Does RUCAPARIB CAMSYLATE Cause Blood count abnormal? 196 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 196 reports of Blood count abnormal have been filed in association with RUCAPARIB CAMSYLATE (Rubraca). This represents 2.4% of all adverse event reports for RUCAPARIB CAMSYLATE.
196
Reports of Blood count abnormal with RUCAPARIB CAMSYLATE
2.4%
of all RUCAPARIB CAMSYLATE reports
3
Deaths
47
Hospitalizations
How Dangerous Is Blood count abnormal From RUCAPARIB CAMSYLATE?
Of the 196 reports, 3 (1.5%) resulted in death, 47 (24.0%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RUCAPARIB CAMSYLATE. However, 196 reports have been filed with the FAERS database.
What Other Side Effects Does RUCAPARIB CAMSYLATE Cause?
Fatigue (2,494)
Nausea (2,219)
Malignant neoplasm progression (1,162)
Decreased appetite (787)
Constipation (763)
Diarrhoea (759)
Vomiting (759)
Asthenia (660)
Adverse event (571)
Carbohydrate antigen 125 increased (562)
What Other Drugs Cause Blood count abnormal?
ALBUTEROL (3,248)
TIOTROPIUM (1,677)
PREDNISONE (1,600)
BUDESONIDE\FORMOTEROL (1,595)
MONTELUKAST (1,264)
PALBOCICLIB (1,169)
MEPOLIZUMAB (1,157)
RUXOLITINIB (1,080)
FLUTICASONE\SALMETEROL (841)
LENALIDOMIDE (701)
Which RUCAPARIB CAMSYLATE Alternatives Have Lower Blood count abnormal Risk?
RUCAPARIB CAMSYLATE vs RUFINAMIDE
RUCAPARIB CAMSYLATE vs RUPATADINE
RUCAPARIB CAMSYLATE vs RUXOLITINIB
RUCAPARIB CAMSYLATE vs SABRIL
RUCAPARIB CAMSYLATE vs SACCHAROMYCES CEREVISIAE