275 reports of this reaction
1.1% of all ESKETAMINE HYDROCHLORIDE reports
#20 most reported adverse reaction
ADVERSE EVENT is the #20 most commonly reported adverse reaction for ESKETAMINE HYDROCHLORIDE, manufactured by Janssen Pharmaceuticals Inc.. There are 275 FDA adverse event reports linking ESKETAMINE HYDROCHLORIDE to ADVERSE EVENT. This represents approximately 1.1% of all 24,470 adverse event reports for this drug.
Patients taking ESKETAMINE HYDROCHLORIDE who experience adverse event should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ADVERSE EVENT is a less commonly reported adverse event for ESKETAMINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to adverse event, the following adverse reactions have been reported for ESKETAMINE HYDROCHLORIDE:
The following drugs have also been linked to adverse event in FDA adverse event reports:
ADVERSE EVENT has been reported as an adverse event in 275 FDA reports for ESKETAMINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ADVERSE EVENT accounts for approximately 1.1% of all adverse event reports for ESKETAMINE HYDROCHLORIDE, making it a notable side effect.
If you experience adverse event while taking ESKETAMINE 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.