Does ETRUMADENANT Cause Haemoglobin decreased? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Haemoglobin decreased have been filed in association with ETRUMADENANT. This represents 7.1% of all adverse event reports for ETRUMADENANT.
5
Reports of Haemoglobin decreased with ETRUMADENANT
7.1%
of all ETRUMADENANT reports
1
Deaths
4
Hospitalizations
How Dangerous Is Haemoglobin decreased From ETRUMADENANT?
Of the 5 reports, 1 (20.0%) resulted in death, 4 (80.0%) required hospitalization, and 3 (60.0%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETRUMADENANT. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does ETRUMADENANT Cause?
Disease progression (19)
Febrile neutropenia (16)
Platelet count decreased (15)
Pyrexia (14)
Hyponatraemia (12)
Drug hypersensitivity (11)
Vomiting (11)
Diarrhoea (10)
Nausea (10)
Acute kidney injury (7)
What Other Drugs Cause Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)