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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 Off label use? 256 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 256 reports of Off label use have been filed in association with BRIGATINIB (Alunbrig). This represents 7.8% of all adverse event reports for BRIGATINIB.

256
Reports of Off label use with BRIGATINIB
7.8%
of all BRIGATINIB reports
64
Deaths
73
Hospitalizations

How Dangerous Is Off label use From BRIGATINIB?

Of the 256 reports, 64 (25.0%) resulted in death, 73 (28.5%) required hospitalization, and 4 (1.6%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIGATINIB. However, 256 reports have been filed with the FAERS database.

What Other Side Effects Does BRIGATINIB Cause?

Death (405) Non-small cell lung cancer (370) 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) Neoplasm progression (172)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Which BRIGATINIB Alternatives Have Lower Off label use Risk?

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

Related Pages

BRIGATINIB Full Profile All Off label use Reports All Drugs Causing Off label use BRIGATINIB Demographics