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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 Immunodeficiency? 492 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 492 reports of Immunodeficiency have been filed in association with KETOPROFEN (Orudis). This represents 8.9% of all adverse event reports for KETOPROFEN.

492
Reports of Immunodeficiency with KETOPROFEN
8.9%
of all KETOPROFEN reports
114
Deaths
8
Hospitalizations

How Dangerous Is Immunodeficiency From KETOPROFEN?

Of the 492 reports, 114 (23.2%) resulted in death, 8 (1.6%) required hospitalization, and 8 (1.6%) were considered life-threatening.

Is Immunodeficiency Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 492 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) Rash erythematous (485)

What Other Drugs Cause Immunodeficiency?

ADALIMUMAB (2,981) RITUXIMAB (1,256) TOCILIZUMAB (1,061) ABATACEPT (1,042) METHOTREXATE (926) ETANERCEPT (799) INFLIXIMAB (693) CETIRIZINE (650) METHYLPREDNISOLONE (615) ALBUTEROL (599)

Which KETOPROFEN Alternatives Have Lower Immunodeficiency 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 Immunodeficiency Reports All Drugs Causing Immunodeficiency KETOPROFEN Demographics