CHLOROXYLENOL and ANGIOEDEMA

1 reports of this reaction

0.9% of all CHLOROXYLENOL reports

#17 most reported adverse reaction

Overview

ANGIOEDEMA is the #17 most commonly reported adverse reaction for CHLOROXYLENOL. There are 1 FDA adverse event reports linking CHLOROXYLENOL to ANGIOEDEMA. This represents approximately 0.9% of all 109 adverse event reports for this drug.

Patients taking CHLOROXYLENOL who experience angioedema 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

ANGIOEDEMA1 of 109 reports

ANGIOEDEMA is a less commonly reported adverse event for CHLOROXYLENOL, but still significant enough to appear in the safety profile.

Other Side Effects of CHLOROXYLENOL

In addition to angioedema, the following adverse reactions have been reported for CHLOROXYLENOL:

Other Drugs Associated with ANGIOEDEMA

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

ALTEPLASECEFUROXIME SODIUMINFLUENZINUMLISINOPRIL AND HYDROCHLOROTHIAZIDELISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETSMETHYL SALICYLATE

Frequently Asked Questions

Does CHLOROXYLENOL cause ANGIOEDEMA?

ANGIOEDEMA has been reported as an adverse event in 1 FDA reports for CHLOROXYLENOL. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is ANGIOEDEMA with CHLOROXYLENOL?

ANGIOEDEMA accounts for approximately 0.9% of all adverse event reports for CHLOROXYLENOL, making it a notable side effect.

What should I do if I experience ANGIOEDEMA while taking CHLOROXYLENOL?

If you experience angioedema while taking CHLOROXYLENOL, 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

CHLOROXYLENOL Full ProfileAll Drugs Causing ANGIOEDEMA
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.