Neupro

Neupro

Generic Name

Neupro

Brand Names

for *rotigotine*, a non‑ergot dopamine‑agonist administered via a transdermal patch. It is primarily indicated for the management of Parkinson’s disease (PD) and rest‑less legs syndrome (RLS).

Mechanism

  • Partial dopamine agonist
  • Selectively stimulates D₂, D₃, and D₄ dopamine receptors with high affinity, mimicking dopamine actions in basal ganglia circuits.
  • Sustained release
  • Continuous dermal delivery maintains steady plasma levels, avoiding the pulsatile dopaminergic stimulation associated with oral levodopa, thereby reducing motor fluctuations and dyskinesia.
  • Neuroprotective potential
  • Preclinical data suggest rotigotine may modulate α‑synuclein aggregation and reduce oxidative stress, although clinical benefit remains investigational.

Pharmacokinetics

ParameterKey Findings
AbsorptionDermal absorption yields a C_max of ~0.1 µg/mL by 6 h, with ~2.4 µg/mL at steady state (≈48 h).
Half‑life~3-5 h (but patch release extends effective half‑life).
Bioavailability18–23 % relative to oral dosing (patch bypasses first‑pass metabolism).
MetabolismHepatic via CYP2D6 and CYP3A4; metabolites inactive.
ExcretionPrimarily renal (≈60 %) and fecal.
Steady stateAchieved in ~5–7 days; patch replacement every 1–2 days (typically 3–5 µg/h → 5–7 µg/h patches).

Indications

  • Parkinson’s Disease
  • *Off‑time* therapy for motor fluctuations in patients receiving and/or unable to tolerate levodopa.
  • Adjunct to levodopa for early‑stage PD (controlled by the FDA).
  • Rest‑less Legs Syndrome (approved in some countries, off‑label in others).
  • Compulsive sexual behaviour (investigational; not FDA approved).

Contraindications

  • Contraindications
  • Known hypersensitivity to rotigotine or patch components.
  • Severe hepatic dysfunction (CR ≥3).
  • Warnings
  • Fluid retention / edema – monitor weight and signs of heart failure.
  • Psychiatric – risk of impulse control disorders, hallucinations, and mood changes.
  • Cardiogenic – potential bradycardia, hypotension, or syncope; avoid in severe cardiac disease or uncontrolled hypertension.
  • Precautions
  • Use with caution in patients with skin disorders (eczema, dermatitis) or scar tissue.
  • Avoid exposure to high temperatures (>38 °C) which can increase systemic levels.

Dosing

StagePatch StrengthDurationReplacement FrequencyDosing Notes
Initiation2 µg/h24 hEvery 3–5 days (per product labeling)Start at 2 µg/h; titrate upward by 2 µg/h increments weekly.
Maintenance4–7 µg/h24 hEvery 4–5 daysAdjust based on motor control & tolerability.

Patch Placement: Rotate sites (abdomen, flank, upper arm, thigh) to avoid skin irritation.
Patch Removal: If adverse cutaneous reaction occurs, remove patch and reapply at a different site with a temporary skin barrier.

Adverse Effects

Common (≥10 % incidence)
• Nausea, vomiting
• Somnolence, dizziness
• Dysphagia
• Abdominal pain, constipation

Serious (≤1 % incidence)
Impulse control disorders (punding, gambling, hypersexuality) – warrants patient education & monitoring.
Psychosis / hallucinations – assess baseline neuropsychiatric status.
Fluid retention with heart failure – monitor vitals, creatinine.
Hypotension – especially upon patch removal or high‑dose titration.

Monitoring

  • Clinical: Regular assessment of motor scores (UPDRS Part III), daytime sleepiness, and impulse control behaviors.
  • Vital signs: Blood pressure (supine and standing) and heart rate weekly during titration.
  • Signs of fluid overload: Weight, peripheral edema.
  • Skin changes: Inspect patch site daily for dermatitis or contact reactions.
  • Laboratory: Liver function tests quarterly; renal panel as clinically indicated.

Clinical Pearls

  • Avoid heat: The patch’s absorption increases at temperatures above 38 °C; instruct patients to limit sunbathing or hot tubs.
  • Patch‑Hematologic partner: For patients concurrently on anticoagulants, skin reactions can lead to local microvascular changes; monitor for petechiae or bruising.
  • “On‑off” transitions: Rapid removal of the patch can precipitate a sudden “off” state; if patients feel tremor resurgence within 75 yrs) tolerate lower basal doses (2 µg/h) and may benefit from slower titration due to altered pharmacokinetics.

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• *This drug card is for educational purposes and reflects the latest FDA‑approved indications and clinical data. Always consult current prescribing information and institutional guidelines when initiating therapy.*

Medical & AI Content Disclaimers
Medical Disclaimer: Medical definitions are provided for educational purposes and should not replace professional medical advice, diagnosis, or treatment.

AI Content Disclaimer: Some definitions may be AI-generated and may contain inaccuracies. Always verify with authoritative medical references.

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