Levodopa

If Parkinson's disease (PD) is suspected all patients regardless of age should be referred to a specialist untreated, for confirmation of the diagnosis and assessment.

Levodopa therapy should be initiated with low doses and gradually increased, by small increments. The final dose is usually a compromise between increased mobility and dose-limiting side effects.

Treatment should be initiated and modified by a healthcare professional with specialist expertise in Parkinson's disease (or following their advice).

Co-beneldopa

• Capsule 50mg/12.5mg, 100mg/25mg, 200mg/50mg (£11.78 = 200mg/50mg x 100 capsules)
• Dispersible tablet 50mg/12.5mg, 100mg/25mg (£10.45 = 100mg/25mg x 100 tablets)
• Madopar CR modified-release capsule 100mg/25mg (£12.77 = 100 capsules)

Indications

• Parkinson's disease

Dose (expressed as levodopa)

• Standard-release:
  • Adults: Initially 50mg 3–4 times daily (100mg 3 times daily in advanced disease), increased by 100mg daily once or twice weekly according to response; usual maintenance dose 400–800mg daily in divided doses
  • Elderly: initially 50mg once or twice daily, increased by 50mg daily every 3–4 days according to response
• Modified-release:
  • Patients not taking levodopa/dopa-decarboxylase inhibitor therapy: initially 1 capsule 3 times daily (maximum initial dose 6 capsules daily)
  • Patients transferring from immediate-release levodopa/dopa-decarboxylase inhibitor preparations: Initially 1 capsule substituted for every 100mg of levodopa and given at same dosage frequency, increased every 2–3 days according to response; average increase of 50% needed over previous levodopa dose and titration may take up to 4 weeks
  • Supplementary dose of immediate-release may be needed with first morning dose: If response still poor to total daily dose corresponding to 1.2 g levodopa, consider alternative therapy

Notes

1. Madopar CR modified-release capsules contain soya oil and are contraindicated in patients allergic to peanut or soya.

Co-careldopa

• Tablet 50mg/12.5mg, 100mg/10mg, 100mg/25mg, 250mg/25mg (£35.00 = 250mg/25mg x 100 tablets)
• Half Sinemet CR modified-release tablet 100mg/25mg (£11.60 = 60 tablets)
• Sinemet CR modified-release tablet 200mg/50mg (£11.60 = 60 tablets)

Indications

• Parkinson's disease

Dose (expressed as levodopa)

• Standard-release:
  • Adults: Initially 100mg (with carbidopa 25mg) 3 times daily, increased by 50–100mg (with carbidopa 12.5 or 25mg) daily or on alternate days according to response, up to 800mg (with carbidopa 200mg) daily in divided doses
  • Alternative regime: Initially levodopa 50–100mg (with carbidopa 10 or 12.5mg) 3–4 times daily, increased by 50–100mg daily or on alternate days according to response, up to 800mg (with carbidopa 80 or 100mg) daily in divided doses
• Modified-release:
  • Patients not receiving levodopa/dopa-decarboxylase inhibitor therapy: Initially, 1 Sinemet CR tablet twice daily; both dose and interval then adjusted according to response at intervals of not less than 3 days
  • Patients transferring from immediate-release levodopa/dopa-decarboxylase inhibitor preparations: 1 Sinemet CR tablet twice daily can be substituted for a daily dose of levodopa 300–400mg in immediate-release Sinemet tablets (substitute Sinemet CR to provide approx. 10% more levodopa per day and extend dosing interval by 30–50%); dose and interval then adjusted according to response at intervals of not less than 3 days

Notes

1. When co-careldopa is used, the total daily dose of carbidopa should be at least 70mg. A lower dose may not achieve full inhibition of extra cerebral dopa-decarboxylase with a resultant increase in side effects.

