Does KETOPROFEN Cause Hepatitis cholestatic? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Hepatitis cholestatic have been filed in association with KETOPROFEN (Orudis). This represents 0.6% of all adverse event reports for KETOPROFEN.
32
Reports of Hepatitis cholestatic with KETOPROFEN
0.6%
of all KETOPROFEN reports
0
Deaths
26
Hospitalizations
How Dangerous Is Hepatitis cholestatic From KETOPROFEN?
Of the 32 reports, 26 (81.3%) required hospitalization, and 4 (12.5%) were considered life-threatening.
Is Hepatitis cholestatic Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 32 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 cholestatic?
ATORVASTATIN (396)
ACETAMINOPHEN (356)
AMOXICILLIN\CLAVULANATE (190)
PANTOPRAZOLE (184)
AMOXICILLIN\CLAVULANIC ACID (178)
SULFAMETHOXAZOLE\TRIMETHOPRIM (143)
TACROLIMUS (119)
IBUPROFEN (110)
LEVOFLOXACIN (110)
PEMBROLIZUMAB (110)
Which KETOPROFEN Alternatives Have Lower Hepatitis cholestatic Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN