85 reports of this reaction
1.9% of all FLUVOXAMINE MALEATE reports
#10 most reported adverse reaction
FATIGUE is the #10 most commonly reported adverse reaction for FLUVOXAMINE MALEATE, manufactured by ANI Pharmaceuticals, Inc.. There are 85 FDA adverse event reports linking FLUVOXAMINE MALEATE to FATIGUE. This represents approximately 1.9% of all 4,575 adverse event reports for this drug.
Patients taking FLUVOXAMINE MALEATE who experience fatigue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FATIGUE is a less commonly reported adverse event for FLUVOXAMINE MALEATE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for FLUVOXAMINE MALEATE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 85 FDA reports for FLUVOXAMINE MALEATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 1.9% of all adverse event reports for FLUVOXAMINE MALEATE, making it a notable side effect.
If you experience fatigue 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.