221 reports of this reaction
2.3% of all NUSINERSEN reports
#10 most reported adverse reaction
SCOLIOSIS is the #10 most commonly reported adverse reaction for NUSINERSEN. There are 221 FDA adverse event reports linking NUSINERSEN to SCOLIOSIS. This represents approximately 2.3% of all 9,682 adverse event reports for this drug.
Patients taking NUSINERSEN who experience scoliosis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SCOLIOSIS is a less commonly reported adverse event for NUSINERSEN, but still significant enough to appear in the safety profile.
In addition to scoliosis, the following adverse reactions have been reported for NUSINERSEN:
SCOLIOSIS has been reported as an adverse event in 221 FDA reports for NUSINERSEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
SCOLIOSIS accounts for approximately 2.3% of all adverse event reports for NUSINERSEN, making it a notable side effect.
If you experience scoliosis while taking NUSINERSEN, 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.