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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 Hyperbilirubinaemia? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Hyperbilirubinaemia have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.0% of all adverse event reports for DULOXETINE.

15
Reports of Hyperbilirubinaemia with DULOXETINE
0.0%
of all DULOXETINE reports
0
Deaths
3
Hospitalizations

How Dangerous Is Hyperbilirubinaemia From DULOXETINE?

Of the 15 reports, 3 (20.0%) required hospitalization.

Is Hyperbilirubinaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 15 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 Hyperbilirubinaemia?

METHOTREXATE (603) RIBAVIRIN (560) VINCRISTINE (479) CYTARABINE (397) PEGASPARGASE (349) ACETAMINOPHEN (330) CYCLOPHOSPHAMIDE (330) DEXAMETHASONE (315) CAPECITABINE (279) SOFOSBUVIR (260)

Which DULOXETINE Alternatives Have Lower Hyperbilirubinaemia Risk?

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

Related Pages

DULOXETINE Full Profile All Hyperbilirubinaemia Reports All Drugs Causing Hyperbilirubinaemia DULOXETINE Demographics