141 reports of this reaction
2.0% of all CROMOLYN SODIUM reports
#9 most reported adverse reaction
URTICARIA is the #9 most commonly reported adverse reaction for CROMOLYN SODIUM, manufactured by Prestige Brands Holdings, Inc.. There are 141 FDA adverse event reports linking CROMOLYN SODIUM to URTICARIA. This represents approximately 2.0% of all 7,214 adverse event reports for this drug.
Patients taking CROMOLYN SODIUM who experience urticaria should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
URTICARIA is a less commonly reported adverse event for CROMOLYN SODIUM, but still significant enough to appear in the safety profile.
In addition to urticaria, the following adverse reactions have been reported for CROMOLYN SODIUM:
The following drugs have also been linked to urticaria in FDA adverse event reports:
URTICARIA has been reported as an adverse event in 141 FDA reports for CROMOLYN SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
URTICARIA accounts for approximately 2.0% of all adverse event reports for CROMOLYN SODIUM, making it a notable side effect.
If you experience urticaria while taking CROMOLYN SODIUM, 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.