29 reports of this reaction
2.2% of all IMIPRAMINE HYDROCHLORIDE reports
#5 most reported adverse reaction
HYPERTENSION is the #5 most commonly reported adverse reaction for IMIPRAMINE HYDROCHLORIDE, manufactured by Key Therapeutics. There are 29 FDA adverse event reports linking IMIPRAMINE HYDROCHLORIDE to HYPERTENSION. This represents approximately 2.2% of all 1,335 adverse event reports for this drug.
Patients taking IMIPRAMINE HYDROCHLORIDE who experience hypertension should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPERTENSION is a less commonly reported adverse event for IMIPRAMINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to hypertension, the following adverse reactions have been reported for IMIPRAMINE HYDROCHLORIDE:
The following drugs have also been linked to hypertension in FDA adverse event reports:
HYPERTENSION has been reported as an adverse event in 29 FDA reports for IMIPRAMINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERTENSION accounts for approximately 2.2% of all adverse event reports for IMIPRAMINE HYDROCHLORIDE, making it a notable side effect.
If you experience hypertension 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.