Does IBRUTINIB Cause Haemoglobin abnormal? 148 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 148 reports of Haemoglobin abnormal have been filed in association with IBRUTINIB (Imbruvica). This represents 0.2% of all adverse event reports for IBRUTINIB.
148
Reports of Haemoglobin abnormal with IBRUTINIB
0.2%
of all IBRUTINIB reports
12
Deaths
69
Hospitalizations
How Dangerous Is Haemoglobin abnormal From IBRUTINIB?
Of the 148 reports, 12 (8.1%) resulted in death, 69 (46.6%) required hospitalization, and 1 (0.7%) were considered life-threatening.
Is Haemoglobin abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBRUTINIB. However, 148 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 abnormal?
RUXOLITINIB (500)
ECULIZUMAB (466)
VENETOCLAX (248)
DARBEPOETIN ALFA (213)
ADALIMUMAB (207)
LENALIDOMIDE (172)
RITUXIMAB (157)
ERYTHROPOIETIN (154)
DEXAMETHASONE (147)
CYCLOPHOSPHAMIDE (122)
Which IBRUTINIB Alternatives Have Lower Haemoglobin abnormal Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE