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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 Dyspnoea? 352 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 352 reports of Dyspnoea have been filed in association with CRIZOTINIB (Xalkori). This represents 3.5% of all adverse event reports for CRIZOTINIB.

352
Reports of Dyspnoea with CRIZOTINIB
3.5%
of all CRIZOTINIB reports
110
Deaths
180
Hospitalizations

How Dangerous Is Dyspnoea From CRIZOTINIB?

Of the 352 reports, 110 (31.3%) resulted in death, 180 (51.1%) required hospitalization, and 11 (3.1%) were considered life-threatening.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CRIZOTINIB. However, 352 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) Visual impairment (315) Constipation (313)

What Other Drugs Cause Dyspnoea?

ALBUTEROL (21,856) TREPROSTINIL (16,348) AMBRISENTAN (13,367) PREDNISONE (12,830) BUDESONIDE\FORMOTEROL (11,158) TIOTROPIUM (10,863) ADALIMUMAB (10,547) DUPILUMAB (10,310) FLUTICASONE\SALMETEROL (9,783) MEPOLIZUMAB (9,192)

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