Does BISMUTH SUBNITRATE Cause Activated partial thromboplastin time prolonged? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Activated partial thromboplastin time prolonged have been filed in association with BISMUTH SUBNITRATE (Bismuthum Subnitricum). This represents 39.5% of all adverse event reports for BISMUTH SUBNITRATE.
32
Reports of Activated partial thromboplastin time prolonged with BISMUTH SUBNITRATE
39.5%
of all BISMUTH SUBNITRATE reports
32
Deaths
30
Hospitalizations
How Dangerous Is Activated partial thromboplastin time prolonged From BISMUTH SUBNITRATE?
Of the 32 reports, 32 (100.0%) resulted in death, 30 (93.8%) required hospitalization, and 30 (93.8%) were considered life-threatening.
Is Activated partial thromboplastin time prolonged Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISMUTH SUBNITRATE. However, 32 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 Activated partial thromboplastin time prolonged?
DABIGATRAN ETEXILATE (264)
HEPARIN (225)
RIVAROXABAN (163)
WARFARIN (146)
ACETAMINOPHEN (119)
ALLOPURINOL (110)
AMIODARONE (99)
METRONIDAZOLE (98)
SIMVASTATIN (94)
DARBEPOETIN ALFA (93)