4,622 reports of this reaction
1.9% of all PSEUDOEPHEDRINE HCL reports
#8 most reported adverse reaction
GLOSSODYNIA is the #8 most commonly reported adverse reaction for PSEUDOEPHEDRINE HCL, manufactured by Major Pharmaceuticals. There are 4,622 FDA adverse event reports linking PSEUDOEPHEDRINE HCL to GLOSSODYNIA. This represents approximately 1.9% of all 242,486 adverse event reports for this drug.
Patients taking PSEUDOEPHEDRINE HCL who experience glossodynia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
GLOSSODYNIA is a less commonly reported adverse event for PSEUDOEPHEDRINE HCL, but still significant enough to appear in the safety profile.
In addition to glossodynia, the following adverse reactions have been reported for PSEUDOEPHEDRINE HCL:
The following drugs have also been linked to glossodynia in FDA adverse event reports:
GLOSSODYNIA has been reported as an adverse event in 4,622 FDA reports for PSEUDOEPHEDRINE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.
GLOSSODYNIA accounts for approximately 1.9% of all adverse event reports for PSEUDOEPHEDRINE HCL, making it a notable side effect.
If you experience glossodynia while taking PSEUDOEPHEDRINE HCL, 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.