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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 Oedema peripheral? 303 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 303 reports of Oedema peripheral have been filed in association with CRIZOTINIB (Xalkori). This represents 3.1% of all adverse event reports for CRIZOTINIB.

303
Reports of Oedema peripheral with CRIZOTINIB
3.1%
of all CRIZOTINIB reports
36
Deaths
93
Hospitalizations

How Dangerous Is Oedema peripheral From CRIZOTINIB?

Of the 303 reports, 36 (11.9%) resulted in death, 93 (30.7%) required hospitalization, and 6 (2.0%) were considered life-threatening.

Is Oedema peripheral Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CRIZOTINIB. However, 303 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 Oedema peripheral?

AMBRISENTAN (2,959) TREPROSTINIL (2,816) ADALIMUMAB (2,356) LENALIDOMIDE (2,298) AMLODIPINE (2,076) PREDNISONE (2,029) METHOTREXATE (1,939) MACITENTAN (1,932) RITUXIMAB (1,698) TOCILIZUMAB (1,574)

Which CRIZOTINIB Alternatives Have Lower Oedema peripheral 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 Oedema peripheral Reports All Drugs Causing Oedema peripheral CRIZOTINIB Demographics