Does ACETAMINOPHEN\NAPROXEN Cause Condition aggravated? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Condition aggravated have been filed in association with ACETAMINOPHEN\NAPROXEN. This represents 69.6% of all adverse event reports for ACETAMINOPHEN\NAPROXEN.
16
Reports of Condition aggravated with ACETAMINOPHEN\NAPROXEN
69.6%
of all ACETAMINOPHEN\NAPROXEN reports
8
Deaths
8
Hospitalizations
How Dangerous Is Condition aggravated From ACETAMINOPHEN\NAPROXEN?
Of the 16 reports, 8 (50.0%) resulted in death, 8 (50.0%) required hospitalization, and 8 (50.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACETAMINOPHEN\NAPROXEN. However, 16 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)
Rheumatoid arthritis (17)
Swelling (17)
Synovitis (17)
Rash (16)
Arthralgia (15)
Drug intolerance (14)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)