Tolerability
Azilect® is well tolerated in early and advanced Parkinson’s disease patients
Azilect® (rasagiline) is well tolerated with a placebo-like side-effect profile. The most common adverse events with Azilect® (rasagiline) treatment are shown in Table 1.
 Adverse events occurring with an incidence of >5% in the Azilect ® (rasagiline) 1 mg/day group and with a frequency of >2% over placebo ( ref.1) |
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Parkinson's disease is associated with symptoms of hallucinations and confusion. In post marketing experience these symptoms have also been observed in Parkinson's disease patients treated with Azilect
® (rasagiline). Please see
prescribing_information
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Low discontinuation rates due to adverse events - comparable to placebo in monotherapy (
ref.2) and adjunct treatment trials (
ref.3,
ref.4)
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Equally well tolerated in younger and elderly patients(>70 years) (
ref.4)
Please see Summary of Product Characteristics for full prescribing information.
References:
1. Prescribing Information
2. Safety of rasagiline in elderly patients with Parkinson disease
Goetz CG. et al., Neurology 2006; 66(9):1427-9
3. Rasagiline as an adjunct to levodopa in patients with Parkinson's disease and motor fluctuations: a randomised, double-blind, parallel-group trial - The LARGO study
Rascol O. et al. for the LARGO study Group, Lancet 2005; 365:947-954
4. A randomized placebo-controlled trial of rasagiline in levodopa-treated patients with Parkinson disease and motor fluctuations. The PRESTO study
Parkinson Study Group, Arch Neurol 2005; 62:241-248
5. A controlled, randomized, delayed-start study of rasagiline in early Parkinson disease. The TEMPO study (12-month data)
Parkinson Study Group, Arch Neurol 2004; 61:561-566
6. A controlled trial of rasagiline in early Parkinson disease. The TEMPO study (6-month data)
Parkinson Study Group, Arch Neurol 2002; 59:1937-1943
7. Long-Term Efficacy of Rasagiline in Early Parkinson's
Lew MF. et al., Int J Neurosci 2010; 120:404-408
8. A Double-Blind, Delayed-Start Trial of Rasagiline in Parkinson's Disease
Olanow CW. et al., N Engl J Med 2010; 362:657-659
Published: 15/03/2006 Last updated: 10/05/2011