Neupro

— THERAPEUTIC CATEGORIES —
  • Parkinsonism
  • Restless legs syndrome

Neupro Generic Name & Formulations

General Description

Rotigotine 1mg/24hrs, 2mg/24hrs, 3mg/24hrs, 4mg/24hrs, 6mg/24hrs, 8mg/24hrs; transdermal patch; contains sodium metabisulfite.

Pharmacological Class

Dopamine agonist (non-ergot).

How Supplied

Patches—30

Manufacturer

Generic Availability

NO

Neupro Indications

Indications

Idiopathic Parkinson's disease.

Neupro Dosage and Administration

Adult

Apply to clean, dry, intact skin on abdomen, thigh, hip, flank, shoulder, or upper arm. Early-stage: initially 2mg/24hrs patch once daily; may increase weekly by 2mg/24hrs if needed; max 6mg/24hrs once daily. Advanced-stage: initially 4mg/24hrs patch once daily; may increase weekly by 2mg/24hrs if needed; max 8mg/24hrs once daily. Rotate application site (allow 14 days before reapplying to same site). Shave site at least 3 days before application if hairy. Avoid abrupt cessation; reduce by 2mg/24hrs every other day.

Children

Not established.

Neupro Contraindications

Not Applicable

Neupro Boxed Warnings

Not Applicable

Neupro Warnings/Precautions

Warnings/Precautions

Avoid external heat sources. Remove patch before cardioversion, MRI. Consider discontinuing if excessive daytime sleepiness or falling asleep during activities occurs. Sleep disorder. Psychotic disorder. Increased risk of symptomatic hypotension; monitor BP esp. during dose adjustments. Cardiovascular disease. Conditions aggravated by fluid retention (eg, CHF, renal insufficiency); monitor for weight gain. Consider dose reduction or discontinuation if urges/compulsive behaviors develop. Asthma. Sulfite sensitivity. Pre-existing dyskinesia. Potential withdrawal symptoms; monitor during and after discontinuation. Severe hepatic impairment. Pregnancy. Nursing mothers: may inhibit lactation.

Neupro Pharmacokinetics

See Literature

Neupro Interactions

Interactions

Caution with concomitant alcohol, sedating drugs or other CNS depressants (eg, benzodiazepines, antipsychotics, antidepressants). May be antagonized by metoclopramide, antipsychotics.

Neupro Adverse Reactions

Adverse Reactions

Nausea, vomiting, somnolence (may be sudden), application site reactions, dizziness, anorexia, hyperhidrosis, insomnia, peripheral edema, dyskinesia; orthostatic hypotension, syncope, hallucinations, psychotic-like behavior, intense urges/compulsions, hypertension, heart rate elevation.

Neupro Clinical Trials

See Literature

Neupro Note

Not Applicable

Neupro Patient Counseling

See Literature

Neupro Generic Name & Formulations

General Description

Rotigotine 1mg/24hrs, 2mg/24hrs, 3mg/24hrs, 4mg/24hrs, 6mg/24hrs, 8mg/24hrs; transdermal patch; contains sodium metabisulfite.

Pharmacological Class

Dopamine agonist (non-ergot).

How Supplied

Patches—30

Manufacturer

Generic Availability

NO

Neupro Indications

Indications

Moderate to severe primary restless legs syndrome (RLS).

Neupro Dosage and Administration

Adult

Apply to clean, dry, intact skin on abdomen, thigh, hip, flank, shoulder, or upper arm. Initially 1mg/24hrs patch once daily; may increase weekly by 1mg/24hrs if needed; max 3mg/24hrs once daily. Rotate application site (allow 14 days before reapplying to same site). Shave site at least 3 days before application if hairy. Avoid abrupt cessation; reduce by 1mg/24hrs every other day.

Children

Not established.

Neupro Contraindications

Not Applicable

Neupro Boxed Warnings

Not Applicable

Neupro Warnings/Precautions

Warnings/Precautions

Avoid external heat sources. Remove patch before cardioversion, MRI. Consider discontinuing if excessive daytime sleepiness or falling asleep during activities occurs. Sleep disorder. Psychotic disorder. Increased risk of symptomatic hypotension; monitor BP esp. during dose adjustments. Cardiovascular disease. Conditions aggravated by fluid retention (eg, CHF, renal insufficiency); monitor for weight gain. Consider dose reduction or discontinuation if urges/compulsive behaviors develop. Asthma. Sulfite sensitivity. Pre-existing dyskinesia. Potential withdrawal symptoms; monitor during and after discontinuation. Severe hepatic impairment. Pregnancy. Nursing mothers: may inhibit lactation.

Neupro Pharmacokinetics

See Literature

Neupro Interactions

Interactions

Caution with concomitant alcohol, sedating drugs or other CNS depressants (eg, benzodiazepines, antipsychotics, antidepressants). May be antagonized by metoclopramide, antipsychotics.

Neupro Adverse Reactions

Adverse Reactions

Nausea, vomiting, somnolence (may be sudden), application site reactions, headache, dizziness, anorexia, hyperhidrosis, insomnia, peripheral edema, dyskinesia; orthostatic hypotension, syncope, hallucinations, psychotic-like behavior, intense urges/compulsions, hypertension, heart rate elevation, augmentation/rebound of RLS symptoms.

Neupro Clinical Trials

See Literature

Neupro Note

Not Applicable

Neupro Patient Counseling

See Literature