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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does RUCAPARIB CAMSYLATE Cause Hypersensitivity? 50 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Hypersensitivity have been filed in association with RUCAPARIB CAMSYLATE (Rubraca). This represents 0.6% of all adverse event reports for RUCAPARIB CAMSYLATE.

50
Reports of Hypersensitivity with RUCAPARIB CAMSYLATE
0.6%
of all RUCAPARIB CAMSYLATE reports
0
Deaths
9
Hospitalizations

How Dangerous Is Hypersensitivity From RUCAPARIB CAMSYLATE?

Of the 50 reports, 9 (18.0%) required hospitalization.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity 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) Adverse event (571) Carbohydrate antigen 125 increased (562)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which RUCAPARIB CAMSYLATE Alternatives Have Lower Hypersensitivity Risk?

RUCAPARIB CAMSYLATE vs RUFINAMIDE RUCAPARIB CAMSYLATE vs RUPATADINE RUCAPARIB CAMSYLATE vs RUXOLITINIB RUCAPARIB CAMSYLATE vs SABRIL RUCAPARIB CAMSYLATE vs SACCHAROMYCES CEREVISIAE

Related Pages

RUCAPARIB CAMSYLATE Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity RUCAPARIB CAMSYLATE Demographics