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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 Off label use? 61 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Off label use have been filed in association with BISMUTH SUBNITRATE (Bismuthum Subnitricum). This represents 75.3% of all adverse event reports for BISMUTH SUBNITRATE.

61
Reports of Off label use with BISMUTH SUBNITRATE
75.3%
of all BISMUTH SUBNITRATE reports
61
Deaths
53
Hospitalizations

How Dangerous Is Off label use From BISMUTH SUBNITRATE?

Of the 61 reports, 61 (100.0%) resulted in death, 53 (86.9%) required hospitalization, and 44 (72.1%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BISMUTH SUBNITRATE. However, 61 reports have been filed with the FAERS database.

What Other Side Effects Does BISMUTH SUBNITRATE Cause?

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) Incorrect route of product administration (49)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Related Pages

BISMUTH SUBNITRATE Full Profile All Off label use Reports All Drugs Causing Off label use BISMUTH SUBNITRATE Demographics