Does RUCAPARIB CAMSYLATE Cause Intentional product use issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Intentional product use issue have been filed in association with RUCAPARIB CAMSYLATE (Rubraca). This represents 0.1% of all adverse event reports for RUCAPARIB CAMSYLATE.
8
Reports of Intentional product use issue with RUCAPARIB CAMSYLATE
0.1%
of all RUCAPARIB CAMSYLATE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From RUCAPARIB CAMSYLATE?
Of the 8 reports, 1 (12.5%) required hospitalization, and 1 (12.5%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RUCAPARIB CAMSYLATE. However, 8 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which RUCAPARIB CAMSYLATE Alternatives Have Lower Intentional product use issue Risk?
RUCAPARIB CAMSYLATE vs RUFINAMIDE
RUCAPARIB CAMSYLATE vs RUPATADINE
RUCAPARIB CAMSYLATE vs RUXOLITINIB
RUCAPARIB CAMSYLATE vs SABRIL
RUCAPARIB CAMSYLATE vs SACCHAROMYCES CEREVISIAE