Does BRIGATINIB Cause Product dose omission issue? 193 Reports in FDA Database

Q: Does BRIGATINIB cause Product dose omission issue?

193 reports of Product dose omission issue have been filed with the FDA for BRIGATINIB, representing 5.9% of all BRIGATINIB adverse event reports.

Q: How dangerous is Product dose omission issue from BRIGATINIB?

Of 193 reports, 18 (9.3%) resulted in death and 70 required hospitalization.

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According to the FDA Adverse Event Reporting System (FAERS), 193 reports of Product dose omission issue have been filed in association with BRIGATINIB (Alunbrig). This represents 5.9% of all adverse event reports for BRIGATINIB.

193

Reports of Product dose omission issue with BRIGATINIB

5.9%

of all BRIGATINIB reports

Deaths

Hospitalizations

How Dangerous Is Product dose omission issue From BRIGATINIB?

Of the 193 reports, 18 (9.3%) resulted in death, 70 (36.3%) required hospitalization, and 2 (1.0%) were considered life-threatening.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIGATINIB. However, 193 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 ( 503 Service Unavailable

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