GNH USA

Europe — EMA

Neupro (Rotigotine)

GNH USA supplies Neupro (Rotigotine), a dopamine agonist for Parkinson's disease and restless legs syndrome. Request a quote for worldwide supply.

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What is Rotigotine?

Rotigotine, the active ingredient in Neupro, is a dopamine agonist presented as a 2‑8 mg/24 h transdermal patch for transdermal use. It treats Parkinson's disease and restless legs syndrome in adults.

GNH USA supplies Neupro as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Rotigotine used for?

Neupro is a dopamine agonist indicated for movement‑disorder conditions.

- Parkinson's disease: improves motor symptoms and reduces OFF periods in patients with idiopathic Parkinson's disease. - Restless legs syndrome: lessens the urge to move the legs and improves sleep quality in adults with moderate to severe RLS.

What are the side effects of Rotigotine?

Common Side Effects: - Application site reactions: erythema, pruritus, or edema at the patch site. - Nausea or vomiting. - Dizziness or light‑headedness. - Somnolence or fatigue. - Dry mouth. - Increased sweating.

Serious or Rare Side Effects: - Hallucinations or psychotic symptoms. - Impulse control disorders such as compulsive gambling or hypersexuality. - Severe hypotension or syncope. - Allergic reactions including skin necrosis or anaphylaxis.

What precautions apply to Rotigotine?

Before initiating therapy, clinicians should evaluate patient‑specific risk factors. - Cardiovascular assessment: monitor for orthostatic hypotension, especially in elderly patients. - Psychiatric history: watch for hallucinations, confusion, or impulse control disorders. - Hepatic function: consider dose adjustment in moderate hepatic impairment. - Concomitant dopamine antagonists: avoid or use with caution due to antagonistic effects. - Hypersensitivity: discontinue if allergic reaction to rotigotine or patch excipients occurs. - Store at room temperature: keep in the original pouch, protect from moisture and direct sunlight.

What does Rotigotine interact with?

Rotigotine may interact with several drug classes.

Major Interactions (Avoid): - MAO‑B inhibitors (e.g., selegiline, rasagiline): risk of hypertensive crisis. - Strong CYP1A2 inhibitors (e.g., fluvoxamine): may increase rotigotine exposure. - Potent CYP2C19 inhibitors (e.g., omeprazole): can raise plasma levels. - Antipsychotics with dopamine antagonism (e.g., haloperidol): reduce therapeutic effect. - Other dopamine agonists: additive dopaminergic effects.

Moderate Interactions (Monitor Closely): - Antihypertensives: enhanced hypotensive effect. - CYP3A4 inducers (e.g., carbamazepine, rifampicin): may lower rotigotine concentrations. - Alcohol: may increase central nervous system depression. - SSRIs or SNRIs: potential for increased nausea. - Nicotine replacement therapy: may affect patch adhesion and absorption.

Frequently asked questions

What conditions is Neupro used to treat?+
Neupro is prescribed for adults with Parkinson's disease to improve motor function and reduce OFF periods, and for patients with moderate to severe restless legs syndrome to lessen leg discomfort and improve sleep quality.
How does rotigotine work in the body?+
Rotigotine is delivered continuously through a skin patch, where it is absorbed into the bloodstream. It activates dopamine D1, D2, and D3 receptors in the brain, restoring dopaminergic signaling that is deficient in Parkinson's disease and restless legs syndrome.
What is the usual dose of Neupro?+
The prescribed dose of Neupro is individualized. A healthcare professional selects the appropriate patch strength (2 mg/24 h, 4 mg/24 h, 6 mg/24 h, or 8 mg/24 h) and determines the dosing schedule based on the patient’s clinical response and tolerability.
Is Neupro safe to use during pregnancy or breastfeeding?+
The safety of rotigotine in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by the prescribing clinician.
How do I order Neupro from GNH USA?+
To place an order, submit an enquiry on the Neupro product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.
How does Neupro compare with other dopamine agonists?+
Neupro provides continuous dopaminergic stimulation via a transdermal system, which can reduce motor fluctuations compared with oral dopamine agonists that have peak‑and‑trough plasma levels. However, it may have a higher incidence of skin‑related reactions at the application site.
What are the recommended storage conditions for Neupro?+
Neupro patches should be stored at room temperature, below 25 °C, in the original packaging. Keep them away from moisture, direct sunlight, and heat sources to maintain patch integrity and drug stability.
How is Neupro applied and administered?+
A single patch is applied to clean, dry, hair‑free skin on the upper torso, upper arm, or thigh. The patch is worn for 24 hours and then replaced with a new one at the same time each day. Rotate application sites to minimize skin irritation.
What are the most serious risks associated with Neupro?+
Serious risks include hallucinations, impulse control disorders (such as compulsive gambling or hypersexuality), severe hypotension, and rare allergic reactions that may lead to skin necrosis or anaphylaxis. Patients should be monitored closely for these events.
Who should not use Neupro?+
Neupro is contraindicated in patients with known hypersensitivity to rotigotine or any component of the patch, and it should be avoided in individuals with severe hepatic impairment or those taking MAO‑B inhibitors. Clinicians must assess each patient’s medical history before prescribing.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Rotigotine
Route
Transdermal Use
Manufacturer
Ucb Pharma S.A.
Origin
EU

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