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active substance

Cephalexin — veterinary medicines

Authorised animal medicines containing Cephalexin across national registers. Regulatory residue limits (MRL) and antimicrobial-resistance surveillance are shown when on record. This is a neutral reference and does not provide dosing or veterinary advice.
Reference information only — not veterinary advice and not a dosing source. Always consult a licensed veterinarian before giving any medicine to an animal.

Target species

Dogs

Authorised products

17 authorised products across national registers.

United States — DailyMed (NLM)

United States — FDA Green Book

Residue limits (MRL)

No residue limits (MRL) are recorded for this substance.

Antimicrobial resistance surveillance

E. coli · Dogs

Cephalexin

NARMS

Resistant: 35.4% · 2406/6803 resistant

Year: 2017–2021

Klebsiella spp · Dogs

Cephalexin

NARMS

Resistant: 25.2% · 54/214 resistant

Year: 2019–2021

S. pseudintermedius · Dogs

Cephalexin

NARMS

Resistant: 0% · 0/22 resistant

Year: 2019–2021

Salmonella · Dogs

Cephalexin

NARMS

Resistant: 30% · 30/100 resistant

Year: 2017–2021

Reported adverse events (openFDA)

Spontaneous adverse-event reports that name Cephalexin, by species — reported counts, not proven reactions.

Dog

2,604 reported events

openFDA

Top reactions: Vomiting (701) · Emesis (368) · Lethargy (see also Central nervous system depression in 'Neurological') (356) · Diarrhoea (214) · Other abnormal test result NOS (207)

Source: openFDA Animal & Veterinary adverse-event reports.

Surveillance reference only — these are spontaneous adverse-event report counts, not proven adverse reactions, not causation and not a measure of any product's risk or safety. Always consult a licensed veterinarian.

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