With entacapone

Sastravi

(Combination of levodopa / carbidopa / entacapone)

• Tablets (50mg/ 12.5mg/ 200mg), (75mg/ 18.75mg/ 200mg), (100mg/ 25mg/ 200mg), (125mg/ 31.25mg/ 200mg), (150mg/ 37.5mg/ 200mg), (175mg/ 43.75mg/ 200mg), (200mg/ 50mg/ 200mg) (£34.66 = 100 tablets (all strengths))

Indications

• For Parkinson's disease and end-of-dose motor fluctuations not adequately controlled with levodopa and dopa-decarboxylase inhibitor treatment

Dose

• Only 1 tablet to be taken for each dose; maximum 10 tablets daily (50-150mg levodopa), maximum 8 tablets daily (175mg levodopa), maximum 7 tablets daily (200mg levodopa)

Notes

1. Prescribe by brand (to aid identification where products contain multiple ingredients, or to prevent confusion where multiple brands contain similar ingredients).

Catechol-O-methyltransferase inhibitors (COMTI)

Treatment should be initiated and modified by a healthcare professional with specialist expertise in Parkinson's disease (or following their advice).

Entacapone

• Tablets 200mg (£7.85 = 30 tablets)

Indications

• Adjunct to co-beneldopa or co-careldopa in Parkinson's disease with 'end of dose' motor fluctuations (under expert supervision)

Dose

• 200mg with each dose of levodopa with dopa-decarboxylase inhibitor; maximum 10 tablets (2g) per day

Notes:

1. It is important than Entacapone and co-beneldopa or co-careldopa are taken together at the same time of day.
2. It may be necessary to reduce the concurrent levodopa dose by 10-30%.

Opicapone

• Tablets 50mg (£59.00 = 30 tablets)

Indications

• Adjunct to co-beneldopa or co-careldopa in Parkinson's disease with 'end of dose' motor fluctuations (under expert supervision)

Dose

• 50mg once daily at bedtime, at least one hour before or after levodopa combinations; review after 3 months

Notes

1. To be used only where entacapone is not tolerated or unsuccessful.
2. Treatment should be initiated and reviewed by specialists. Following a successful 3 month trial, ongoing prescribing may be undertaken in primary care.
3. It may be necessary to reduce the concurrent levodopa dose.
4. The routine commissioning of opicapone is accepted in Devon for the treatment of patients with Parkinson's disease who have not been able to tolerate entacapone (see Commissioning Policy for more details).

Tolcapone

• Tablets 100mg

Indications

• Adjunct to co-beneldopa or co-careldopa in Parkinson's disease with 'end-of-dose' motor fluctuations if another inhibitor of peripheral COMT inappropriate (under specialist supervision)

Notes

1. To be prescribed by a Parkinson's disease specialist only.
2. Tolcapone requires specialist monitoring. It should only be used if entacapone fails.
3. Hepatotoxicity: potentially life-threatening hepatotoxicity including fulminant hepatitis reported rarely, usually in women and during the first 6 months, but late-onset liver injury also reported; test liver function before treatment, and monitor every 2 weeks for first year, every 4 weeks for next 6 months and then every 8 weeks thereafter (restart monitoring schedule if dose increased). Discontinue if abnormal liver function tests or symptoms of liver disorder, do not re-introduce tolcapone once discontinued.
4. Patients should be told how to recognise signs of liver disorder and advised to seek immediate medical attention if symptoms such as anorexia, nausea, vomiting, fatigue, abdominal pain, dark urine, or pruritus develop.

Dopamine receptor agonists

Local specialists have indicated that ergot derived dopamine receptor agonists are not routinely used in the treatment of Parkinson's disease. More information on these treatment options can be found in 6.7.1 Bromocriptine and other dopaminergic drugs.

Treatment should be initiated and modified by a healthcare professional with specialist expertise in Parkinson's disease (or following their advice).

Patients and their carers should be informed about the risk of impulse control disorders (including pathological gambling, binge eating, and hypersexuality) associated with dopamine-receptor agonists. There is no evidence that ergot- and non-ergot-derived dopamine-receptor agonists differ in their propensity to cause impulse control disorders, so switching between dopamine-receptor agonists to control these side-effects is not recommended. If the patient develops an impulse control disorder, the dopamine-receptor agonist should be withdrawn or the dose reduced until the symptoms resolve.

