Does NAPROXEN Cause Incorrect product storage? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Incorrect product storage have been filed in association with NAPROXEN (Naproxen Sodium). This represents 0.0% of all adverse event reports for NAPROXEN.
13
Reports of Incorrect product storage with NAPROXEN
0.0%
of all NAPROXEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From NAPROXEN?
Of the 13 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 13 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which NAPROXEN Alternatives Have Lower Incorrect product storage Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX