Does SITAGLIPTIN Cause Acute hepatic failure? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Acute hepatic failure have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.1% of all adverse event reports for SITAGLIPTIN.
21
Reports of Acute hepatic failure with SITAGLIPTIN
0.1%
of all SITAGLIPTIN reports
19
Deaths
8
Hospitalizations
How Dangerous Is Acute hepatic failure From SITAGLIPTIN?
Of the 21 reports, 19 (90.5%) resulted in death, 8 (38.1%) required hospitalization, and 4 (19.0%) were considered life-threatening.
Is Acute hepatic failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 21 reports have been filed with the FAERS database.