Does KETOPROFEN Cause Rheumatoid arthritis? 493 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 493 reports of Rheumatoid arthritis have been filed in association with KETOPROFEN (Orudis). This represents 8.9% of all adverse event reports for KETOPROFEN.
493
Reports of Rheumatoid arthritis with KETOPROFEN
8.9%
of all KETOPROFEN reports
109
Deaths
16
Hospitalizations
How Dangerous Is Rheumatoid arthritis From KETOPROFEN?
Of the 493 reports, 109 (22.1%) resulted in death, 16 (3.2%) required hospitalization, and 6 (1.2%) were considered life-threatening.
Is Rheumatoid arthritis Listed in the Official Label?
Yes, Rheumatoid arthritis is listed as a known adverse reaction in the official FDA drug label for KETOPROFEN.
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)
Immunodeficiency (492)
Rash erythematous (485)
What Other Drugs Cause Rheumatoid arthritis?
ETANERCEPT (33,166)
ADALIMUMAB (29,817)
METHOTREXATE (29,254)
ABATACEPT (21,898)
LEFLUNOMIDE (20,886)
TOCILIZUMAB (20,652)
HYDROXYCHLOROQUINE (20,110)
RITUXIMAB (19,850)
CERTOLIZUMAB PEGOL (17,782)
INFLIXIMAB (16,251)
Which KETOPROFEN Alternatives Have Lower Rheumatoid arthritis Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN