PRUCALOPRIDE and NAUSEA

Overview

NAUSEA is the #3 most commonly reported adverse reaction for PRUCALOPRIDE, manufactured by Takeda Pharmaceuticals America, Inc.. There are 185 FDA adverse event reports linking PRUCALOPRIDE to NAUSEA. This represents approximately 3.8% of all 4,835 adverse event reports for this drug.

Patients taking PRUCALOPRIDE who experience nausea 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

NAUSEA is moderately reported among PRUCALOPRIDE users, representing a notable but not dominant share of adverse events.

Other Side Effects of PRUCALOPRIDE

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

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

Other Drugs Associated with NAUSEA

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

Does PRUCALOPRIDE cause NAUSEA?

NAUSEA has been reported as an adverse event in 185 FDA reports for PRUCALOPRIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is NAUSEA with PRUCALOPRIDE?

NAUSEA accounts for approximately 3.8% of all adverse event reports for PRUCALOPRIDE, making it one of the most commonly reported side effect.

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

If you experience nausea 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