Does BISMUTH SUBNITRATE Cause Condition aggravated? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Condition aggravated have been filed in association with BISMUTH SUBNITRATE (Bismuthum Subnitricum). This represents 70.4% of all adverse event reports for BISMUTH SUBNITRATE.
57
Reports of Condition aggravated with BISMUTH SUBNITRATE
70.4%
of all BISMUTH SUBNITRATE reports
57
Deaths
51
Hospitalizations
How Dangerous Is Condition aggravated From BISMUTH SUBNITRATE?
Of the 57 reports, 57 (100.0%) resulted in death, 51 (89.5%) required hospitalization, and 42 (73.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISMUTH SUBNITRATE. However, 57 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)
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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)