Symbicort and COUGH

7,830 reports of this reaction

3.3% of all Symbicort reports

#3 most reported adverse reaction

Overview

COUGH is the #3 most commonly reported adverse reaction for Symbicort, manufactured by AstraZeneca Pharmaceuticals LP. There are 7,830 FDA adverse event reports linking Symbicort to COUGH. This represents approximately 3.3% of all 240,442 adverse event reports for this drug.

Patients taking Symbicort who experience cough 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

COUGH7,830 of 240,442 reports

COUGH is moderately reported among Symbicort users, representing a notable but not dominant share of adverse events.

Other Side Effects of Symbicort

In addition to cough, the following adverse reactions have been reported for Symbicort:

Frequently Asked Questions

Does Symbicort cause COUGH?

COUGH has been reported as an adverse event in 7,830 FDA reports for Symbicort. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is COUGH with Symbicort?

COUGH accounts for approximately 3.3% of all adverse event reports for Symbicort, making it one of the most commonly reported side effect.

What should I do if I experience COUGH while taking Symbicort?

If you experience cough while taking Symbicort, 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.