Does BEZAFIBRATE Cause Hepatic function abnormal? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Hepatic function abnormal have been filed in association with BEZAFIBRATE. This represents 2.0% of all adverse event reports for BEZAFIBRATE.
6
Reports of Hepatic function abnormal with BEZAFIBRATE
2.0%
of all BEZAFIBRATE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Hepatic function abnormal From BEZAFIBRATE?
Of the 6 reports, 4 (66.7%) required hospitalization, and 2 (33.3%) 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 BEZAFIBRATE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does BEZAFIBRATE Cause?
Myalgia (29)
Abdominal pain (25)
Rhabdomyolysis (21)
Back pain (20)
Blood creatine phosphokinase increased (19)
Acute myocardial infarction (17)
Pancreatitis acute (17)
Pyrexia (16)
Acute coronary syndrome (15)
Drug intolerance (15)
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 BEZAFIBRATE Alternatives Have Lower Hepatic function abnormal Risk?
BEZAFIBRATE vs BEZLOTOXUMAB
BEZAFIBRATE vs BGB-11417
BEZAFIBRATE vs BICALUTAMIDE
BEZAFIBRATE vs BICTEGRAVIR
BEZAFIBRATE vs BICTEGRAVIR\EMTRICITABINE\TENOFOVIR ALAFENAMIDE