582 reports of this reaction
3.0% of all DESLORATADINE reports
#3 most reported adverse reaction
NAUSEA is the #3 most commonly reported adverse reaction for DESLORATADINE, manufactured by Organon LLC. There are 582 FDA adverse event reports linking DESLORATADINE to NAUSEA. This represents approximately 3.0% of all 19,228 adverse event reports for this drug.
Patients taking DESLORATADINE 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 DESLORATADINE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for DESLORATADINE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 582 FDA reports for DESLORATADINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.0% of all adverse event reports for DESLORATADINE, making it one of the most commonly reported side effect.
If you experience nausea while taking DESLORATADINE, 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.