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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 ACETAMINOPHEN\NAPROXEN Cause Rheumatoid arthritis? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Rheumatoid arthritis have been filed in association with ACETAMINOPHEN\NAPROXEN. This represents 73.9% of all adverse event reports for ACETAMINOPHEN\NAPROXEN.

17
Reports of Rheumatoid arthritis with ACETAMINOPHEN\NAPROXEN
73.9%
of all ACETAMINOPHEN\NAPROXEN reports
9
Deaths
9
Hospitalizations

How Dangerous Is Rheumatoid arthritis From ACETAMINOPHEN\NAPROXEN?

Of the 17 reports, 9 (52.9%) resulted in death, 9 (52.9%) required hospitalization, and 9 (52.9%) were considered life-threatening.

Is Rheumatoid arthritis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ACETAMINOPHEN\NAPROXEN. However, 17 reports have been filed with the FAERS database.

What Other Side Effects Does ACETAMINOPHEN\NAPROXEN Cause?

Off label use (19) Drug ineffective (18) Contraindicated product administered (17) Pain (17) Swelling (17) Synovitis (17) Condition aggravated (16) Rash (16) Arthralgia (15) Drug intolerance (14)

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)

Related Pages

ACETAMINOPHEN\NAPROXEN Full Profile All Rheumatoid arthritis Reports All Drugs Causing Rheumatoid arthritis ACETAMINOPHEN\NAPROXEN Demographics