Does ETRUMADENANT Cause Febrile neutropenia? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Febrile neutropenia have been filed in association with ETRUMADENANT. This represents 22.9% of all adverse event reports for ETRUMADENANT.
16
Reports of Febrile neutropenia with ETRUMADENANT
22.9%
of all ETRUMADENANT reports
9
Deaths
15
Hospitalizations
How Dangerous Is Febrile neutropenia From ETRUMADENANT?
Of the 16 reports, 9 (56.3%) resulted in death, 15 (93.8%) required hospitalization, and 7 (43.8%) were considered life-threatening.
Is Febrile neutropenia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETRUMADENANT. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does ETRUMADENANT Cause?
Disease progression (19)
Platelet count decreased (15)
Pyrexia (14)
Hyponatraemia (12)
Drug hypersensitivity (11)
Vomiting (11)
Diarrhoea (10)
Nausea (10)
Acute kidney injury (7)
Fungal infection (7)
What Other Drugs Cause Febrile neutropenia?
CYCLOPHOSPHAMIDE (11,318)
DOXORUBICIN (8,844)
VINCRISTINE (8,676)
RITUXIMAB (6,382)
CYTARABINE (6,142)
METHOTREXATE (6,091)
ETOPOSIDE (5,966)
CARBOPLATIN (4,888)
DEXAMETHASONE (4,382)
PREDNISONE (3,956)