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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PROBENECID Cause Condition aggravated? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with PROBENECID (Probenecid). This represents 5.3% of all adverse event reports for PROBENECID.

5
Reports of Condition aggravated with PROBENECID
5.3%
of all PROBENECID reports
1
Deaths
1
Hospitalizations

How Dangerous Is Condition aggravated From PROBENECID?

Of the 5 reports, 1 (20.0%) resulted in death, 1 (20.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PROBENECID. However, 5 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Related Pages

PROBENECID Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated PROBENECID Demographics