Does DUVELISIB Cause Haemoglobin decreased? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Haemoglobin decreased have been filed in association with DUVELISIB (COPIKTRA). This represents 0.9% of all adverse event reports for DUVELISIB.
7
Reports of Haemoglobin decreased with DUVELISIB
0.9%
of all DUVELISIB reports
1
Deaths
1
Hospitalizations
How Dangerous Is Haemoglobin decreased From DUVELISIB?
Of the 7 reports, 1 (14.3%) resulted in death, 1 (14.3%) required hospitalization.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUVELISIB. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does DUVELISIB Cause?
Product use in unapproved indication (162)
Diarrhoea (110)
Death (89)
Fatigue (75)
Prescribed underdose (63)
Off label use (57)
Nausea (49)
Pneumonia (40)
Pyrexia (40)
Malignant neoplasm progression (38)
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 DUVELISIB Alternatives Have Lower Haemoglobin decreased Risk?
DUVELISIB vs DYDROGESTERONE
DUVELISIB vs EBASTINE
DUVELISIB vs ECALLANTIDE
DUVELISIB vs ECONAZOLE
DUVELISIB vs ECULIZUMAB