PERPHENAZINE and EUPHORIC MOOD

153 reports of this reaction

2.0% of all PERPHENAZINE reports

#9 most reported adverse reaction

Overview

EUPHORIC MOOD is the #9 most commonly reported adverse reaction for PERPHENAZINE, manufactured by Actavis Pharma, Inc.. There are 153 FDA adverse event reports linking PERPHENAZINE to EUPHORIC MOOD. This represents approximately 2.0% of all 7,483 adverse event reports for this drug.

Patients taking PERPHENAZINE who experience euphoric mood should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

EUPHORIC MOOD153 of 7,483 reports

EUPHORIC MOOD is a less commonly reported adverse event for PERPHENAZINE, but still significant enough to appear in the safety profile.

Other Side Effects of PERPHENAZINE

In addition to euphoric mood, the following adverse reactions have been reported for PERPHENAZINE:

Other Drugs Associated with EUPHORIC MOOD

The following drugs have also been linked to euphoric mood in FDA adverse event reports:

LOXAPINE

Frequently Asked Questions

Does PERPHENAZINE cause EUPHORIC MOOD?

EUPHORIC MOOD has been reported as an adverse event in 153 FDA reports for PERPHENAZINE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is EUPHORIC MOOD with PERPHENAZINE?

EUPHORIC MOOD accounts for approximately 2.0% of all adverse event reports for PERPHENAZINE, making it a notable side effect.

What should I do if I experience EUPHORIC MOOD while taking PERPHENAZINE?

If you experience euphoric mood while taking PERPHENAZINE, 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.

Related Pages

PERPHENAZINE Full ProfileAll Drugs Causing EUPHORIC MOODActavis Pharma, Inc. Drugs
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.