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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 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

Related Pages

KETOPROFEN Full Profile All Multi-organ failure Reports All Drugs Causing Multi-organ failure KETOPROFEN Demographics