28 reports of this reaction
2.1% of all IMIPRAMINE HYDROCHLORIDE reports
#7 most reported adverse reaction
DEPRESSION is the #7 most commonly reported adverse reaction for IMIPRAMINE HYDROCHLORIDE, manufactured by Key Therapeutics. There are 28 FDA adverse event reports linking IMIPRAMINE HYDROCHLORIDE to DEPRESSION. This represents approximately 2.1% of all 1,335 adverse event reports for this drug.
Patients taking IMIPRAMINE HYDROCHLORIDE who experience depression should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEPRESSION is a less commonly reported adverse event for IMIPRAMINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to depression, the following adverse reactions have been reported for IMIPRAMINE HYDROCHLORIDE:
The following drugs have also been linked to depression in FDA adverse event reports:
DEPRESSION has been reported as an adverse event in 28 FDA reports for IMIPRAMINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEPRESSION accounts for approximately 2.1% of all adverse event reports for IMIPRAMINE HYDROCHLORIDE, making it a notable side effect.
If you experience depression while taking IMIPRAMINE 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.