Medication | Starting dose | Adverse effects | Comments | |
---|---|---|---|---|
Non-ergotamine dopamine agonists | Nausea, orthostasis, daytime somnolence; augmentation occurs, but less so than with carbidopa/levodopa(Sinemet) | Drugs of choice in most patients with moderate to severe daily RLS; pramipexole and ropinirole are FDA-indicated for the treatment of moderate to severe RLS Pramipexole: increase dose by 0.25 mg after four to seven days, up to 0.5 mg per day Ropinirole: increase to 0.5 mg on day three and to1.0 mg on day eight; increase by 0.5 mg every week if needed to maximum of 4 mg per day | ||
Pramipexole (Mirapex) | 0.125 mg | |||
Ropinirole (Requip) | 0.25 mg | |||
Carbidopa/levodopa | 25/100 mg | Gastrointestinal upset and headache; augmentation common with daily dosing | Rapid onset of action, usually with first dose; beneficial for individuals requiring medications for intermittent symptoms | |
Gabapentin (Neurontin) | 100 to 300 mg | Sedation, gastrointestinal discomfort | An appropriate first choice in individuals with RLS associated with neuropathic pain; consider use for daily RLS if dopamine agonist not effective; may be used with dopamine agonist in patients with refractory RLS | |
Opioids | Nightly dose varies by choice of opioid | Nausea, constipation; potential for abuse | Limited studies of effectiveness, but a reasonable choice in individuals with RLS associated with pain; may be used with dopamine agonist in patients with refractory RLS | |
Benzodiazepines | Daytime sleepiness; increased risk of falls at night; potential for abuse | Can be useful in intermittent RLS, particularly when insomnia is significant; may be used with dopamine agonist in patients with refractory RLS | ||
Clonazepam (Klonopin) | 0.5 mg | |||
Zolpidem (Ambien) | 5 mg | |||
Ergotamine dopamine agonists | Same as for non-ergotamine agonists; also have additional risk of cardiac valvulopathy | Effective in the treatment of moderate to severe RLS, but non-ergotamine dopamine agonists are preferred because of safety profile; neither cabergoline nor pergolide is FDA-indicated for treatment of RLS; pergolide recently removed from the U.S. market | ||
Cabergoline (Dostinex) | 0.5 mg | |||
Pergolide (Permax) | 0.05 mg |