771 reports of this reaction
2.2% of all AMANTADINE reports
#9 most reported adverse reaction
TREMOR is the #9 most commonly reported adverse reaction for AMANTADINE, manufactured by Adamas Pharma, LLC. There are 771 FDA adverse event reports linking AMANTADINE to TREMOR. This represents approximately 2.2% of all 34,976 adverse event reports for this drug.
Patients taking AMANTADINE who experience tremor should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
TREMOR is a less commonly reported adverse event for AMANTADINE, but still significant enough to appear in the safety profile.
In addition to tremor, the following adverse reactions have been reported for AMANTADINE:
The following drugs have also been linked to tremor in FDA adverse event reports:
TREMOR has been reported as an adverse event in 771 FDA reports for AMANTADINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
TREMOR accounts for approximately 2.2% of all adverse event reports for AMANTADINE, making it a notable side effect.
If you experience tremor while taking AMANTADINE, 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.