Does KETOPROFEN Cause Multi-organ failure? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Multi-organ failure have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.
6
Reports of Multi-organ failure with KETOPROFEN
0.1%
of all KETOPROFEN reports
6
Deaths
4
Hospitalizations
How Dangerous Is Multi-organ failure From KETOPROFEN?
Of the 6 reports, 6 (100.0%) resulted in death, 4 (66.7%) required hospitalization.
Is Multi-organ failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 6 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 Multi-organ failure?
CYCLOPHOSPHAMIDE (151)
METHOTREXATE (130)
CYTARABINE (117)
METFORMIN (115)
PREDNISONE (106)
DOXORUBICIN (104)
DEXAMETHASONE (103)
CYCLOSPORINE (99)
VINCRISTINE (98)
PREDNISOLONE (96)
Which KETOPROFEN Alternatives Have Lower Multi-organ failure Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN