Does RUCAPARIB CAMSYLATE Cause Anaemia? 496 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 496 reports of Anaemia have been filed in association with RUCAPARIB CAMSYLATE (Rubraca). This represents 6.0% of all adverse event reports for RUCAPARIB CAMSYLATE.
496
Reports of Anaemia with RUCAPARIB CAMSYLATE
6.0%
of all RUCAPARIB CAMSYLATE reports
14
Deaths
114
Hospitalizations
How Dangerous Is Anaemia From RUCAPARIB CAMSYLATE?
Of the 496 reports, 14 (2.8%) resulted in death, 114 (23.0%) required hospitalization, and 3 (0.6%) were considered life-threatening.
Is Anaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RUCAPARIB CAMSYLATE. However, 496 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 Anaemia?
LENALIDOMIDE (5,322)
CARBOPLATIN (5,312)
RIBAVIRIN (5,130)
ASPIRIN (4,568)
CYCLOPHOSPHAMIDE (4,486)
RITUXIMAB (4,399)
DEXAMETHASONE (4,352)
ADALIMUMAB (3,994)
PACLITAXEL (3,949)
METHOTREXATE (3,913)
Which RUCAPARIB CAMSYLATE Alternatives Have Lower Anaemia Risk?
RUCAPARIB CAMSYLATE vs RUFINAMIDE
RUCAPARIB CAMSYLATE vs RUPATADINE
RUCAPARIB CAMSYLATE vs RUXOLITINIB
RUCAPARIB CAMSYLATE vs SABRIL
RUCAPARIB CAMSYLATE vs SACCHAROMYCES CEREVISIAE