41 reports of this reaction
1.7% of all DANTROLENE SODIUM reports
#13 most reported adverse reaction
CONVULSION is the #13 most commonly reported adverse reaction for DANTROLENE SODIUM, manufactured by Endo USA, Inc.. There are 41 FDA adverse event reports linking DANTROLENE SODIUM to CONVULSION. This represents approximately 1.7% of all 2,376 adverse event reports for this drug.
Patients taking DANTROLENE SODIUM who experience convulsion should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CONVULSION is a less commonly reported adverse event for DANTROLENE SODIUM, but still significant enough to appear in the safety profile.
In addition to convulsion, the following adverse reactions have been reported for DANTROLENE SODIUM:
The following drugs have also been linked to convulsion in FDA adverse event reports:
CONVULSION has been reported as an adverse event in 41 FDA reports for DANTROLENE SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
CONVULSION accounts for approximately 1.7% of all adverse event reports for DANTROLENE SODIUM, making it a notable side effect.
If you experience convulsion while taking DANTROLENE SODIUM, 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.