8,206 reports of this reaction
3.1% of all CITALOPRAM reports
#2 most reported adverse reaction
NAUSEA is the #2 most commonly reported adverse reaction for CITALOPRAM, manufactured by Aurobindo Pharma Limited. There are 8,206 FDA adverse event reports linking CITALOPRAM to NAUSEA. This represents approximately 3.1% of all 266,799 adverse event reports for this drug.
Patients taking CITALOPRAM 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 moderately reported among CITALOPRAM users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for CITALOPRAM:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 8,206 FDA reports for CITALOPRAM. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.1% of all adverse event reports for CITALOPRAM, making it one of the most commonly reported side effect.
If you experience nausea while taking CITALOPRAM, 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.