LEVODOPA and TREMOR

Overview

TREMOR is the #11 most commonly reported adverse reaction for LEVODOPA, manufactured by Merz Pharmaceuticals, LLC. There are 507 FDA adverse event reports linking LEVODOPA to TREMOR. This represents approximately 1.9% of all 26,727 adverse event reports for this drug.

Patients taking LEVODOPA who experience tremor 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

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

Other Side Effects of LEVODOPA

In addition to tremor, the following adverse reactions have been reported for LEVODOPA:

• COUGH — 2,192 reports
• DRUG INEFFECTIVE — 1,358 reports
• PARKINSON^S DISEASE — 1,033 reports
• DYSKINESIA — 732 reports
• DEATH — 669 reports
• FALL — 667 reports
• CONDITION AGGRAVATED — 662 reports
• DEVICE ISSUE — 655 reports
• HALLUCINATION — 613 reports
• PRODUCT RESIDUE PRESENT — 541 reports

Other Drugs Associated with TREMOR

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

Does LEVODOPA cause TREMOR?

TREMOR has been reported as an adverse event in 507 FDA reports for LEVODOPA. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is TREMOR with LEVODOPA?

TREMOR accounts for approximately 1.9% of all adverse event reports for LEVODOPA, making it a notable side effect.

What should I do if I experience TREMOR while taking LEVODOPA?

If you experience tremor while taking LEVODOPA, 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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