Does NAPROXEN Cause Intentional product use issue? 1,796 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,796 reports of Intentional product use issue have been filed in association with NAPROXEN (Naproxen Sodium). This represents 3.4% of all adverse event reports for NAPROXEN.
1,796
Reports of Intentional product use issue with NAPROXEN
3.4%
of all NAPROXEN reports
874
Deaths
1,195
Hospitalizations
How Dangerous Is Intentional product use issue From NAPROXEN?
Of the 1,796 reports, 874 (48.7%) resulted in death, 1,195 (66.5%) required hospitalization, and 1,120 (62.4%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 1,796 reports have been filed with the FAERS database.
What Other Side Effects Does NAPROXEN Cause?
Drug ineffective (12,416)
Product use issue (4,865)
Off label use (4,434)
Drug hypersensitivity (4,160)
Pain (4,140)
Nausea (4,139)
Vomiting (3,889)
Fatigue (3,659)
Diarrhoea (3,498)
Dizziness (3,460)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which NAPROXEN Alternatives Have Lower Intentional product use issue Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX