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Dopamine Agonist — Transdermal Patch (Parkinson's / RLS)

Rotigotine

Brand names: Neupro

Rotigotine is a non-ergot dopamine agonist delivered via a transdermal patch, used in Parkinson's disease and in moderate-to-severe restless legs syndrome.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It stimulates dopamine receptors, principally D3, D2 and D1 subtypes, providing continuous dopaminergic stimulation through steady transdermal delivery.

Prescribing in practice

  • Dopamine agonists can cause impulse-control disorders and sudden-onset sleep, which patients and carers must be warned about and monitored for throughout treatment.
  • The patch backing of some formulations contains aluminium and should be removed before MRI or cardioversion to avoid burns.
  • Application-site reactions are common; the application site should be rotated and the patch not applied to the same area on consecutive days.

Monitoring

Monitor for impulse-control behaviours, excessive daytime somnolence, blood pressure (including postural drops) and local skin reactions.

Counselling the patient

  • Rotate the patch site each day and apply to clean, dry, intact skin to reduce skin reactions.
  • Report any new compulsive behaviours such as gambling or compulsive shopping to your clinician.
  • Be cautious with driving because of the risk of drowsiness and sudden sleep onset.

Evidence & guidelines

Rotigotine transdermal patches have demonstrated efficacy in randomised trials in both Parkinson's disease and restless legs syndrome and are recommended treatment options in NICE guidance.

Reference: NICE NG71 (Parkinson's Disease); MHRA ICD Warning; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.