710 reports of this reaction
2.0% of all PRAMIPEXOLE reports
#10 most reported adverse reaction
DYSPNOEA is the #10 most commonly reported adverse reaction for PRAMIPEXOLE, manufactured by Camber Pharmaceuticals, Inc.. There are 710 FDA adverse event reports linking PRAMIPEXOLE to DYSPNOEA. This represents approximately 2.0% of all 35,207 adverse event reports for this drug.
Patients taking PRAMIPEXOLE who experience dyspnoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSPNOEA is a less commonly reported adverse event for PRAMIPEXOLE, but still significant enough to appear in the safety profile.
In addition to dyspnoea, the following adverse reactions have been reported for PRAMIPEXOLE:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 710 FDA reports for PRAMIPEXOLE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 2.0% of all adverse event reports for PRAMIPEXOLE, making it a notable side effect.
If you experience dyspnoea while taking PRAMIPEXOLE, 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.