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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 Full blood count abnormal? 338 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 338 reports of Full blood count abnormal have been filed in association with NIRAPARIB (ZEJULA). This represents 1.6% of all adverse event reports for NIRAPARIB.

338
Reports of Full blood count abnormal with NIRAPARIB
1.6%
of all NIRAPARIB reports
5
Deaths
77
Hospitalizations

How Dangerous Is Full blood count abnormal From NIRAPARIB?

Of the 338 reports, 5 (1.5%) resulted in death, 77 (22.8%) required hospitalization, and 2 (0.6%) were considered life-threatening.

Is Full blood count abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NIRAPARIB. However, 338 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 Full blood count abnormal?

ALBUTEROL (3,060) PREDNISONE (2,230) BUDESONIDE\FORMOTEROL (1,786) TIOTROPIUM (1,754) MONTELUKAST (1,529) MEPOLIZUMAB (1,440) BUDESONIDE (1,339) PALBOCICLIB (1,146) CICLESONIDE (916) PANTOPRAZOLE (776)

Which NIRAPARIB Alternatives Have Lower Full blood count abnormal 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 Full blood count abnormal Reports All Drugs Causing Full blood count abnormal NIRAPARIB Demographics