Does NAPROXEN\NAPROXEN Cause Adverse event? 70 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 70 reports of Adverse event have been filed in association with NAPROXEN\NAPROXEN. This represents 6.1% of all adverse event reports for NAPROXEN\NAPROXEN.
70
Reports of Adverse event with NAPROXEN\NAPROXEN
6.1%
of all NAPROXEN\NAPROXEN reports
42
Deaths
59
Hospitalizations
How Dangerous Is Adverse event From NAPROXEN\NAPROXEN?
Of the 70 reports, 42 (60.0%) resulted in death, 59 (84.3%) required hospitalization, and 66 (94.3%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NAPROXEN\NAPROXEN. However, 70 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which NAPROXEN\NAPROXEN Alternatives Have Lower Adverse event Risk?
NAPROXEN\NAPROXEN vs NAPROXEN\PSEUDOEPHEDRINE
NAPROXEN\NAPROXEN vs NAPROXEN\SUMATRIPTAN
NAPROXEN\NAPROXEN vs NARATRIPTAN
NAPROXEN\NAPROXEN vs NASONEX
NAPROXEN\NAPROXEN vs NATALIZUMAB