17 reports of this reaction
20.5% of all PYRANTEL PAMOATE reports
#1 most reported adverse reaction
ADVERSE EVENT is the #1 most commonly reported adverse reaction for PYRANTEL PAMOATE, manufactured by REESE PHARMACEUTICAL CO.. There are 17 FDA adverse event reports linking PYRANTEL PAMOATE to ADVERSE EVENT. This represents approximately 20.5% of all 83 adverse event reports for this drug.
Patients taking PYRANTEL PAMOATE who experience adverse event should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ADVERSE EVENT is a frequently reported adverse event for PYRANTEL PAMOATE, accounting for a significant proportion of all reports.
In addition to adverse event, the following adverse reactions have been reported for PYRANTEL PAMOATE:
The following drugs have also been linked to adverse event in FDA adverse event reports:
ADVERSE EVENT has been reported as an adverse event in 17 FDA reports for PYRANTEL PAMOATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ADVERSE EVENT accounts for approximately 20.5% of all adverse event reports for PYRANTEL PAMOATE, making it one of the most commonly reported side effect.
If you experience adverse event while taking PYRANTEL 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.