Does NAPROXEN Cause Intentional product misuse? 944 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 944 reports of Intentional product misuse have been filed in association with NAPROXEN (Naproxen Sodium). This represents 1.8% of all adverse event reports for NAPROXEN.
944
Reports of Intentional product misuse with NAPROXEN
1.8%
of all NAPROXEN reports
114
Deaths
241
Hospitalizations
How Dangerous Is Intentional product misuse From NAPROXEN?
Of the 944 reports, 114 (12.1%) resulted in death, 241 (25.5%) required hospitalization, and 142 (15.0%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 944 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which NAPROXEN Alternatives Have Lower Intentional product misuse Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX