NYSTATIN and CHRONIC OBSTRUCTIVE PULMONARY DISEASE

354 reports of this reaction

0.6% of all NYSTATIN reports

#65 most reported adverse reaction

Overview

CHRONIC OBSTRUCTIVE PULMONARY DISEASE is the #65 most commonly reported adverse reaction for NYSTATIN, manufactured by Padagis US LLC. There are 354 FDA adverse event reports linking NYSTATIN to CHRONIC OBSTRUCTIVE PULMONARY DISEASE. This represents approximately 0.6% of all 59,130 adverse event reports for this drug.

NYSTATIN has an overall safety score of 82 out of 100. Patients taking NYSTATIN who experience chronic obstructive pulmonary disease 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

CHRONIC OBSTRUCTIVE PULMONARY DISEASE354 of 59,130 reports

CHRONIC OBSTRUCTIVE PULMONARY DISEASE is a less commonly reported adverse event for NYSTATIN, but still significant enough to appear in the safety profile.

Other Side Effects of NYSTATIN

In addition to chronic obstructive pulmonary disease, the following adverse reactions have been reported for NYSTATIN:

Frequently Asked Questions

Does NYSTATIN cause CHRONIC OBSTRUCTIVE PULMONARY DISEASE?

CHRONIC OBSTRUCTIVE PULMONARY DISEASE has been reported as an adverse event in 354 FDA reports for NYSTATIN. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is CHRONIC OBSTRUCTIVE PULMONARY DISEASE with NYSTATIN?

CHRONIC OBSTRUCTIVE PULMONARY DISEASE accounts for approximately 0.6% of all adverse event reports for NYSTATIN, making it a notable side effect.

What should I do if I experience CHRONIC OBSTRUCTIVE PULMONARY DISEASE while taking NYSTATIN?

If you experience chronic obstructive pulmonary disease while taking NYSTATIN, 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.

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.