Does NAPROXEN Cause Suspected product quality issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Suspected product quality issue have been filed in association with NAPROXEN (Naproxen Sodium). This represents 0.0% of all adverse event reports for NAPROXEN.
7
Reports of Suspected product quality issue with NAPROXEN
0.0%
of all NAPROXEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Suspected product quality issue From NAPROXEN?
Of the 7 reports.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 7 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 Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
Which NAPROXEN Alternatives Have Lower Suspected product quality issue Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX