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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 CRIZOTINIB Cause Blood count abnormal? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Blood count abnormal have been filed in association with CRIZOTINIB (Xalkori). This represents 0.1% of all adverse event reports for CRIZOTINIB.

8
Reports of Blood count abnormal with CRIZOTINIB
0.1%
of all CRIZOTINIB reports
1
Deaths
4
Hospitalizations

How Dangerous Is Blood count abnormal From CRIZOTINIB?

Of the 8 reports, 1 (12.5%) resulted in death, 4 (50.0%) required hospitalization.

Is Blood count abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CRIZOTINIB. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does CRIZOTINIB Cause?

Death (2,028) Neoplasm progression (1,161) Nausea (820) Disease progression (677) Diarrhoea (631) Vomiting (600) Fatigue (419) Off label use (353) Dyspnoea (352) Visual impairment (315)

What Other Drugs Cause Blood count abnormal?

ALBUTEROL (3,248) TIOTROPIUM (1,677) PREDNISONE (1,600) BUDESONIDE\FORMOTEROL (1,595) MONTELUKAST (1,264) PALBOCICLIB (1,169) MEPOLIZUMAB (1,157) RUXOLITINIB (1,080) FLUTICASONE\SALMETEROL (841) LENALIDOMIDE (701)

Which CRIZOTINIB Alternatives Have Lower Blood count abnormal Risk?

CRIZOTINIB vs CROFELEMER CRIZOTINIB vs CROMOLYN CRIZOTINIB vs CROTALIDAE POLYVALENT IMMUNE FAB CRIZOTINIB vs CUBICIN CRIZOTINIB vs CUPRIC

Related Pages

CRIZOTINIB Full Profile All Blood count abnormal Reports All Drugs Causing Blood count abnormal CRIZOTINIB Demographics