Does DUTASTERIDE Cause Hepatic function abnormal? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Hepatic function abnormal have been filed in association with DUTASTERIDE (Dutasteride). This represents 0.6% of all adverse event reports for DUTASTERIDE.
24
Reports of Hepatic function abnormal with DUTASTERIDE
0.6%
of all DUTASTERIDE reports
2
Deaths
15
Hospitalizations
How Dangerous Is Hepatic function abnormal From DUTASTERIDE?
Of the 24 reports, 2 (8.3%) resulted in death, 15 (62.5%) required hospitalization, and 1 (4.2%) 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 DUTASTERIDE. However, 24 reports have been filed with the FAERS database.
What Other Side Effects Does DUTASTERIDE Cause?
Dyspnoea (502)
Asthma (329)
Wheezing (329)
Malaise (311)
Condition aggravated (300)
Sleep disorder due to a general medical condition (290)
Dizziness (288)
Fall (280)
Insomnia (276)
Fatigue (273)
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 DUTASTERIDE Alternatives Have Lower Hepatic function abnormal Risk?
DUTASTERIDE vs DUTASTERIDE\TAMSULOSIN
DUTASTERIDE vs DUVELISIB
DUTASTERIDE vs DYDROGESTERONE
DUTASTERIDE vs EBASTINE
DUTASTERIDE vs ECALLANTIDE