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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 ETRUMADENANT Cause Disease progression? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Disease progression have been filed in association with ETRUMADENANT. This represents 27.1% of all adverse event reports for ETRUMADENANT.

19
Reports of Disease progression with ETRUMADENANT
27.1%
of all ETRUMADENANT reports
19
Deaths
19
Hospitalizations

How Dangerous Is Disease progression From ETRUMADENANT?

Of the 19 reports, 19 (100.0%) resulted in death, 19 (100.0%) required hospitalization, and 18 (94.7%) were considered life-threatening.

Is Disease progression Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ETRUMADENANT. However, 19 reports have been filed with the FAERS database.

What Other Side Effects Does ETRUMADENANT Cause?

Febrile neutropenia (16) 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 Disease progression?

RITUXIMAB (7,282) CYCLOPHOSPHAMIDE (7,100) DOXORUBICIN (6,165) VINCRISTINE (5,252) PREDNISONE (5,096) BEVACIZUMAB (4,653) DEXAMETHASONE (4,545) CARBOPLATIN (4,538) CAPECITABINE (3,808) ETOPOSIDE (3,776)

Related Pages

ETRUMADENANT Full Profile All Disease progression Reports All Drugs Causing Disease progression ETRUMADENANT Demographics