Does BISMUTH SUBNITRATE Cause Intentional product misuse? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Intentional product misuse have been filed in association with BISMUTH SUBNITRATE (Bismuthum Subnitricum). This represents 58.0% of all adverse event reports for BISMUTH SUBNITRATE.
47
Reports of Intentional product misuse with BISMUTH SUBNITRATE
58.0%
of all BISMUTH SUBNITRATE reports
47
Deaths
44
Hospitalizations
How Dangerous Is Intentional product misuse From BISMUTH SUBNITRATE?
Of the 47 reports, 47 (100.0%) resulted in death, 44 (93.6%) required hospitalization, and 43 (91.5%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISMUTH SUBNITRATE. However, 47 reports have been filed with the FAERS database.
What Other Side Effects Does BISMUTH SUBNITRATE Cause?
Off label use (61)
Hyponatraemia (59)
Stress (59)
Multiple organ dysfunction syndrome (58)
Condition aggravated (57)
General physical health deterioration (57)
Myasthenia gravis (57)
Sepsis (57)
Somnolence (57)
Abdominal distension (51)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)