Does BISMUTH SUBGALLATE Cause Intentional product misuse? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Intentional product misuse have been filed in association with BISMUTH SUBGALLATE (Devrom). This represents 28.6% of all adverse event reports for BISMUTH SUBGALLATE.
6
Reports of Intentional product misuse with BISMUTH SUBGALLATE
28.6%
of all BISMUTH SUBGALLATE reports
6
Deaths
6
Hospitalizations
How Dangerous Is Intentional product misuse From BISMUTH SUBGALLATE?
Of the 6 reports, 6 (100.0%) resulted in death, 6 (100.0%) required hospitalization, and 6 (100.0%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISMUTH SUBGALLATE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does BISMUTH SUBGALLATE Cause?
Abdominal distension (9)
Vomiting (9)
Blood uric acid increased (8)
Dyspnoea (8)
Product use in unapproved indication (7)
Stress (7)
Abdominal pain (6)
Anaemia (6)
Appendicitis (6)
Appendicolith (6)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)