140 reports of this reaction
1.9% of all HYDROXYZINE PAMOATE reports
#11 most reported adverse reaction
OFF LABEL USE is the #11 most commonly reported adverse reaction for HYDROXYZINE PAMOATE, manufactured by Amneal Pharmaceuticals of New York LLC. There are 140 FDA adverse event reports linking HYDROXYZINE PAMOATE to OFF LABEL USE. This represents approximately 1.9% of all 7,494 adverse event reports for this drug.
Patients taking HYDROXYZINE PAMOATE who experience off label use should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OFF LABEL USE is a less commonly reported adverse event for HYDROXYZINE PAMOATE, but still significant enough to appear in the safety profile.
In addition to off label use, the following adverse reactions have been reported for HYDROXYZINE PAMOATE:
The following drugs have also been linked to off label use in FDA adverse event reports:
OFF LABEL USE has been reported as an adverse event in 140 FDA reports for HYDROXYZINE PAMOATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 1.9% of all adverse event reports for HYDROXYZINE PAMOATE, making it a notable side effect.
If you experience off label use while taking HYDROXYZINE PAMOATE, 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.