118 reports of this reaction
2.6% of all FLUVOXAMINE MALEATE reports
#3 most reported adverse reaction
NAUSEA is the #3 most commonly reported adverse reaction for FLUVOXAMINE MALEATE, manufactured by ANI Pharmaceuticals, Inc.. There are 118 FDA adverse event reports linking FLUVOXAMINE MALEATE to NAUSEA. This represents approximately 2.6% of all 4,575 adverse event reports for this drug.
Patients taking FLUVOXAMINE MALEATE who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is a less commonly reported adverse event for FLUVOXAMINE MALEATE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for FLUVOXAMINE MALEATE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 118 FDA reports for FLUVOXAMINE MALEATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.6% of all adverse event reports for FLUVOXAMINE MALEATE, making it one of the most commonly reported side effect.
If you experience nausea while taking FLUVOXAMINE MALEATE, 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.