cat 56
Cattle 56
Pig 31
Human 12
Sheep 2
Donkey 2
Goat 1
Bat 1

Breeds Most Affected

Boxer (German Boxer) 164
Retriever - Labrador 155
Chihuahua 143
Terrier - Bull - American Pit 131
Crossbred Canine/dog 95
Dachshund (unspecified) 87
Horse (unknown) 61
Pit Bull 58
Bulldog 52
Pug 51

Associated Drugs

Moxidectin 1,069
Milbemycin Oxime + Spinosad 191
Canine Adenovirus Type 2, Strain Manhattan, 12-13-76; Canine Distemper Virus, St 181
Rabies Virus, Kv 165
Ivermectin(1.55%)/Praziquantel(7.75%) Paste 126
Bordetella Bronchiseptica, Strain 78-9159, Kb 98
Leptospira Canicola L-15 Strain C-51; Leptospira Grippotyphosa 1550 Lot 10005 St 77
Diphenhydramine Hcl 74
Spinosad 73
Imidacloprid + Moxidectin 71
Bordetella Bronchiseptica 92B 012992-7 Strain Boehringer Ingelheim 62
Ivermectin + Pyrantel As Pamoate Salt 47
Ivermectin, Praziquantel 46
Maropitant Citrate 45
Dexamethasone 42
Pyrantel Pamoate 39
Carprofen 38
Borrelia Burgdorferi Strain Ips 930-34-081596; Borrelia Burgdorferi Strain B-31 34
Milbemycin Oxime, Lufenuron 29
Ivermectin 28

Anaphylactoid reaction Reaction Insights

2,262 reports name Anaphylactoid reaction; 96 recorded a death outcome (4.2% of reported events, not a population-level mortality rate). VeDDRA code: 1113.

By species: Dog (1,877 reports), Horse (224 reports), Cat (56 reports). By breed: Boxer (German Boxer) (164), Retriever - Labrador (155), Chihuahua (143).

Most co-reported drugs: Moxidectin (1,069 reports), Milbemycin Oxime + Spinosad (191 reports), Canine Adenovirus Type 2, Strain Manhattan, 12-13-76; Canine Distemper Virus, St (181 reports), Rabies Virus, Kv (165 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.