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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 Dyspnoea? 121 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 121 reports of Dyspnoea have been filed in association with BRIGATINIB (Alunbrig). This represents 3.7% of all adverse event reports for BRIGATINIB.

121
Reports of Dyspnoea with BRIGATINIB
3.7%
of all BRIGATINIB reports
21
Deaths
52
Hospitalizations

How Dangerous Is Dyspnoea From BRIGATINIB?

Of the 121 reports, 21 (17.4%) resulted in death, 52 (43.0%) required hospitalization, and 2 (1.7%) 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 BRIGATINIB. However, 121 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 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 BRIGATINIB Alternatives Have Lower Dyspnoea Risk?

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

Related Pages

BRIGATINIB Full Profile All Dyspnoea Reports All Drugs Causing Dyspnoea BRIGATINIB Demographics