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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 NIRAPARIB Cause Product use issue? 264 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 264 reports of Product use issue have been filed in association with NIRAPARIB (ZEJULA). This represents 1.2% of all adverse event reports for NIRAPARIB.

264
Reports of Product use issue with NIRAPARIB
1.2%
of all NIRAPARIB reports
12
Deaths
41
Hospitalizations

How Dangerous Is Product use issue From NIRAPARIB?

Of the 264 reports, 12 (4.5%) resulted in death, 41 (15.5%) required hospitalization, and 4 (1.5%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NIRAPARIB. However, 264 reports have been filed with the FAERS database.

What Other Side Effects Does NIRAPARIB Cause?

Nausea (5,794) Fatigue (5,240) Constipation (4,128) Platelet count decreased (4,102) Insomnia (2,861) Blood pressure increased (2,464) Headache (2,383) Off label use (2,213) Vomiting (2,029) Carbohydrate antigen 125 increased (1,868)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which NIRAPARIB Alternatives Have Lower Product use issue Risk?

NIRAPARIB vs NIRMATRELVIR\RITONAVIR NIRAPARIB vs NIROGACESTAT NIRAPARIB vs NIROGACESTAT HYDROBROMIDE NIRAPARIB vs NIRSEVIMAB NIRAPARIB vs NIRSEVIMAB-ALIP

Related Pages

NIRAPARIB Full Profile All Product use issue Reports All Drugs Causing Product use issue NIRAPARIB Demographics