6,825 reports of this reaction
3.3% of all CITALOPRAM HYDROBROMIDE reports
#1 most reported adverse reaction
FATIGUE is the #1 most commonly reported adverse reaction for CITALOPRAM HYDROBROMIDE, manufactured by Aurobindo Pharma Limited. There are 6,825 FDA adverse event reports linking CITALOPRAM HYDROBROMIDE to FATIGUE. This represents approximately 3.3% of all 209,370 adverse event reports for this drug.
Patients taking CITALOPRAM HYDROBROMIDE 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 moderately reported among CITALOPRAM HYDROBROMIDE users, representing a notable but not dominant share of adverse events.
In addition to fatigue, the following adverse reactions have been reported for CITALOPRAM HYDROBROMIDE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 6,825 FDA reports for CITALOPRAM HYDROBROMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 3.3% of all adverse event reports for CITALOPRAM HYDROBROMIDE, making it one of the most commonly reported side effect.
If you experience fatigue while taking CITALOPRAM HYDROBROMIDE, 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.