Does DUVELISIB Cause Dehydration? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Dehydration have been filed in association with DUVELISIB (COPIKTRA). This represents 2.8% of all adverse event reports for DUVELISIB.
21
Reports of Dehydration with DUVELISIB
2.8%
of all DUVELISIB reports
4
Deaths
16
Hospitalizations
How Dangerous Is Dehydration From DUVELISIB?
Of the 21 reports, 4 (19.0%) resulted in death, 16 (76.2%) required hospitalization.
Is Dehydration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUVELISIB. However, 21 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)