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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 PAROXETINE Cause Hyperbilirubinaemia? 38 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Hyperbilirubinaemia have been filed in association with PAROXETINE (Paroxetine). This represents 0.2% of all adverse event reports for PAROXETINE.

38
Reports of Hyperbilirubinaemia with PAROXETINE
0.2%
of all PAROXETINE reports
6
Deaths
33
Hospitalizations

How Dangerous Is Hyperbilirubinaemia From PAROXETINE?

Of the 38 reports, 6 (15.8%) resulted in death, 33 (86.8%) required hospitalization, and 1 (2.6%) were considered life-threatening.

Is Hyperbilirubinaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 38 reports have been filed with the FAERS database.

What Other Side Effects Does PAROXETINE Cause?

Foetal exposure during pregnancy (1,894) Drug ineffective (1,457) Toxicity to various agents (1,407) Drug abuse (1,214) Anxiety (1,201) Nausea (1,063) Suicidal ideation (999) Drug interaction (991) Confusional state (975) Dizziness (937)

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 PAROXETINE Alternatives Have Lower Hyperbilirubinaemia Risk?

PAROXETINE vs PAROXETINE\PAROXETINE PAROXETINE vs PAROXETINE\PAROXETINE ANHYDROUS PAROXETINE vs PASIREOTIDE PAROXETINE vs PASIREOTIDE DIASPARTATE PAROXETINE vs PATIROMER

Related Pages

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