PROBENECID
Generic: PROBENECID
Lannett CompanyManufacturer
ORALRoute
PROBENECIDActive Substance
1976-07-29Original Approval
PROBENECID is FDA application ANDA080966, sponsored by LANNETT. 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.
Top Reported Reactions
1
DIARRHOEA
105 reports
2
DRUG INEFFECTIVE
69 reports
3
OFF LABEL USE
63 reports
4
DYSPNOEA
53 reports
5
NAUSEA
50 reports
6
VOMITING
49 reports
7
ACUTE KIDNEY INJURY
48 reports
8
ASTHENIA
48 reports
9
ADENOVIRUS INFECTION
47 reports
10
FATIGUE
47 reports