Does FENOFIBRATE Cause Hepatic function abnormal? 189 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 189 reports of Hepatic function abnormal have been filed in association with FENOFIBRATE (Fenofibrate). This represents 3.3% of all adverse event reports for FENOFIBRATE.
189
Reports of Hepatic function abnormal with FENOFIBRATE
3.3%
of all FENOFIBRATE reports
9
Deaths
93
Hospitalizations
How Dangerous Is Hepatic function abnormal From FENOFIBRATE?
Of the 189 reports, 9 (4.8%) resulted in death, 93 (49.2%) required hospitalization, and 11 (5.8%) 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 FENOFIBRATE. However, 189 reports have been filed with the FAERS database.
What Other Side Effects Does FENOFIBRATE Cause?
Myalgia (411)
Dyspnoea (373)
Fatigue (365)
Asthenia (356)
Dizziness (356)
Fall (354)
Drug ineffective (326)
Pruritus (325)
Nausea (311)
Diarrhoea (310)
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 FENOFIBRATE Alternatives Have Lower Hepatic function abnormal Risk?
FENOFIBRATE vs FENOFIBRIC ACID
FENOFIBRATE vs FENOTEROL
FENOFIBRATE vs FENOTEROL HYDROBROMIDE
FENOFIBRATE vs FENOTEROL HYDROBROMIDE\IPRATROPIUM
FENOFIBRATE vs FENTANYL