Does ACETAMINOPHEN\NAPROXEN Cause Product use issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product use issue have been filed in association with ACETAMINOPHEN\NAPROXEN. This represents 39.1% of all adverse event reports for ACETAMINOPHEN\NAPROXEN.
9
Reports of Product use issue with ACETAMINOPHEN\NAPROXEN
39.1%
of all ACETAMINOPHEN\NAPROXEN reports
9
Deaths
9
Hospitalizations
How Dangerous Is Product use issue From ACETAMINOPHEN\NAPROXEN?
Of the 9 reports, 9 (100.0%) resulted in death, 9 (100.0%) required hospitalization, and 9 (100.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACETAMINOPHEN\NAPROXEN. However, 9 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)
Condition aggravated (16)
Rash (16)
Arthralgia (15)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)