879 reports of this reaction
2.6% of all AZELASTINE reports
#6 most reported adverse reaction
NAUSEA is the #6 most commonly reported adverse reaction for AZELASTINE, manufactured by Amneal Pharmaceuticals LLC. There are 879 FDA adverse event reports linking AZELASTINE to NAUSEA. This represents approximately 2.6% of all 33,765 adverse event reports for this drug.
Patients taking AZELASTINE 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 AZELASTINE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for AZELASTINE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 879 FDA reports for AZELASTINE. 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 AZELASTINE, making it a notable side effect.
If you experience nausea while taking AZELASTINE, 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.