Does BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE Cause Condition aggravated? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Condition aggravated have been filed in association with BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE. This represents 77.6% of all adverse event reports for BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE.
How Dangerous Is Condition aggravated From BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE?
Of the 38 reports, 38 (100.0%) resulted in death, 29 (76.3%) required hospitalization, and 26 (68.4%) 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 SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE. However, 38 reports have been filed with the FAERS database.