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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 Intentional dose omission? 89 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 89 reports of Intentional dose omission have been filed in association with NIRAPARIB (ZEJULA). This represents 0.4% of all adverse event reports for NIRAPARIB.

89
Reports of Intentional dose omission with NIRAPARIB
0.4%
of all NIRAPARIB reports
0
Deaths
32
Hospitalizations

How Dangerous Is Intentional dose omission From NIRAPARIB?

Of the 89 reports, 32 (36.0%) required hospitalization, and 2 (2.2%) were considered life-threatening.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NIRAPARIB. However, 89 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 Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which NIRAPARIB Alternatives Have Lower Intentional dose omission 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 Intentional dose omission Reports All Drugs Causing Intentional dose omission NIRAPARIB Demographics