FLUTICASONE FUROATE and COUGH

Overview

COUGH is the #5 most commonly reported adverse reaction for FLUTICASONE FUROATE, manufactured by GlaxoSmithKline LLC. There are 871 FDA adverse event reports linking FLUTICASONE FUROATE to COUGH. This represents approximately 2.4% of all 35,585 adverse event reports for this drug.

Patients taking FLUTICASONE FUROATE 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 FLUTICASONE FUROATE, but still significant enough to appear in the safety profile.

Other Side Effects of FLUTICASONE FUROATE

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

• DRUG INEFFECTIVE — 1,994 reports
• DYSPNOEA — 1,498 reports
• ASTHMA — 1,252 reports
• OFF LABEL USE — 984 reports
• WHEEZING — 852 reports
• THERAPEUTIC PRODUCT EFFECT INCOMPLETE — 759 reports
• PRODUCT USE IN UNAPPROVED INDICATION — 690 reports
• HEADACHE — 668 reports
• NAUSEA — 668 reports
• PAIN — 653 reports

Other Drugs Associated with COUGH

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

Does FLUTICASONE FUROATE cause COUGH?

COUGH has been reported as an adverse event in 871 FDA reports for FLUTICASONE FUROATE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is COUGH with FLUTICASONE FUROATE?

COUGH accounts for approximately 2.4% of all adverse event reports for FLUTICASONE FUROATE, making it a notable side effect.

What should I do if I experience COUGH while taking FLUTICASONE FUROATE?

If you experience cough while taking FLUTICASONE FUROATE, 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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