Does NAPROXEN Cause Product quality issue? 666 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 666 reports of Product quality issue have been filed in association with NAPROXEN (Naproxen Sodium). This represents 1.3% of all adverse event reports for NAPROXEN.
666
Reports of Product quality issue with NAPROXEN
1.3%
of all NAPROXEN reports
500
Deaths
429
Hospitalizations
How Dangerous Is Product quality issue From NAPROXEN?
Of the 666 reports, 500 (75.1%) resulted in death, 429 (64.4%) required hospitalization, and 437 (65.6%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 666 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which NAPROXEN Alternatives Have Lower Product quality issue Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX