Does FLURBIPROFEN AXETIL Cause Hepatic function abnormal? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Hepatic function abnormal have been filed in association with FLURBIPROFEN AXETIL. This represents 23.5% of all adverse event reports for FLURBIPROFEN AXETIL.
20
Reports of Hepatic function abnormal with FLURBIPROFEN AXETIL
23.5%
of all FLURBIPROFEN AXETIL reports
1
Deaths
11
Hospitalizations
How Dangerous Is Hepatic function abnormal From FLURBIPROFEN AXETIL?
Of the 20 reports, 1 (5.0%) resulted in death, 11 (55.0%) required hospitalization, and 6 (30.0%) 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 FLURBIPROFEN AXETIL. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does FLURBIPROFEN AXETIL Cause?
Diarrhoea (8)
Acute kidney injury (5)
Adenovirus infection (5)
Anaphylactic shock (5)
Graft versus host disease (5)
Hyperglycaemia (5)
Ileus paralytic (5)
Pneumothorax (5)
Pyrexia (5)
Respiratory disorder (5)
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)