Does RUCAPARIB CAMSYLATE Cause Adverse event? 571 Reports in FDA Database
Prostate Health & Male Vitality — Naturally
ProstaVive: better flow, better sleep, better energy. 180-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 571 reports of Adverse event have been filed in association with RUCAPARIB CAMSYLATE (Rubraca). This represents 6.9% of all adverse event reports for RUCAPARIB CAMSYLATE.
571
Reports of Adverse event with RUCAPARIB CAMSYLATE
6.9%
of all RUCAPARIB CAMSYLATE reports
22
Deaths
269
Hospitalizations
How Dangerous Is Adverse event From RUCAPARIB CAMSYLATE?
Of the 571 reports, 22 (3.9%) resulted in death, 269 (47.1%) required hospitalization, and 2 (0.4%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for RUCAPARIB CAMSYLATE.
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)
Carbohydrate antigen 125 increased (562)
Dysgeusia (558)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which RUCAPARIB CAMSYLATE Alternatives Have Lower Adverse event Risk?
RUCAPARIB CAMSYLATE vs RUFINAMIDE
RUCAPARIB CAMSYLATE vs RUPATADINE
RUCAPARIB CAMSYLATE vs RUXOLITINIB
RUCAPARIB CAMSYLATE vs SABRIL
RUCAPARIB CAMSYLATE vs SACCHAROMYCES CEREVISIAE