102 reports of this reaction
1.5% of all FINGOLIMOD reports
#12 most reported adverse reaction
HYPOAESTHESIA is the #12 most commonly reported adverse reaction for FINGOLIMOD, manufactured by Apotex Corp.. There are 102 FDA adverse event reports linking FINGOLIMOD to HYPOAESTHESIA. This represents approximately 1.5% of all 6,602 adverse event reports for this drug.
Patients taking FINGOLIMOD who experience hypoaesthesia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPOAESTHESIA is a less commonly reported adverse event for FINGOLIMOD, but still significant enough to appear in the safety profile.
In addition to hypoaesthesia, the following adverse reactions have been reported for FINGOLIMOD:
The following drugs have also been linked to hypoaesthesia in FDA adverse event reports:
HYPOAESTHESIA has been reported as an adverse event in 102 FDA reports for FINGOLIMOD. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOAESTHESIA accounts for approximately 1.5% of all adverse event reports for FINGOLIMOD, making it a notable side effect.
If you experience hypoaesthesia while taking FINGOLIMOD, 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.