279 reports of this reaction
2.1% of all GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE reports
#10 most reported adverse reaction
VOMITING is the #10 most commonly reported adverse reaction for GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE, manufactured by RB Health (US) LLC. There are 279 FDA adverse event reports linking GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE to VOMITING. This represents approximately 2.1% of all 13,133 adverse event reports for this drug.
Patients taking GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE who experience vomiting should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
VOMITING is a less commonly reported adverse event for GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE, but still significant enough to appear in the safety profile.
In addition to vomiting, the following adverse reactions have been reported for GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE:
The following drugs have also been linked to vomiting in FDA adverse event reports:
VOMITING has been reported as an adverse event in 279 FDA reports for GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
VOMITING accounts for approximately 2.1% of all adverse event reports for GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE, making it a notable side effect.
If you experience vomiting while taking GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE, 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.