Does KETOPROFEN 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 KETOPROFEN (Orudis). This represents 0.4% of all adverse event reports for KETOPROFEN.
20
Reports of Hepatic function abnormal with KETOPROFEN
0.4%
of all KETOPROFEN reports
1
Deaths
10
Hospitalizations
How Dangerous Is Hepatic function abnormal From KETOPROFEN?
Of the 20 reports, 1 (5.0%) resulted in death, 10 (50.0%) required hospitalization, and 7 (35.0%) 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 KETOPROFEN. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does KETOPROFEN Cause?
Pain (595)
Headache (574)
Hypersensitivity (556)
Erythema (546)
Acute kidney injury (517)
Hyperhidrosis (516)
Hepatic enzyme increased (508)
Asthma (507)
Rheumatoid arthritis (493)
Immunodeficiency (492)
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 KETOPROFEN Alternatives Have Lower Hepatic function abnormal Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN