PYRANTEL PAMOATE and ANAL FUNGAL INFECTION

1 reports of this reaction

1.2% of all PYRANTEL PAMOATE reports

#10 most reported adverse reaction

Overview

ANAL FUNGAL INFECTION is the #10 most commonly reported adverse reaction for PYRANTEL PAMOATE, manufactured by REESE PHARMACEUTICAL CO.. There are 1 FDA adverse event reports linking PYRANTEL PAMOATE to ANAL FUNGAL INFECTION. This represents approximately 1.2% of all 83 adverse event reports for this drug.

Patients taking PYRANTEL PAMOATE who experience anal fungal infection should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

ANAL FUNGAL INFECTION1 of 83 reports

ANAL FUNGAL INFECTION is a less commonly reported adverse event for PYRANTEL PAMOATE, but still significant enough to appear in the safety profile.

Other Side Effects of PYRANTEL PAMOATE

In addition to anal fungal infection, the following adverse reactions have been reported for PYRANTEL PAMOATE:

Frequently Asked Questions

Does PYRANTEL PAMOATE cause ANAL FUNGAL INFECTION?

ANAL FUNGAL INFECTION 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.

How common is ANAL FUNGAL INFECTION with PYRANTEL PAMOATE?

ANAL FUNGAL INFECTION accounts for approximately 1.2% of all adverse event reports for PYRANTEL PAMOATE, making it a notable side effect.

What should I do if I experience ANAL FUNGAL INFECTION while taking PYRANTEL PAMOATE?

If you experience anal fungal infection 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.

Related Pages

PYRANTEL PAMOATE Full ProfileAll Drugs Causing ANAL FUNGAL INFECTIONREESE PHARMACEUTICAL CO. Drugs
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.