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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DULOXETINE Cause Hepatic failure? 75 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 75 reports of Hepatic failure have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.1% of all adverse event reports for DULOXETINE.

75
Reports of Hepatic failure with DULOXETINE
0.1%
of all DULOXETINE reports
20
Deaths
46
Hospitalizations

How Dangerous Is Hepatic failure From DULOXETINE?

Of the 75 reports, 20 (26.7%) resulted in death, 46 (61.3%) required hospitalization, and 10 (13.3%) were considered life-threatening.

Is Hepatic failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 75 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 failure?

ACETAMINOPHEN (1,392) RIBAVIRIN (888) CYCLOPHOSPHAMIDE (629) METHOTREXATE (598) BEVACIZUMAB (558) SOFOSBUVIR (525) RITUXIMAB (513) VINCRISTINE (468) DOXORUBICIN (462) PREDNISOLONE (425)

Which DULOXETINE Alternatives Have Lower Hepatic failure Risk?

DULOXETINE vs DUPILUMAB DULOXETINE vs DURAGESIC DULOXETINE vs DUROGESIC DULOXETINE vs DUROTEP MT DULOXETINE vs DURVALUMAB

Related Pages

DULOXETINE Full Profile All Hepatic failure Reports All Drugs Causing Hepatic failure DULOXETINE Demographics