What is the risk of Parkinsonism associated with Mirtazapine (Remeron)?

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Last updated: May 20, 2025View editorial policy

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From the Research

Mirtazapine is generally considered to have a low risk of causing or worsening Parkinson's disease symptoms compared to other antidepressants, and it can be a preferred choice for patients with Parkinson's disease or those at risk for parkinsonism. This is due to its unique mechanism of action as an alpha-2 antagonist and 5-HT2/5-HT3 receptor antagonist, which doesn't significantly interfere with dopaminergic neurotransmission that is already deficient in Parkinson's disease 1. The typical starting dose is 7.5-15 mg at bedtime, which can be gradually increased to 30-45 mg if needed.

Key Points to Consider

  • Mirtazapine's sedating effects at lower doses (15 mg or less) can help with sleep disturbances common in Parkinson's patients, while higher doses tend to be more activating 2.
  • Patients should be monitored for potential side effects including sedation, increased appetite, weight gain, and dry mouth 1.
  • If parkinsonism symptoms worsen after starting mirtazapine, which is uncommon but possible, the medication should be reevaluated 3.
  • There is evidence to suggest that mirtazapine may be effective in alleviating PD psychosis and reducing dyskinesia without hindering L-DOPA anti-parkinsonian action 4.

Management and Treatment

  • Mirtazapine can be considered as a treatment option for patients with Parkinson's disease or those at risk for parkinsonism who require antidepressant therapy 1.
  • The medication's potential benefits in reducing psychosis and improving sleep disturbances should be weighed against its potential risks and side effects 2, 3.
  • