2,055 reports of this reaction
4.9% of all LURASIDONE HYDROCHLORIDE reports
#1 most reported adverse reaction
OFF LABEL USE is the #1 most commonly reported adverse reaction for LURASIDONE HYDROCHLORIDE, manufactured by Sumitomo Pharma America, Inc.. There are 2,055 FDA adverse event reports linking LURASIDONE HYDROCHLORIDE to OFF LABEL USE. This represents approximately 4.9% of all 41,710 adverse event reports for this drug.
Patients taking LURASIDONE HYDROCHLORIDE who experience off label use should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OFF LABEL USE is moderately reported among LURASIDONE HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to off label use, the following adverse reactions have been reported for LURASIDONE HYDROCHLORIDE:
The following drugs have also been linked to off label use in FDA adverse event reports:
OFF LABEL USE has been reported as an adverse event in 2,055 FDA reports for LURASIDONE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 4.9% of all adverse event reports for LURASIDONE HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience off label use while taking LURASIDONE 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.