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ROPINIROLE SR is a brand name for Ropinirole. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Ropinirole SR is indicated in adults for Treatment of Parkinson's disease under the following conditions: • Initial treatment as monotherapy, in order to delay the introduction of levodopa • In combination with levodopa, over the course of the disease, when the effect of levodopa wears off or becomes inconsistent and…
Verbatim from this product's MHRA label. Tap a section to expand.
Posology Adults Individual dose titration against efficacy and tolerability is recommended. Initial titration The starting dose is 2 mg ropinirole once daily for the first week; this should be increased to 4 mg ropinirole once daily from the second week of treatment.
A therapeutic response may be seen at a dose of 4 mg once daily of prolonged-release tablets. The prolonged-release tablets should be taken once a day and at a similar time each day. The tablets may be taken with or without food. 2). Patients who initiate treatment with a dose of 2 mg/day of ropinirole prolonged- release tablets and who experience undesirable effects that they cannot tolerate, may benefit from switching to treatment with ropinirole immediate release tablets at a lower daily dose, divided into three equal doses.
Therapeutic regimen Patients should be maintained on the lowest dose of ropinirole prolonged-release tablets that achieves symptomatic control. If sufficient symptomatic control is not achieved or maintained at a dose of 4 mg once daily of ropinirole prolonged release tablets, the daily dose may be increased by 2 mg at weekly or longer intervals up to a dose of 8 mg once daily of prolonged-release tablets.
If sufficient symptomatic control is still not achieved or maintained at a dose of 8 mg once daily of ropinirole prolonged-release tablets, the daily dose may be increased by 2 mg to 4 mg at two weekly or longer intervals. The maximum daily dose of ropinirole prolonged-release tablets is 24 mg.
It is recommended that patients are prescribed the minimum number of ropinirole prolonged-release tablets that are necessary to achieve the required dose by utilising the highest available strengths of ropinirole prolonged-release tablets.
If treatment is interrupted for one day or more,re-initiation by dose titration should be considered (see above) When ropinirole prolonged-release tablets are administered as adjunct therapy to levodopa, it may be possible to gradually reduce the levodopa dose, depending on the clinical response.
In clinical trials, the levodopa dose was reduced gradually by approximately 30% in patients receiving ropinirole prolonged-release tablets concurrently. In patients with advanced Parkinson's disease receiving ropinirole prolonged-release tablets in combination with L-dopa, dyskinesias can occur during the initial titration of ropinirole prolonged-release tablets.
Adverse events are listed below by system organ class and frequency. It is noted if these undesirable effects were reported in clinical trials as monotherapy or adjunct therapy to levodopa. Frequencies are defined as: very common (≥ 1/10), common (≥ 1/100 to <1/10), uncommon (≥ 1/1,000 to <1/100), rare (≥ 1/10,000 to <1/1,000) very rare (<1/10,000), not known (cannot be estimated from the available data).
Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness. The following adverse drug reactions have been reported in either Parkinson’s disease clinical trials with <Ropinirole SR prolonged-release or film-coated (immediate- release) tablets at doses up to 24 mg/day, or from post-marketing reports: In monotherapy In adjunct therapy Immune system disorders Not known Hypersensitivity reactions (including urticaria, angioedema, rash, pruritus).
Psychiatric disorders Common Hallucinations Confusion Uncommon Psychotic reactions (other than hallucinations) including delirium, delusion, paranoia. 4). Aggression* Dopamine dysregulation syndrome Nervous system disorders Somnolence Somnolence**Very common Syncope Dyskinesia*** Common Dizziness (including vertigo), sudden onset of sleep Uncommon Excessive day time somnolence Vascular disorders Common Postural hypotension, hypotension Uncommon Postural hypotension, hypotension Gastrointestinal disorders Very common Nausea Nausea **** Common Constipation, heartburn Vomiting, abdominal pain Hepatobiliary disorders Not known Hepatic reactions, mainly increased liver enzymes General disorders and administration site conditions Oedema peripheralCommon Leg oedema Not known Dopamine agonist withdrawal syndrome (including apathy, anxiety, depression, fatigue, sweating and pain)***** Reproductive system and breast disorders Not know Spontaneous penile erection Respiratory, thoracic and mediastinal disorders Uncommon Hiccups *Aggression has been associated with psychotic reactions as well as compulsivesymptoms.
