Does BRIGATINIB Cause Product dose omission issue? 193 Reports in FDA Database
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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
18
Deaths
70
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 (216)
Fatigue (201)
Blood creatine phosphokinase increased (198)
Neoplasm progression (172)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which BRIGATINIB Alternatives Have Lower Product dose omission issue Risk?
BRIGATINIB vs BRILINTA
BRIGATINIB vs BRILIQUE
BRIGATINIB vs BRIMONIDINE
BRIGATINIB vs BRIMONIDINE\BRINZOLAMIDE
BRIGATINIB vs BRIMONIDINE\TIMOLOL