Does DULOXETINE Cause Hepatic function abnormal? 170 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 170 reports of Hepatic function abnormal have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.3% of all adverse event reports for DULOXETINE.
170
Reports of Hepatic function abnormal with DULOXETINE
0.3%
of all DULOXETINE reports
4
Deaths
31
Hospitalizations
How Dangerous Is Hepatic function abnormal From DULOXETINE?
Of the 170 reports, 4 (2.4%) resulted in death, 31 (18.2%) required hospitalization, and 13 (7.6%) 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 DULOXETINE. However, 170 reports have been filed with the FAERS database.
What Other Side Effects Does DULOXETINE Cause?
Nausea (7,355)
Dizziness (6,983)
Drug withdrawal syndrome (6,503)
Headache (5,541)
Fatigue (5,309)
Insomnia (5,270)
Anxiety (4,973)
Paraesthesia (4,854)
Drug ineffective (4,829)
Hyperhidrosis (4,101)
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 DULOXETINE Alternatives Have Lower Hepatic function abnormal Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB