Does BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE Cause Activated partial thromboplastin time prolonged? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Activated partial thromboplastin time prolonged have been filed in association with BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE. This represents 22.5% of all adverse event reports for BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE.
How Dangerous Is Activated partial thromboplastin time prolonged From BISMUTH SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE?
Of the 11 reports, 11 (100.0%) resulted in death, 11 (100.0%) required hospitalization, and 11 (100.0%) 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 SUBGALLATE\BUFEXAMAC\LIDOCAINE\TITANIUM DIOXIDE. However, 11 reports have been filed with the FAERS database.