Does DAROLUTAMIDE Cause Full blood count abnormal? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Full blood count abnormal have been filed in association with DAROLUTAMIDE (NUBEQA). This represents 0.2% of all adverse event reports for DAROLUTAMIDE.
7
Reports of Full blood count abnormal with DAROLUTAMIDE
0.2%
of all DAROLUTAMIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Full blood count abnormal From DAROLUTAMIDE?
Of the 7 reports, 2 (28.6%) required hospitalization.
Is Full blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DAROLUTAMIDE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does DAROLUTAMIDE Cause?
Fatigue (384)
Death (361)
Hot flush (203)
Asthenia (173)
Prostatic specific antigen increased (156)
Off label use (133)
Neuropathy peripheral (127)
Diarrhoea (122)
Dizziness (122)
Rash (116)
What Other Drugs Cause Full blood count abnormal?
ALBUTEROL (3,060)
PREDNISONE (2,230)
BUDESONIDE\FORMOTEROL (1,786)
TIOTROPIUM (1,754)
MONTELUKAST (1,529)
MEPOLIZUMAB (1,440)
BUDESONIDE (1,339)
PALBOCICLIB (1,146)
CICLESONIDE (916)
PANTOPRAZOLE (776)
Which DAROLUTAMIDE Alternatives Have Lower Full blood count abnormal Risk?
DAROLUTAMIDE vs DARUNAVIR
DAROLUTAMIDE vs DARUNAVIR ETHANOLATE
DAROLUTAMIDE vs DARUNAVIR\RITONAVIR
DAROLUTAMIDE vs DASABUVIR
DAROLUTAMIDE vs DASABUVIR\OMBITASVIR HEMINONAHYDRATE\PARITAPREVIR\RITONAVIR