Does SODIUM PERBORATE Cause Contraindicated product administered? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Contraindicated product administered have been filed in association with SODIUM PERBORATE (Amosan Oral Wound Cleanser Mint). This represents 53.1% of all adverse event reports for SODIUM PERBORATE.
26
Reports of Contraindicated product administered with SODIUM PERBORATE
53.1%
of all SODIUM PERBORATE reports
6
Deaths
26
Hospitalizations
How Dangerous Is Contraindicated product administered From SODIUM PERBORATE?
Of the 26 reports, 6 (23.1%) resulted in death, 26 (100.0%) required hospitalization, and 6 (23.1%) were considered life-threatening.
Is Contraindicated product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM PERBORATE. However, 26 reports have been filed with the FAERS database.
What Other Side Effects Does SODIUM PERBORATE Cause?
Condition aggravated (49)
Therapy non-responder (49)
Arthralgia (48)
Arthropathy (48)
Drug hypersensitivity (48)
Drug ineffective (48)
Drug intolerance (48)
Gastrointestinal toxicity (48)
Hepatotoxicity (48)
Infection (48)
What Other Drugs Cause Contraindicated product administered?
ABATACEPT (13,559)
METHOTREXATE (13,121)
ETANERCEPT (12,062)
TOCILIZUMAB (11,547)
ADALIMUMAB (11,270)
LEFLUNOMIDE (11,206)
HYDROXYCHLOROQUINE (10,557)
RITUXIMAB (10,479)
INFLIXIMAB (9,618)
SULFASALAZINE (8,698)