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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 BISMUTH SUBNITRATE Cause Drug hypersensitivity? 47 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Drug hypersensitivity 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 Drug hypersensitivity with BISMUTH SUBNITRATE
58.0%
of all BISMUTH SUBNITRATE reports
47
Deaths
44
Hospitalizations

How Dangerous Is Drug hypersensitivity 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 Drug hypersensitivity 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 Drug hypersensitivity?

METHOTREXATE (16,677) ETANERCEPT (12,991) ADALIMUMAB (11,599) MORPHINE (11,095) RITUXIMAB (8,924) LEFLUNOMIDE (8,148) INFLIXIMAB (8,119) TOCILIZUMAB (7,883) ABATACEPT (7,808) CODEINE (7,479)

Related Pages

BISMUTH SUBNITRATE Full Profile All Drug hypersensitivity Reports All Drugs Causing Drug hypersensitivity BISMUTH SUBNITRATE Demographics