Does BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE Cause Abdominal distension? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Abdominal distension have been filed in association with BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE. This represents 87.8% of all adverse event reports for BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE.
How Dangerous Is Abdominal distension From BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE?
Of the 43 reports, 43 (100.0%) resulted in death, 33 (76.7%) required hospitalization, and 30 (69.8%) were considered life-threatening.
Is Abdominal distension Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE. However, 43 reports have been filed with the FAERS database.