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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 CYTARABINE Cause Hepatic lesion? 40 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Hepatic lesion have been filed in association with CYTARABINE (cytarabine). This represents 0.1% of all adverse event reports for CYTARABINE.

40
Reports of Hepatic lesion with CYTARABINE
0.1%
of all CYTARABINE reports
14
Deaths
13
Hospitalizations

How Dangerous Is Hepatic lesion From CYTARABINE?

Of the 40 reports, 14 (35.0%) resulted in death, 13 (32.5%) required hospitalization, and 4 (10.0%) were considered life-threatening.

Is Hepatic lesion Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CYTARABINE. However, 40 reports have been filed with the FAERS database.

What Other Side Effects Does CYTARABINE Cause?

Febrile neutropenia (6,142) Off label use (4,183) Pyrexia (2,992) Neutropenia (2,558) Disease progression (2,352) Drug ineffective (2,281) Thrombocytopenia (2,148) Sepsis (2,013) Myelosuppression (1,869) Product use in unapproved indication (1,619)

What Other Drugs Cause Hepatic lesion?

OCTREOTIDE (296) EVEROLIMUS (171) RIBOCICLIB (144) LETROZOLE (139) CAPECITABINE (124) ADALIMUMAB (123) METHOTREXATE (108) FULVESTRANT (107) PALBOCICLIB (104) CYCLOPHOSPHAMIDE (101)

Which CYTARABINE Alternatives Have Lower Hepatic lesion Risk?

CYTARABINE vs CYTARABINE\DAUNORUBICIN CYTARABINE vs DABIGATRAN CYTARABINE vs DABIGATRAN ETEXILATE CYTARABINE vs DABRAFENIB CYTARABINE vs DABRAFENIB\TRAMETINIB

Related Pages

CYTARABINE Full Profile All Hepatic lesion Reports All Drugs Causing Hepatic lesion CYTARABINE Demographics