Does BRIGATINIB Cause Product administration error? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product administration error have been filed in association with BRIGATINIB (Alunbrig). This represents 0.2% of all adverse event reports for BRIGATINIB.
8
Reports of Product administration error with BRIGATINIB
0.2%
of all BRIGATINIB reports
4
Deaths
4
Hospitalizations
How Dangerous Is Product administration error From BRIGATINIB?
Of the 8 reports, 4 (50.0%) resulted in death, 4 (50.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIGATINIB. However, 8 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which BRIGATINIB Alternatives Have Lower Product administration error Risk?
BRIGATINIB vs BRILINTA
BRIGATINIB vs BRILIQUE
BRIGATINIB vs BRIMONIDINE
BRIGATINIB vs BRIMONIDINE\BRINZOLAMIDE
BRIGATINIB vs BRIMONIDINE\TIMOLOL