8,006 reports of this reaction
9.4% of all NAPROXEN SODIUM TABLET reports
#1 most reported adverse reaction
DRUG INEFFECTIVE is the #1 most commonly reported adverse reaction for NAPROXEN SODIUM TABLET, manufactured by Bayer HealthCare LLC.. There are 8,006 FDA adverse event reports linking NAPROXEN SODIUM TABLET to DRUG INEFFECTIVE. This represents approximately 9.4% of all 85,607 adverse event reports for this drug.
NAPROXEN SODIUM TABLET has an overall safety score of 78 out of 100. Patients taking NAPROXEN SODIUM TABLET who experience drug ineffective should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRUG INEFFECTIVE is moderately reported among NAPROXEN SODIUM TABLET users, representing a notable but not dominant share of adverse events.
In addition to drug ineffective, the following adverse reactions have been reported for NAPROXEN SODIUM TABLET:
The following drugs have also been linked to drug ineffective in FDA adverse event reports:
DRUG INEFFECTIVE has been reported as an adverse event in 8,006 FDA reports for NAPROXEN SODIUM TABLET. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG INEFFECTIVE accounts for approximately 9.4% of all adverse event reports for NAPROXEN SODIUM TABLET, making it one of the most commonly reported side effect.
If you experience drug ineffective while taking NAPROXEN SODIUM TABLET, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.