AMOXICILLIN AND CLAVULANATE POTASSIUM

Generic: AMOXICILLIN AND CLAVULANATE POTASSIUM

Sandoz IncManufacturer
ORALRoute
AMOXICILLINActive Substance
2010-04-21Original Approval

AMOXICILLIN AND CLAVULANATE POTASSIUM is FDA application ANDA090227, sponsored by SANDOZ. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.

Recalls

Class III2017-04-26
Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in Austria

Subpotent Drug; Clavulanic Acid

Top Reported Reactions

1
DIARRHOEA
353 reports
2
DYSPNOEA
351 reports
3
PYREXIA
258 reports
4
NAUSEA
238 reports
5
DRUG INEFFECTIVE
236 reports
6
FATIGUE
235 reports
7
PNEUMONIA
224 reports
8
PRURITUS
224 reports
9
RASH
219 reports
10
PAIN
213 reports