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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does NAPROXEN Cause Poor quality product administered? 76 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Poor quality product administered have been filed in association with NAPROXEN (Naproxen Sodium). This represents 0.1% of all adverse event reports for NAPROXEN.

76
Reports of Poor quality product administered with NAPROXEN
0.1%
of all NAPROXEN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Poor quality product administered From NAPROXEN?

Of the 76 reports.

Is Poor quality product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 76 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 Poor quality product administered?

ONABOTULINUMTOXINA (495) ICOSAPENT ETHYL (452) MINOXIDIL (428) TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376) ADALIMUMAB (239) TESTOSTERONE CYPIONATE (235) SOMATROPIN (234) POLYETHYLENE GLYCOL 3350 (223) IBUPROFEN (222) INSULIN GLARGINE (133)

Which NAPROXEN Alternatives Have Lower Poor quality product administered Risk?

NAPROXEN vs NAPROXEN\NAPROXEN NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE NAPROXEN vs NAPROXEN\SUMATRIPTAN NAPROXEN vs NARATRIPTAN NAPROXEN vs NASONEX

Related Pages

NAPROXEN Full Profile All Poor quality product administered Reports All Drugs Causing Poor quality product administered NAPROXEN Demographics