Does ACETAMINOPHEN\NAPROXEN Cause Duodenal ulcer perforation? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Duodenal ulcer perforation have been filed in association with ACETAMINOPHEN\NAPROXEN. This represents 39.1% of all adverse event reports for ACETAMINOPHEN\NAPROXEN.
9
Reports of Duodenal ulcer perforation with ACETAMINOPHEN\NAPROXEN
39.1%
of all ACETAMINOPHEN\NAPROXEN reports
9
Deaths
9
Hospitalizations
How Dangerous Is Duodenal ulcer perforation 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 Duodenal ulcer perforation 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 Duodenal ulcer perforation?
METHOTREXATE (4,239)
LEFLUNOMIDE (4,200)
FOLIC ACID (4,152)
ABATACEPT (4,147)
TOCILIZUMAB (4,130)
DICLOFENAC (4,120)
CETIRIZINE (4,117)
DESOXIMETASONE (4,084)
RITUXIMAB (4,081)
PREDNISONE (4,060)