Does IBRUTINIB Cause Haemoglobin decreased? 1,146 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,146 reports of Haemoglobin decreased have been filed in association with IBRUTINIB (Imbruvica). This represents 1.5% of all adverse event reports for IBRUTINIB.
1,146
Reports of Haemoglobin decreased with IBRUTINIB
1.5%
of all IBRUTINIB reports
88
Deaths
588
Hospitalizations
How Dangerous Is Haemoglobin decreased From IBRUTINIB?
Of the 1,146 reports, 88 (7.7%) resulted in death, 588 (51.3%) required hospitalization, and 15 (1.3%) 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 IBRUTINIB. However, 1,146 reports have been filed with the FAERS database.
What Other Side Effects Does IBRUTINIB Cause?
Death (8,007)
Off label use (5,446)
Fatigue (4,479)
Diarrhoea (3,903)
Atrial fibrillation (3,671)
Pneumonia (3,015)
Incorrect dose administered (2,752)
Contusion (2,712)
Fall (2,375)
Asthenia (2,200)
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)
Which IBRUTINIB Alternatives Have Lower Haemoglobin decreased Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE