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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 Device use error? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device use error have been filed in association with NAPROXEN (Naproxen Sodium). This represents 0.0% of all adverse event reports for NAPROXEN.

5
Reports of Device use error with NAPROXEN
0.0%
of all NAPROXEN reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device use error From NAPROXEN?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Device use error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 5 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 Device use error?

PEGFILGRASTIM (6,001) ALBUTEROL (5,215) ALBIGLUTIDE (4,056) EVOLOCUMAB (4,002) SOMATROPIN (2,801) FLUTICASONE\SALMETEROL (1,749) FLUTICASONE (783) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766) ERENUMAB-AOOE (711) ETANERCEPT (665)

Which NAPROXEN Alternatives Have Lower Device use error 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 Device use error Reports All Drugs Causing Device use error NAPROXEN Demographics