Praziquantel; Moxidectin
169 adverse event reports submitted to the FDA
Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
169
Total Reports
13
Deaths Reported
770.0%
Death Rate
Active Ingredients
Praziquantel; Moxidectin
Administration Routes
OralUnknownTopicalIntraocular
Species Affected
Horse 115
Unknown 35
Dog 15
Human 2
Fish 1
Cat 1
Most Affected Breeds
Unknown 37
Quarter Horse 30
Horse (unknown) 26
Thoroughbred 14
Paint 8
Arab 6
Tennessee Walking Horse 5
Crossbred Equine/horse 3
Mustang 3
Miniature 2
Most Reported Reactions
Colic 25
Lack of efficacy - NOS 18
Ataxia 13
Lethargy (see also Central nervous system depression in 'Neurological') 12
No sign 12
Product syringe issue 11
Fever 11
Difficulty of Use 11
Depression 8
Death by euthanasia 8
INEFFECTIVE, PINWORMS 7
Behavioural disorder NOS 7
Outcome Breakdown
Recovered/Normal
57 (42.5%)
Outcome Unknown
38 (28.4%)
Ongoing
24 (17.9%)
Euthanized
7 (5.2%)
Died
6 (4.5%)
Recovered with Sequela
2 (1.5%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.