Does NAPROXEN Cause Wrong technique in product usage process? 531 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 531 reports of Wrong technique in product usage process have been filed in association with NAPROXEN (Naproxen Sodium). This represents 1.0% of all adverse event reports for NAPROXEN.
531
Reports of Wrong technique in product usage process with NAPROXEN
1.0%
of all NAPROXEN reports
3
Deaths
20
Hospitalizations
How Dangerous Is Wrong technique in product usage process From NAPROXEN?
Of the 531 reports, 3 (0.6%) resulted in death, 20 (3.8%) required hospitalization, and 4 (0.8%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 531 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which NAPROXEN Alternatives Have Lower Wrong technique in product usage process Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX