Loratadine
95 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.
95
Total Reports
12
Deaths Reported
1260.0%
Death Rate
Active Ingredients
Loratadine
Administration Routes
OralUnknown
Species Affected
Dog 82
Cat 7
Human 6
Most Affected Breeds
Retriever - Labrador 10
Retriever - Golden 6
Unknown 6
Shih Tzu 5
Shepherd Dog - German 4
Beagle 4
Sheepdog - Shetland 4
Spaniel - Springer English 3
Spaniel - Cocker American 3
Terrier - Yorkshire 3
Most Reported Reactions
Lethargy (see also Central nervous system depression in 'Neurological') 15
Diarrhoea 15
Vomiting 14
Panting 9
Lack of efficacy - NOS 8
Emesis 7
Death by euthanasia 7
Other abnormal test result NOS 7
Polydipsia 6
Behavioural disorder NOS 5
Elevated blood urea nitrogen (BUN) 5
Elevated creatinine 5
Outcome Breakdown
Recovered/Normal
39 (41.1%)
Outcome Unknown
31 (32.6%)
Ongoing
13 (13.7%)
Euthanized
8 (8.4%)
Died
4 (4.2%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.