Does DUVELISIB Cause Prescribed underdose? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Prescribed underdose have been filed in association with DUVELISIB (COPIKTRA). This represents 8.3% of all adverse event reports for DUVELISIB.
63
Reports of Prescribed underdose with DUVELISIB
8.3%
of all DUVELISIB reports
8
Deaths
18
Hospitalizations
How Dangerous Is Prescribed underdose From DUVELISIB?
Of the 63 reports, 8 (12.7%) resulted in death, 18 (28.6%) required hospitalization.
Is Prescribed underdose Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUVELISIB. However, 63 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)
Off label use (57)
Nausea (49)
Pneumonia (40)
Pyrexia (40)
Malignant neoplasm progression (38)
Rash (33)
What Other Drugs Cause Prescribed underdose?
NATALIZUMAB (2,162)
SACUBITRIL\VALSARTAN (1,864)
APIXABAN (1,469)
ABATACEPT (1,192)
PIMAVANSERIN (1,165)
FINGOLIMOD (1,114)
RITUXIMAB (1,067)
METHOTREXATE (1,066)
ADALIMUMAB (1,010)
TOCILIZUMAB (1,002)
Which DUVELISIB Alternatives Have Lower Prescribed underdose Risk?
DUVELISIB vs DYDROGESTERONE
DUVELISIB vs EBASTINE
DUVELISIB vs ECALLANTIDE
DUVELISIB vs ECONAZOLE
DUVELISIB vs ECULIZUMAB