Amoxicillin, Clavulanate Potassium

68 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.
68
Total Reports
2
Deaths Reported
290.0%
Death Rate

Active Ingredients

Amoxicillin, Clavulanate Potassium

Administration Routes

UnknownOral

Species Affected

Unknown 37
Dog 15
Cat 14
Human 2

Most Affected Breeds

Unknown 39
Domestic Shorthair 12
Retriever - Labrador 3
Boxer (German Boxer) 2
Cat (unknown) 2
Dog (unknown) 2
Chihuahua 2
Poodle - Toy 1
Dachshund (unspecified) 1
Poodle (unspecified) 1

Most Reported Reactions

Color, Abnormal 19
Vomiting 13
Underfilling, Package 9
Appearance, Abnormal 7
Suspension, Abnormal 6
Seal, Abnormal 5
Diarrhoea 4
Tablets, Abnormal 4
Lack of efficacy - NOS 3
Loose stool 3
Abnormal posture NOS 3
Excessive chewing, licking and/or grooming 3

Outcome Breakdown

Outcome Unknown
20 (64.5%)
Recovered/Normal
5 (16.1%)
Ongoing
4 (12.9%)
Died
2 (6.5%)

Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.