Does KETOPROFEN Cause Acute hepatic failure? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Acute hepatic failure have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.
16
Reports of Acute hepatic failure with KETOPROFEN
0.3%
of all KETOPROFEN reports
0
Deaths
14
Hospitalizations
How Dangerous Is Acute hepatic failure From KETOPROFEN?
Of the 16 reports, 14 (87.5%) required hospitalization, and 11 (68.8%) were considered life-threatening.
Is Acute hepatic failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 16 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 Acute hepatic failure?
ACETAMINOPHEN (3,141)
PREDNISONE (439)
IBUPROFEN (412)
RITUXIMAB (412)
CYCLOPHOSPHAMIDE (411)
DOXORUBICIN (385)
VINCRISTINE (346)
PREDNISOLONE (301)
METHOTREXATE (285)
DEXAMETHASONE (249)
Which KETOPROFEN Alternatives Have Lower Acute hepatic failure Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN