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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 Therapy non-responder? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Therapy non-responder have been filed in association with BRIGATINIB (Alunbrig). This represents 0.2% of all adverse event reports for BRIGATINIB.

6
Reports of Therapy non-responder with BRIGATINIB
0.2%
of all BRIGATINIB reports
1
Deaths
2
Hospitalizations

How Dangerous Is Therapy non-responder From BRIGATINIB?

Of the 6 reports, 1 (16.7%) resulted in death, 2 (33.3%) required hospitalization.

Is Therapy non-responder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIGATINIB. However, 6 reports have been filed with the FAERS database.

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 Therapy non-responder?

ETANERCEPT (3,472) APREMILAST (3,360) METHOTREXATE (2,965) RITUXIMAB (2,731) ADALIMUMAB (2,595) PREDNISONE (2,563) TREPROSTINIL (2,289) INFLIXIMAB (2,122) TOCILIZUMAB (1,775) HYDROXYCHLOROQUINE (1,699)

Which BRIGATINIB Alternatives Have Lower Therapy non-responder Risk?

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

Related Pages

BRIGATINIB Full Profile All Therapy non-responder Reports All Drugs Causing Therapy non-responder BRIGATINIB Demographics