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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does KETOPROFEN Cause Hepatitis acute? 34 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Hepatitis acute have been filed in association with KETOPROFEN (Orudis). This represents 0.6% of all adverse event reports for KETOPROFEN.

34
Reports of Hepatitis acute with KETOPROFEN
0.6%
of all KETOPROFEN reports
0
Deaths
26
Hospitalizations

How Dangerous Is Hepatitis acute From KETOPROFEN?

Of the 34 reports, 26 (76.5%) required hospitalization, and 4 (11.8%) were considered life-threatening.

Is Hepatitis acute Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 34 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 Hepatitis acute?

ACETAMINOPHEN (626) ATORVASTATIN (254) IBUPROFEN (157) METHOTREXATE (103) SULFAMETHOXAZOLE\TRIMETHOPRIM (93) ENOXAPARIN (90) METFORMIN (90) NIVOLUMAB (90) AMOXICILLIN\CLAVULANATE (89) AMIODARONE (80)

Which KETOPROFEN Alternatives Have Lower Hepatitis acute Risk?

KETOPROFEN vs KETOPROFEN LYSINE KETOPROFEN vs KETOROLAC TROMETHAMINE KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE KETOPROFEN vs KETOTIFEN KETOPROFEN vs KLONOPIN

Related Pages

KETOPROFEN Full Profile All Hepatitis acute Reports All Drugs Causing Hepatitis acute KETOPROFEN Demographics