Apomorphine

• APO-go solution for injection ampoules 50mg/5ml
• APO-go PEN solution for injection pre-filled disposable devices 30mg/3ml
• APO-go PFS solution for infusion pre-filled syringes 50mg/10ml
• APO-go POD solution for infusion cartridges 100mg/20ml

Indications

• Refractory motor fluctuations in Parkinson's disease ('off' episodes) inadequately controlled by co-beneldopa or co-careldopa or other dopaminergics (for capable and motivated patients, under specialist supervision)

Notes

1. Prescribe by brand to prevent confusion. Patient familiarity with one brand is important; instructions for use vary between preparations and user training is required.
2. Apomorphine is sometimes helpful in stabilising patients experiencing unpredictable "off" periods with levodopa treatment. It is essential to stabilise patients on domperidone for at least 2 days before starting treatment with apomorphine.
3. MHRA Drug Safety Alert (April 2016): Patients receiving apomorphine and domperidone require an assessment of cardiac risk factors and ECG monitoring to reduce the risk of serious arrhythmia related to QT-prolongation
   1. Before starting treatment, carefully consider whether the benefits of concomitant apomorphine and domperidone treatment outweigh the small increased risk of cardiac side effects.
   2. Discuss the benefits and risks of apomorphine with patients and carers and advise them to contact their doctor immediately if they develop palpitations or syncopal symptoms during treatment.
   3. Check the QT-interval before starting domperidone, during the apomorphine initiation phase and if clinically indicated thereafter (eg if a QT-prolonging or interacting drug is started or if symptoms of cardiac side effects are reported).
   4. Regularly review domperidone treatment to ensure patients take the lowest effective dose for the shortest duration. See section 4.6 Drugs used in nausea and vertigo.
   5. Advise patients to inform their doctor of any changes that could increase their risk of arrhythmia, such as:
      1. symptoms of cardiac or hepatic disorders
      2. conditions that could cause electrolyte disturbances (eg, gastroenteritis or starting a diuretic)
      3. starting any other medicines.

Amantadine

• Capsules 100mg (£6.21 = 56 capsules)
• Oral solution sugar free 50mg/5ml (£140.00 = 150ml)

Indications

• Parkinson's disease

Dose

• Adults: 100mg daily increased after one week to 100mg twice daily, usually in conjunction with other treatment; some patients may require higher doses, maximum 400mg daily.
• Elderly: 100mg daily adjusted according to response

Notes

1. Amantadine has modest antiparkinsonian effects. It improves mild bradykinetic disabilities as well as tremor and rigidity. Unfortunately, only a small proportion of patients derive much benefit from this drug and tolerance to its effects occurs.
2. May be useful for the control of dyskinesia.

Pramipexole

• Tablets 88micrograms, 180micrograms, 350micrograms, 700micrograms (£43.57 = 350micrograms three times a day)
• Modified-release tablets 260micrograms, 520micrograms, 1.05mg, 1.57mg, 2.1mg, 2.62mg, 3.15mg (click here for preferred brand)

Indications

• Parkinson's disease, used alone or as an adjunct to co-beneldopa or co-careldopa

Dose

• Standard-release: Initially 88micrograms (base) 3 times daily, dose doubled every 5–7 days if tolerated to 350micrograms 3 times daily; further increased if necessary by 180micrograms 3 times daily at weekly intervals; maximum 3.3mg daily in 3 divided doses
• Modified-release: Initially 260micrograms (base) once daily, dose doubled every 5–7 days to 1.05mg once daily; further increased if necessary by 520micrograms daily at weekly intervals; maximum 3.15mg once daily

Notes

1. Exercise caution when prescribing, dispensing and administering pramipexole as the packs may express dose as both the base and the dihydrochloride salt. For equivalence / conversion between base and salt, refer to BNF. Doses above are expressed in terms of pramipexole base.
2. Where a preferred brand is recommended for a particular presentation, prescribing by brand helps ensure cost-efficient use of local NHS resources (see preferred brand link above).

