Does BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE Cause Hyperphosphataemia? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Hyperphosphataemia have been filed in association with BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE. This represents 49.0% of all adverse event reports for BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE.
How Dangerous Is Hyperphosphataemia From BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE?
Of the 24 reports, 24 (100.0%) resulted in death, 24 (100.0%) required hospitalization, and 23 (95.8%) were considered life-threatening.
Is Hyperphosphataemia 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, 24 reports have been filed with the FAERS database.