Does NAPROXEN Cause Incorrect product administration duration? 499 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 499 reports of Incorrect product administration duration have been filed in association with NAPROXEN (Naproxen Sodium). This represents 1.0% of all adverse event reports for NAPROXEN.
499
Reports of Incorrect product administration duration with NAPROXEN
1.0%
of all NAPROXEN reports
61
Deaths
88
Hospitalizations
How Dangerous Is Incorrect product administration duration From NAPROXEN?
Of the 499 reports, 61 (12.2%) resulted in death, 88 (17.6%) required hospitalization, and 62 (12.4%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 499 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 administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
ALENDRONATE (287)
Which NAPROXEN Alternatives Have Lower Incorrect product administration duration Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX