Does NAPROXEN Cause Recalled product administered? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Recalled product administered have been filed in association with NAPROXEN (Naproxen Sodium). This represents 0.0% of all adverse event reports for NAPROXEN.
5
Reports of Recalled product administered with NAPROXEN
0.0%
of all NAPROXEN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Recalled product administered From NAPROXEN?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Recalled product administered 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which NAPROXEN Alternatives Have Lower Recalled product administered Risk?
NAPROXEN vs NAPROXEN\NAPROXEN
NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN vs NARATRIPTAN
NAPROXEN vs NASONEX