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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 Haemoglobin abnormal? 68 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Haemoglobin abnormal have been filed in association with NIRAPARIB (ZEJULA). This represents 0.3% of all adverse event reports for NIRAPARIB.

68
Reports of Haemoglobin abnormal with NIRAPARIB
0.3%
of all NIRAPARIB reports
1
Deaths
24
Hospitalizations

How Dangerous Is Haemoglobin abnormal From NIRAPARIB?

Of the 68 reports, 1 (1.5%) resulted in death, 24 (35.3%) required hospitalization, and 1 (1.5%) were considered life-threatening.

Is Haemoglobin abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NIRAPARIB. However, 68 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 Haemoglobin abnormal?

RUXOLITINIB (500) ECULIZUMAB (466) VENETOCLAX (248) DARBEPOETIN ALFA (213) ADALIMUMAB (207) LENALIDOMIDE (172) RITUXIMAB (157) ERYTHROPOIETIN (154) IBRUTINIB (148) DEXAMETHASONE (147)

Which NIRAPARIB Alternatives Have Lower Haemoglobin 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 Haemoglobin abnormal Reports All Drugs Causing Haemoglobin abnormal NIRAPARIB Demographics