Does KETOPROFEN Cause Jaundice? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Jaundice have been filed in association with KETOPROFEN (Orudis). This represents 0.5% of all adverse event reports for KETOPROFEN.
29
Reports of Jaundice with KETOPROFEN
0.5%
of all KETOPROFEN reports
1
Deaths
20
Hospitalizations
How Dangerous Is Jaundice From KETOPROFEN?
Of the 29 reports, 1 (3.4%) resulted in death, 20 (69.0%) required hospitalization, and 6 (20.7%) were considered life-threatening.
Is Jaundice Listed in the Official Label?
Yes, Jaundice is listed as a known adverse reaction in the official FDA drug label for KETOPROFEN.
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 Jaundice?
RIBAVIRIN (647)
ACETAMINOPHEN (553)
ATORVASTATIN (518)
RIFAMPIN (336)
IBUPROFEN (334)
ECULIZUMAB (333)
METHOTREXATE (295)
OMBITASVIR\PARITAPREVIR\RITONAVIR (279)
AMOXICILLIN\CLAVULANATE (272)
DASABUVIR (247)
Which KETOPROFEN Alternatives Have Lower Jaundice Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN