Does PROBENECID Cause Product use in unapproved indication? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product use in unapproved indication have been filed in association with PROBENECID (Probenecid). This represents 6.4% of all adverse event reports for PROBENECID.
6
Reports of Product use in unapproved indication with PROBENECID
6.4%
of all PROBENECID reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use in unapproved indication From PROBENECID?
Of the 6 reports.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROBENECID. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does PROBENECID Cause?
Drug ineffective (15)
Off label use (13)
Completed suicide (10)
Diarrhoea (10)
Adenovirus infection (9)
Neoplasm progression (9)
Calcinosis (8)
Drug ineffective for unapproved indication (7)
Acute kidney injury (6)
Drug hypersensitivity (6)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)