Does NAPROXEN Cause Expired product administered? 1,305 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,305 reports of Expired product administered have been filed in association with NAPROXEN (Naproxen Sodium). This represents 2.5% of all adverse event reports for NAPROXEN.
1,305
Reports of Expired product administered with NAPROXEN
2.5%
of all NAPROXEN reports
1
Deaths
10
Hospitalizations
How Dangerous Is Expired product administered From NAPROXEN?
Of the 1,305 reports, 1 (0.1%) resulted in death, 10 (0.8%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 1,305 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
NICOTINE (704)
Which NAPROXEN Alternatives Have Lower Expired product administered Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX