754 reports of this reaction
2.1% of all PRAMIPEXOLE reports
#7 most reported adverse reaction
HALLUCINATION is the #7 most commonly reported adverse reaction for PRAMIPEXOLE, manufactured by Camber Pharmaceuticals, Inc.. There are 754 FDA adverse event reports linking PRAMIPEXOLE to HALLUCINATION. This represents approximately 2.1% of all 35,207 adverse event reports for this drug.
Patients taking PRAMIPEXOLE who experience hallucination should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HALLUCINATION is a less commonly reported adverse event for PRAMIPEXOLE, but still significant enough to appear in the safety profile.
In addition to hallucination, the following adverse reactions have been reported for PRAMIPEXOLE:
The following drugs have also been linked to hallucination in FDA adverse event reports:
HALLUCINATION has been reported as an adverse event in 754 FDA reports for PRAMIPEXOLE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HALLUCINATION accounts for approximately 2.1% of all adverse event reports for PRAMIPEXOLE, making it a notable side effect.
If you experience hallucination 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.