PRUCALOPRIDE and FATIGUE

Overview

FATIGUE is the #8 most commonly reported adverse reaction for PRUCALOPRIDE, manufactured by Takeda Pharmaceuticals America, Inc.. There are 126 FDA adverse event reports linking PRUCALOPRIDE to FATIGUE. This represents approximately 2.6% of all 4,835 adverse event reports for this drug.

Patients taking PRUCALOPRIDE who experience fatigue 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

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

Other Side Effects of PRUCALOPRIDE

In addition to fatigue, the following adverse reactions have been reported for PRUCALOPRIDE:

• DRUG INEFFECTIVE — 252 reports
• HEADACHE — 230 reports
• NAUSEA — 185 reports
• NO ADVERSE EVENT — 171 reports
• DIARRHOEA — 156 reports
• OFF LABEL USE — 154 reports
• CONSTIPATION — 126 reports
• INABILITY TO AFFORD MEDICATION — 120 reports
• DIZZINESS — 117 reports
• PRODUCT USE ISSUE — 106 reports

Other Drugs Associated with FATIGUE

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

Does PRUCALOPRIDE cause FATIGUE?

FATIGUE has been reported as an adverse event in 126 FDA reports for PRUCALOPRIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is FATIGUE with PRUCALOPRIDE?

FATIGUE accounts for approximately 2.6% of all adverse event reports for PRUCALOPRIDE, making it a notable side effect.

What should I do if I experience FATIGUE while taking PRUCALOPRIDE?

If you experience fatigue while taking PRUCALOPRIDE, 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