Doramectin; Phenol
233 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.
233
Total Reports
97
Deaths Reported
4160.0%
Death Rate
Active Ingredients
Doramectin; Phenol
Administration Routes
SubcutaneousUnknownIntramuscularOralTopicalOther
Species Affected
Cattle 147
Unknown 37
Human 16
Dog 13
Sheep 8
Pig 5
Goat 2
Cat 1
Bison 1
White tailed deer 1
Most Affected Breeds
Cattle (other) 66
Unknown 56
Mixed (Cattle) 52
Aberdeen Angus 16
Sheep (unknown) 5
Holstein-Friesian also known as Holstein 5
Retriever - Labrador 3
Crossbred Bovine/Cattle 2
Crossbred Porcine/Pig 2
Goat (unknown) 2
Most Reported Reactions
Death 64
Lack of efficacy (bacteria) - NOS 44
Lack of efficacy - NOS 42
Uncoded sign 23
Other abnormal test result NOS 16
Abnormal test result 15
Abnormal necropsy finding 12
NT - Abnormal necropsy finding NOS 12
Anaphylactic-type reaction 12
INEFFECTIVE, PARASITE(S) NOS 11
CULTURE/TITER DATA ABNORMAL 11
Precipitate, Sediment 11
Outcome Breakdown
Outcome Unknown
119 (46.1%)
Died
95 (36.8%)
Recovered/Normal
23 (8.9%)
Ongoing
14 (5.4%)
Recovered with Sequela
4 (1.6%)
Euthanized
3 (1.2%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.