573 reports of this reaction
5.0% of all OZANIMOD HYDROCHLORIDE reports
#2 most reported adverse reaction
MULTIPLE SCLEROSIS RELAPSE is the #2 most commonly reported adverse reaction for OZANIMOD HYDROCHLORIDE, manufactured by Celgene Corporation. There are 573 FDA adverse event reports linking OZANIMOD HYDROCHLORIDE to MULTIPLE SCLEROSIS RELAPSE. This represents approximately 5.0% of all 11,558 adverse event reports for this drug.
Patients taking OZANIMOD HYDROCHLORIDE who experience multiple sclerosis relapse should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MULTIPLE SCLEROSIS RELAPSE is moderately reported among OZANIMOD HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to multiple sclerosis relapse, the following adverse reactions have been reported for OZANIMOD HYDROCHLORIDE:
The following drugs have also been linked to multiple sclerosis relapse in FDA adverse event reports:
MULTIPLE SCLEROSIS RELAPSE has been reported as an adverse event in 573 FDA reports for OZANIMOD HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MULTIPLE SCLEROSIS RELAPSE accounts for approximately 5.0% of all adverse event reports for OZANIMOD HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience multiple sclerosis relapse while taking OZANIMOD HYDROCHLORIDE, 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.