BUDESONIDE and COUGH

Overview

COUGH is the #6 most commonly reported adverse reaction for BUDESONIDE, manufactured by H2-Pharma LLC. There are 3,164 FDA adverse event reports linking BUDESONIDE to COUGH. This represents approximately 2.3% of all 134,730 adverse event reports for this drug.

Patients taking BUDESONIDE 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

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

Other Side Effects of BUDESONIDE

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

• DYSPNOEA — 6,362 reports
• DRUG INEFFECTIVE — 6,019 reports
• OFF LABEL USE — 5,694 reports
• ASTHMA — 4,696 reports
• FATIGUE — 3,354 reports
• HEADACHE — 2,978 reports
• DIARRHOEA — 2,696 reports
• CONDITION AGGRAVATED — 2,695 reports
• NAUSEA — 2,620 reports
• PNEUMONIA — 2,556 reports

Other Drugs Associated with COUGH

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

Does BUDESONIDE cause COUGH?

COUGH has been reported as an adverse event in 3,164 FDA reports for BUDESONIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is COUGH with BUDESONIDE?

COUGH accounts for approximately 2.3% of all adverse event reports for BUDESONIDE, making it a notable side effect.

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

If you experience cough while taking BUDESONIDE, 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.

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