Does SIMEPREVIR Cause Hepatic function abnormal? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Hepatic function abnormal have been filed in association with SIMEPREVIR. This represents 1.1% of all adverse event reports for SIMEPREVIR.
69
Reports of Hepatic function abnormal with SIMEPREVIR
1.1%
of all SIMEPREVIR reports
4
Deaths
28
Hospitalizations
How Dangerous Is Hepatic function abnormal From SIMEPREVIR?
Of the 69 reports, 4 (5.8%) resulted in death, 28 (40.6%) required hospitalization, and 8 (11.6%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIMEPREVIR. However, 69 reports have been filed with the FAERS database.
What Other Side Effects Does SIMEPREVIR Cause?
Off label use (1,166)
Anaemia (999)
Platelet count decreased (833)
White blood cell count decreased (581)
Hepatitis c (537)
Blood bilirubin increased (467)
Drug ineffective (440)
Pyrexia (429)
Rash (388)
Haemoglobin decreased (385)
What Other Drugs Cause Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which SIMEPREVIR Alternatives Have Lower Hepatic function abnormal Risk?
SIMEPREVIR vs SIMPONI
SIMEPREVIR vs SIMVASTATIN
SIMEPREVIR vs SINGULAIR
SIMEPREVIR vs SINTILIMAB
SIMEPREVIR vs SIPONIMOD