Does BRIGATINIB Cause Hepatic function abnormal? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Hepatic function abnormal have been filed in association with BRIGATINIB (Alunbrig). This represents 1.0% of all adverse event reports for BRIGATINIB.
33
Reports of Hepatic function abnormal with BRIGATINIB
1.0%
of all BRIGATINIB reports
0
Deaths
20
Hospitalizations
How Dangerous Is Hepatic function abnormal From BRIGATINIB?
Of the 33 reports, 20 (60.6%) required hospitalization, and 1 (3.0%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIGATINIB. However, 33 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 Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which BRIGATINIB Alternatives Have Lower Hepatic function abnormal Risk?
BRIGATINIB vs BRILINTA
BRIGATINIB vs BRILIQUE
BRIGATINIB vs BRIMONIDINE
BRIGATINIB vs BRIMONIDINE\BRINZOLAMIDE
BRIGATINIB vs BRIMONIDINE\TIMOLOL