Does NAPROXEN\NAPROXEN Cause Product quality issue? 82 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 82 reports of Product quality issue have been filed in association with NAPROXEN\NAPROXEN. This represents 7.1% of all adverse event reports for NAPROXEN\NAPROXEN.
82
Reports of Product quality issue with NAPROXEN\NAPROXEN
7.1%
of all NAPROXEN\NAPROXEN reports
73
Deaths
77
Hospitalizations
How Dangerous Is Product quality issue From NAPROXEN\NAPROXEN?
Of the 82 reports, 73 (89.0%) resulted in death, 77 (93.9%) required hospitalization, and 78 (95.1%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN\NAPROXEN. However, 82 reports have been filed with the FAERS database.
What Other Side Effects Does NAPROXEN\NAPROXEN Cause?
Fatigue (502)
Mobility decreased (467)
Off label use (462)
Fibromyalgia (456)
Folliculitis (449)
Joint swelling (448)
Psoriatic arthropathy (445)
Glossodynia (434)
General physical health deterioration (433)
Hand deformity (431)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which NAPROXEN\NAPROXEN Alternatives Have Lower Product quality issue Risk?
NAPROXEN\NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN\NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN\NAPROXEN vs NARATRIPTAN
NAPROXEN\NAPROXEN vs NASONEX
NAPROXEN\NAPROXEN vs NATALIZUMAB