Ropinirole

• Tablet 0.25mg, 0.5mg, 1mg, 2mg, 5mg (£195.92 = 15mg daily)
• Modified-release tablets 2mg, 3mg, 4mg, 6mg, 8mg click here for preferred brand)

Indications

• Parkinson's disease, either used alone or as adjunct to co-beneldopa or co-careldopa

Dose

• Standard-release: Initially 750micrograms daily in 3 divided doses, increased by increments of 750micrograms daily at weekly intervals to 3mg daily in 3 divided doses; further increased by increments of 1.5–3mg daily at weekly intervals according to response; usual range 9–16mg daily in 3 divided doses (but higher doses may be required if used with levodopa); maximum 24mg daily in 3 divided doses
• Modified-release: Initially 2mg once daily for 1 week, then 4mg once daily; increased according to response by 2mg at intervals of at least 1 week up to 8mg once daily; if still no response, increase by 2–4mg at intervals of at least 2 weeks as necessary; maximum 24mg once daily

Notes

1. Where a preferred brand is recommended for a particular presentation, prescribing by brand helps ensure cost-efficient use of local NHS resources (see preferred brand link above).

Rotigotine

• Patches 2mg/24hours, 4mg/24hours, 6mg/24hours, 8mg/24hours (£149.93 = 6mg/24hours daily)

Indications

• Parkinson's disease, either used alone or as adjunct to co-beneldopa or co-careldopa

Dose

• Monotherapy in early-stage Parkinson's disease: Initially apply '2mg/24hours' patch, increased in steps of 2 mg/24hours at weekly intervals if required; maximum 8mg/24hours.
• Adjunctive therapy with levodopa with advanced stage Parkinson's disease with motor fluctuations: Initially apply '4mg/24hours' patch, increased in steps of 2mg/24hours at weekly intervals if required; maximum 16mg/24hours

Notes

1. Transdermal rotigotine should only be prescribed for patients unable to take oral medication or for patients with motor complications who have failed therapy with other dopamine agonists.
2. Patches should be applied to dry, non-irritated skin on torso, thigh or upper arm. Patches should be removed after 24 hours and the replacement patch applied on a different area (avoid using the same area for 14 days).

Monoamine-oxidase-B inhibitors

Treatment should be initiated and modified by a healthcare professional with specialist expertise in Parkinson's disease (or following their advice).

Rasagiline

• Tablets 1mg (£24.25)

Indications

• Parkinson's disease, used alone or as adjunct to co-beneldopa or co-careldopa for 'end-of-dose' fluctuations

Dose

• 1mg daily

Selegiline

• Tablet 5mg, 10mg (£9.02 = 10mg daily)

Indications

• Parkinson's disease, used alone or as adjunct to co-beneldopa or co-careldopa to reduce 'end of dose' deterioration; symptomatic parkinsonism

Dose

• Initially 5mg in the morning; increasing after 2–4 weeks if tolerated to 10mg in the morning

Safinamide (Xadago)

The routine commissioning of Safinamide (Xadago) is not accepted in Devon for patients with mid-to-late stage fluctuating Parkinson's disease. (see Commissioning Policy for more details).

Dopa derivatives

Foslevodopa-foscarbidopa

• Solution for infusion vial 2.4g/10ml / 120mg/10ml

Notes

1. NICE TA934: Foslevodopa-foscarbidopa (Produodopa) is recommended as an option for treating advanced levodopa-responsive Parkinson’s in adults whose symptoms include severe motor fluctuations and hyperkinesia or dyskinesia, when available medicines are not working well enough (November 2023), only if:
   1. they cannot have apomorphine or deep brain stimulation, or these treatments no longer control symptoms, and
   2. the company provides foslevodopa-foscarbidopa according to the commercial arrangement.
2. Foslevodopa and foscarbidopa are prodrugs equivalent to approximately 170mg levodopa and 9mg carbidopa per 1ml.