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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 Extra dose administered? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Extra dose administered have been filed in association with RUCAPARIB CAMSYLATE (Rubraca). This represents 0.2% of all adverse event reports for RUCAPARIB CAMSYLATE.

12
Reports of Extra dose administered with RUCAPARIB CAMSYLATE
0.2%
of all RUCAPARIB CAMSYLATE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Extra dose administered From RUCAPARIB CAMSYLATE?

Of the 12 reports, 2 (16.7%) required hospitalization.

Is Extra dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RUCAPARIB CAMSYLATE. However, 12 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 Extra dose administered?

TIRZEPATIDE (6,774) DULAGLUTIDE (3,047) LORATADINE (1,556) DUPILUMAB (1,422) FEXOFENADINE (1,413) NAPROXEN (908) POLYETHYLENE GLYCOL 3350 (589) ACETAMINOPHEN (552) DALFAMPRIDINE (519) FLUTICASONE\SALMETEROL (499)

Which RUCAPARIB CAMSYLATE Alternatives Have Lower Extra dose administered 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 Extra dose administered Reports All Drugs Causing Extra dose administered RUCAPARIB CAMSYLATE Demographics