Does SODIUM PERBORATE Cause Bone density decreased? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Bone density decreased have been filed in association with SODIUM PERBORATE (Amosan Oral Wound Cleanser Mint). This represents 18.4% of all adverse event reports for SODIUM PERBORATE.
9
Reports of Bone density decreased with SODIUM PERBORATE
18.4%
of all SODIUM PERBORATE reports
6
Deaths
9
Hospitalizations
How Dangerous Is Bone density decreased From SODIUM PERBORATE?
Of the 9 reports, 6 (66.7%) resulted in death, 9 (100.0%) required hospitalization, and 6 (66.7%) were considered life-threatening.
Is Bone density decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM PERBORATE. However, 9 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 Bone density decreased?
EMTRICITABINE\TENOFOVIR DISOPROXIL (16,315)
TENOFOVIR DISOPROXIL (10,586)
EFAVIRENZ\EMTRICITABINE\TENOFOVIR DISOPROXIL (9,547)
COBICISTAT\ELVITEGRAVIR\EMTRICITABINE\TENOFOVIR DISOPROXIL (4,529)
EMTRICITABINE\RILPIVIRINE\TENOFOVIR DISOPROXIL (3,497)
TERIPARATIDE (1,178)
DENOSUMAB (968)
METHOTREXATE (599)
ADALIMUMAB (584)
TOCILIZUMAB (573)