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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 Adulterated product? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Adulterated product have been filed in association with NAPROXEN (Naproxen Sodium). This represents 0.0% of all adverse event reports for NAPROXEN.

6
Reports of Adulterated product with NAPROXEN
0.0%
of all NAPROXEN reports
4
Deaths
0
Hospitalizations

How Dangerous Is Adulterated product From NAPROXEN?

Of the 6 reports, 4 (66.7%) resulted in death.

Is Adulterated product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NAPROXEN. However, 6 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 Adulterated product?

LISDEXAMFETAMINE DIMESYLATE (31) THEOBROMINE (29) ACETAMINOPHEN (28) LIDOCAINE (28) COCAINE (27) CAFFEINE (24) CODEINE (23) THEOPHYLLINE (23) FENTANYL (22) MORPHINE (22)

Which NAPROXEN Alternatives Have Lower Adulterated product 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 Adulterated product Reports All Drugs Causing Adulterated product NAPROXEN Demographics