NYSTATIN and FUNGAL INFECTION

328 reports of this reaction

0.6% of all NYSTATIN reports

#78 most reported adverse reaction

Overview

FUNGAL INFECTION is the #78 most commonly reported adverse reaction for NYSTATIN, manufactured by Padagis US LLC. There are 328 FDA adverse event reports linking NYSTATIN to FUNGAL INFECTION. 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 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

FUNGAL INFECTION328 of 59,130 reports

FUNGAL INFECTION 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 fungal infection, the following adverse reactions have been reported for NYSTATIN:

Other Drugs Associated with FUNGAL INFECTION

The following drugs have also been linked to fungal infection in FDA adverse event reports:

CANAGLIFLOZINDAPAGLIFLOZINEMPAGLIFLOZINMICAFUNGIN SODIUMSALICYLIC ACID 2%

Frequently Asked Questions

Does NYSTATIN cause FUNGAL INFECTION?

FUNGAL INFECTION has been reported as an adverse event in 328 FDA reports for NYSTATIN. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is FUNGAL INFECTION with NYSTATIN?

FUNGAL INFECTION 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 FUNGAL INFECTION while taking NYSTATIN?

If you experience fungal infection 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.