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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 Unevaluable event? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Unevaluable event have been filed in association with CRIZOTINIB (Xalkori). This represents 0.1% of all adverse event reports for CRIZOTINIB.

6
Reports of Unevaluable event with CRIZOTINIB
0.1%
of all CRIZOTINIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Unevaluable event From CRIZOTINIB?

Of the 6 reports, 1 (16.7%) required hospitalization.

Is Unevaluable event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CRIZOTINIB. However, 6 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 Unevaluable event?

ADALIMUMAB (4,242) ETANERCEPT (3,902) LENALIDOMIDE (3,331) OXYCODONE (3,145) AMBRISENTAN (2,336) SODIUM OXYBATE (2,328) CARBIDOPA\LEVODOPA (1,632) DUPILUMAB (1,410) MORPHINE (1,161) ACETAMINOPHEN\HYDROCODONE (1,118)

Which CRIZOTINIB Alternatives Have Lower Unevaluable event 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 Unevaluable event Reports All Drugs Causing Unevaluable event CRIZOTINIB Demographics