Furosemide Tablets

51 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.

Total Reports

Deaths Reported

780.0%

Death Rate

Active Ingredients

Furosemide Tablets

Administration Routes

UnknownOral

Species Affected

Unknown 31

Dog 19

Cat 1

Most Affected Breeds

Unknown 31

Chihuahua 4

Terrier - Yorkshire 4

Crossbred Canine/dog 2

Spitz - German Pomeranian 1

Terrier (unspecified) 1

Retriever - Labrador 1

Chin 1

Crossbred Feline/cat 1

Coton de Tuléar 1

Most Reported Reactions

Uncoded sign 15

Lot # and /or Expiration date missing 9

Lot # and/or Expiration date illegible 6

Physical product label issues 5

Lethargy (see also Central nervous system depression in 'Neurological') 4

Behavioural disorder NOS 4

Product label issues 4

Tablets, Abnormal 4

Polydipsia 4

Polyuria 4

Vomiting 3

Medication error 3

Outcome Breakdown

Outcome Unknown

5 (25.0%)

Recovered/Normal

5 (25.0%)

Ongoing

4 (20.0%)

Euthanized

3 (15.0%)

Recovered with Sequela

2 (10.0%)

Died

1 (5.0%)

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