PURIFIED WATER and DEPRESSED MOOD

2 reports of this reaction

1.5% of all PURIFIED WATER reports

#10 most reported adverse reaction

Overview

DEPRESSED MOOD is the #10 most commonly reported adverse reaction for PURIFIED WATER, manufactured by McKesson. There are 2 FDA adverse event reports linking PURIFIED WATER to DEPRESSED MOOD. This represents approximately 1.5% of all 130 adverse event reports for this drug.

Patients taking PURIFIED WATER who experience depressed 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

DEPRESSED MOOD2 of 130 reports

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

Other Side Effects of PURIFIED WATER

In addition to depressed mood, the following adverse reactions have been reported for PURIFIED WATER:

Other Drugs Associated with DEPRESSED MOOD

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

HYPERICUM PERFORATUM

Frequently Asked Questions

Does PURIFIED WATER cause DEPRESSED MOOD?

DEPRESSED MOOD has been reported as an adverse event in 2 FDA reports for PURIFIED WATER. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is DEPRESSED MOOD with PURIFIED WATER?

DEPRESSED MOOD accounts for approximately 1.5% of all adverse event reports for PURIFIED WATER, making it a notable side effect.

What should I do if I experience DEPRESSED MOOD while taking PURIFIED WATER?

If you experience depressed mood while taking PURIFIED WATER, 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

PURIFIED WATER Full ProfileAll Drugs Causing DEPRESSED MOODMcKesson 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.