Does SODIUM PERBORATE Cause Condition aggravated? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Condition aggravated have been filed in association with SODIUM PERBORATE (Amosan Oral Wound Cleanser Mint). This represents 100.0% of all adverse event reports for SODIUM PERBORATE.
49
Reports of Condition aggravated with SODIUM PERBORATE
100.0%
of all SODIUM PERBORATE reports
7
Deaths
49
Hospitalizations
How Dangerous Is Condition aggravated From SODIUM PERBORATE?
Of the 49 reports, 7 (14.3%) resulted in death, 49 (100.0%) required hospitalization, and 7 (14.3%) 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 SODIUM PERBORATE. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does SODIUM PERBORATE Cause?
Therapy non-responder (49)
Arthralgia (48)
Arthropathy (48)
Drug hypersensitivity (48)
Drug ineffective (48)
Drug intolerance (48)
Gastrointestinal toxicity (48)
Hepatotoxicity (48)
Infection (48)
Joint injury (48)
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)