Does BISMUTH SUBNITRATE Cause Myasthenia gravis? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Myasthenia gravis 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 Myasthenia gravis with BISMUTH SUBNITRATE
70.4%
of all BISMUTH SUBNITRATE reports
57
Deaths
52
Hospitalizations
How Dangerous Is Myasthenia gravis From BISMUTH SUBNITRATE?
Of the 57 reports, 57 (100.0%) resulted in death, 52 (91.2%) required hospitalization, and 43 (75.4%) were considered life-threatening.
Is Myasthenia gravis 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)
Condition aggravated (57)
General physical health deterioration (57)
Sepsis (57)
Somnolence (57)
Abdominal distension (51)
Incorrect route of product administration (49)
What Other Drugs Cause Myasthenia gravis?
EFGARTIGIMOD ALFA-FCAB (691)
ECULIZUMAB (487)
PEMBROLIZUMAB (469)
NIVOLUMAB (451)
RAVULIZUMAB-CWVZ (338)
PREDNISONE (217)
IPILIMUMAB (201)
PYRIDOSTIGMINE (193)
HUMAN IMMUNOGLOBULIN G (186)
ZILUCOPLAN (184)