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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 cirrhosis? 94 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 94 reports of Hepatic cirrhosis have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.2% of all adverse event reports for DULOXETINE.

94
Reports of Hepatic cirrhosis with DULOXETINE
0.2%
of all DULOXETINE reports
34
Deaths
20
Hospitalizations

How Dangerous Is Hepatic cirrhosis From DULOXETINE?

Of the 94 reports, 34 (36.2%) resulted in death, 20 (21.3%) required hospitalization.

Is Hepatic cirrhosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 94 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 cirrhosis?

ADALIMUMAB (1,760) METHOTREXATE (1,650) ETANERCEPT (931) TOCILIZUMAB (903) RITUXIMAB (863) INFLIXIMAB (831) ABATACEPT (824) HYDROXYCHLOROQUINE (807) LEFLUNOMIDE (780) SULFASALAZINE (760)

Which DULOXETINE Alternatives Have Lower Hepatic cirrhosis Risk?

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

Related Pages

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