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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 BRIGATINIB Cause Adverse event? 22 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Adverse event have been filed in association with BRIGATINIB (Alunbrig). This represents 0.7% of all adverse event reports for BRIGATINIB.

22
Reports of Adverse event with BRIGATINIB
0.7%
of all BRIGATINIB reports
10
Deaths
9
Hospitalizations

How Dangerous Is Adverse event From BRIGATINIB?

Of the 22 reports, 10 (45.5%) resulted in death, 9 (40.9%) required hospitalization.

Is Adverse event Listed in the Official Label?

Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for BRIGATINIB.

What Other Side Effects Does BRIGATINIB Cause?

Death (405) Non-small cell lung cancer (370) Off label use (256) Diarrhoea (239) Metastases to central nervous system (219) Nausea (218) Lung neoplasm malignant (216) Fatigue (201) Blood creatine phosphokinase increased (198) Product dose omission issue (193)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which BRIGATINIB Alternatives Have Lower Adverse event Risk?

BRIGATINIB vs BRILINTA BRIGATINIB vs BRILIQUE BRIGATINIB vs BRIMONIDINE BRIGATINIB vs BRIMONIDINE\BRINZOLAMIDE BRIGATINIB vs BRIMONIDINE\TIMOLOL

Related Pages

BRIGATINIB Full Profile All Adverse event Reports All Drugs Causing Adverse event BRIGATINIB Demographics