ROTIGOTINE and NAUSEA

Overview

NAUSEA is the #10 most commonly reported adverse reaction for ROTIGOTINE, manufactured by UCB, Inc.. There are 517 FDA adverse event reports linking ROTIGOTINE to NAUSEA. This represents approximately 1.8% of all 28,260 adverse event reports for this drug.

Patients taking ROTIGOTINE 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 a less commonly reported adverse event for ROTIGOTINE, but still significant enough to appear in the safety profile.

Other Side Effects of ROTIGOTINE

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

• PRODUCT ADHESION ISSUE — 1,793 reports
• DRUG INEFFECTIVE — 1,097 reports
• FALL — 941 reports
• DEATH — 907 reports
• OFF LABEL USE — 809 reports
• PARKINSON^S DISEASE — 759 reports
• HALLUCINATION — 684 reports
• DYSKINESIA — 622 reports
• TREMOR — 604 reports
• DIZZINESS — 480 reports

Other Drugs Associated with NAUSEA

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

Does ROTIGOTINE cause NAUSEA?

NAUSEA has been reported as an adverse event in 517 FDA reports for ROTIGOTINE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is NAUSEA with ROTIGOTINE?

NAUSEA accounts for approximately 1.8% of all adverse event reports for ROTIGOTINE, making it a notable side effect.

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

If you experience nausea while taking ROTIGOTINE, 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.

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