Caduet (Amlodipine/Atorvastatin )
62 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.
62
Total Reports
23
Deaths Reported
3710.0%
Death Rate
Active Ingredients
Caduet (Amlodipine/Atorvastatin )
Administration Routes
UnknownOralOther
Species Affected
Cat 31
Dog 30
Unknown 1
Most Affected Breeds
Domestic Shorthair 25
Retriever - Labrador 6
Poodle (unspecified) 3
Spaniel (unspecified) 2
Maltese 2
Shih Tzu 2
Terrier - Jack Russell 1
Unknown 1
Bichon Frise 1
Cat (unknown) 1
Most Reported Reactions
Lethargy (see also Central nervous system depression in 'Neurological') 21
Death by euthanasia 17
Anorexia 14
Elevated blood urea nitrogen (BUN) 13
Vomiting 11
Other abnormal test result NOS 10
Diarrhoea 9
Anaemia NOS 9
Hypertension 8
Elevated creatinine 8
Leucocytosis NOS 8
Seizure NOS 7
Outcome Breakdown
Ongoing
23 (37.7%)
Euthanized
17 (27.9%)
Recovered/Normal
8 (13.1%)
Outcome Unknown
7 (11.5%)
Died
6 (9.8%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.