COUGH is the #7 most commonly reported adverse reaction for GUAIFENESIN, manufactured by RB Health (US) LLC. There are 1,557 FDA adverse event reports linking GUAIFENESIN to COUGH. This represents approximately 2.5% of all 61,553 adverse event reports for this drug.
Patients taking GUAIFENESIN 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
COUGH1,557 of 61,553 reports
COUGH is a less commonly reported adverse event for GUAIFENESIN, but still significant enough to appear in the safety profile.
Other Side Effects of GUAIFENESIN
In addition to cough, the following adverse reactions have been reported for GUAIFENESIN:
COUGH has been reported as an adverse event in 1,557 FDA reports for GUAIFENESIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is COUGH with GUAIFENESIN?
COUGH accounts for approximately 2.5% of all adverse event reports for GUAIFENESIN, making it a notable side effect.
What should I do if I experience COUGH while taking GUAIFENESIN?
If you experience cough while taking GUAIFENESIN, 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.