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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 Bursitis? 389 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 389 reports of Bursitis have been filed in association with KETOPROFEN (Orudis). This represents 7.0% of all adverse event reports for KETOPROFEN.

389
Reports of Bursitis with KETOPROFEN
7.0%
of all KETOPROFEN reports
108
Deaths
3
Hospitalizations

How Dangerous Is Bursitis From KETOPROFEN?

Of the 389 reports, 108 (27.8%) resulted in death, 3 (0.8%) required hospitalization, and 5 (1.3%) were considered life-threatening.

Is Bursitis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 389 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 Bursitis?

ADALIMUMAB (2,448) TOCILIZUMAB (2,094) RITUXIMAB (2,075) METHOTREXATE (2,060) ABATACEPT (1,903) ALENDRONATE (1,873) ETANERCEPT (1,768) SECUKINUMAB (1,755) LEFLUNOMIDE (1,728) CETIRIZINE (1,706)

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