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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 Skin lesion? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Skin lesion have been filed in association with KETOPROFEN (Orudis). This represents 0.2% of all adverse event reports for KETOPROFEN.

12
Reports of Skin lesion with KETOPROFEN
0.2%
of all KETOPROFEN reports
0
Deaths
9
Hospitalizations

How Dangerous Is Skin lesion From KETOPROFEN?

Of the 12 reports, 9 (75.0%) required hospitalization.

Is Skin lesion Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 12 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 Skin lesion?

SECUKINUMAB (1,909) ADALIMUMAB (1,507) METHOTREXATE (1,237) DUPILUMAB (685) ETANERCEPT (647) PREDNISONE (617) TOFACITINIB (478) INFLIXIMAB (474) CYCLOSPORINE (380) LENALIDOMIDE (369)

Which KETOPROFEN Alternatives Have Lower Skin lesion 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 Skin lesion Reports All Drugs Causing Skin lesion KETOPROFEN Demographics