Ropinirole has been associated with somnolence and episodes of sudden sleep onset, particularly in patients with Parkinson's disease. 8). Patients must be informed of this and advised to exercise caution while driving or operating machines during treatment with ropinirole.
Patients who have experienced somnolence and/or an episode of sudden sleep onset must refrain from driving or operating machines. Reduction of dose or termination of therapy may be considered. Patients with a major psychotic disorders or a history of these disorders, should only be treated with dopamine agonists if the potential benefits outweigh the risks.
Impulse control disorders Patients should be regularly monitored for the development of impulse control disorders. Patients and carers should be made aware that behavioral symptoms of impulse control disorders including pathological gambling, increased libido, hypersexuality, compulsive spending or buying, binge eating, and compulsive eating can occur in patients treated with dopamine agonists including ropinirole.
Dose reduction/tapered discontinuation should be considered if such symptoms develop. Neuroleptic malignant syndrome Symptoms suggestive of neuroleptic malignant syndrome have been reported with abrupt withdrawal of dopaminergic therapy.
2). Ropinirole SR prolonged released tablets are designed to release ropinirole over a 24hr period. If rapid gastrointestinal transit occurs, there may be risk of incomplete release of the active substance, and of residue of the medicinal product being passed in the stool.
Due to the risk of hypotension, blood pressure monitoring is recommended, particularly at the start of treatment, in patients with severe cardiovascular disease (in particular coronary insufficiency). 2). Nonmotor adverse effects may occur when tapering or discontinuing dopamine agonists including ropinirole.
1. • Severe renal impairment (creatinine clearance <30 ml/min) without regular haemodialysis. • Hepatic impairment.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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8). When switching treatment from another dopamine agonist to ropinirole, the marketing authorisation holder's guidance on discontinuation should be followed before initiating ropinirole. 4). Switching from ropinirole immediate release tablets to ropinirole prolonged-release tablets Patients may be switched overnight from ropinirole immediate release tablets to ropinirole prolonged-release tablets.
5 - 9 8 12 12 15 - 18 16 21 20 24 24 After switching to ropinirole prolonged-release tablets, the dose may be adjusted depending on the therapeutic response (see “Initial titration” and “Therapeutic regimen” above). Special populations Elderly The clearance of ropinirole is decreased by approximately 15% in patients aged 65 years or above.
Although a dose adjustment is not required, ropinirole dose should be individually titrated, with careful monitoring of tolerability, to the optimal clinical response. In patients aged 75 years and above, slower titration during treatment initiation may be considered.
Renal impairment In patients with mild to moderate renal impairment (creatinine clearance between 30 and 50 ml/min) no change in the clearance of ropinirole was observed, indicating that no dose adjustment is necessary in this population.
A study into the use of ropinirole in patients with end stage renal disease (patients on haemodialysis) has shown that a dose adjustment in these patients is required as follows: The recommended initial dose of ropinirole is 2 mg once daily.
Further dose escalations should be based on tolerability and efficacy. The recommended maximum dose is 18 mg/day in patients receiving regular haemodialysis. 2). The use of ropinirole in patients with severe renal impairment (creatinine clearance less than 30 ml/min) without regular haemodialysis has not been studied.
Ropinirole SR is not recommended for use in this age group. Method of administration For oral use. The tablets must be swallowed whole and must not be chewed, crushed or divided.
** Somnolence has been reported very commonly in the adjunct therapy immediate - release clinical trials, and commonly in the adjunct therapy prolonged- release clinical trials. *** In patients with advanced Parkinson’s disease, dyskinesias can occur during the initial titration of ropinirole.
2). ****Nausea has been reported very commonly in the adjunct therapy immediate - release clinical trials, and commonly in the adjunct therapy prolonged- release clinical trials. 4). Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important.
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Symptoms include apathy, anxiety, depression, fatigue, sweating and pain which may be severe. Patients should be informed about this before tapering the dopamine agonist, and monitored regularly thereafter. 8). Hallucinations Hallucinations are known as an undesirable effect of treatment with dopamine agonists and levodopa.
Patients should be informed that hallucinations can occur. Ropinirole SR 2 mg and 3 mg prolonged release tablets The prolonged-release tablets contain lactose. Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicinal product.
Ropinirole SR 3 mg and 4 mg prolonged release tablets The prolonged-release tablets contain the azo colouring agent sunset yellow (E110), which may cause allergic reactions.