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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 Hyponatraemia? 61 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Hyponatraemia have been filed in association with CRIZOTINIB (Xalkori). This represents 0.6% of all adverse event reports for CRIZOTINIB.

61
Reports of Hyponatraemia with CRIZOTINIB
0.6%
of all CRIZOTINIB reports
9
Deaths
45
Hospitalizations

How Dangerous Is Hyponatraemia From CRIZOTINIB?

Of the 61 reports, 9 (14.8%) resulted in death, 45 (73.8%) required hospitalization, and 12 (19.7%) were considered life-threatening.

Is Hyponatraemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CRIZOTINIB. However, 61 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 Hyponatraemia?

FUROSEMIDE (3,127) HYDROCHLOROTHIAZIDE (2,138) OMEPRAZOLE (1,635) LANSOPRAZOLE (1,416) SERTRALINE (1,332) RAMIPRIL (1,178) SPIRONOLACTONE (1,166) PANTOPRAZOLE (1,134) INDAPAMIDE (976) AMLODIPINE (879)

Which CRIZOTINIB Alternatives Have Lower Hyponatraemia 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 Hyponatraemia Reports All Drugs Causing Hyponatraemia CRIZOTINIB Demographics