1 reports of this reaction
1.2% of all PYRANTEL PAMOATE reports
#9 most reported adverse reaction
ACCIDENTAL OVERDOSE is the #9 most commonly reported adverse reaction for PYRANTEL PAMOATE, manufactured by REESE PHARMACEUTICAL CO.. There are 1 FDA adverse event reports linking PYRANTEL PAMOATE to ACCIDENTAL OVERDOSE. This represents approximately 1.2% of all 83 adverse event reports for this drug.
Patients taking PYRANTEL PAMOATE who experience accidental overdose should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ACCIDENTAL OVERDOSE is a less commonly reported adverse event for PYRANTEL PAMOATE, but still significant enough to appear in the safety profile.
In addition to accidental overdose, the following adverse reactions have been reported for PYRANTEL PAMOATE:
The following drugs have also been linked to accidental overdose in FDA adverse event reports:
ACCIDENTAL OVERDOSE has been reported as an adverse event in 1 FDA reports for PYRANTEL PAMOATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ACCIDENTAL OVERDOSE accounts for approximately 1.2% of all adverse event reports for PYRANTEL PAMOATE, making it a notable side effect.
If you experience accidental overdose 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.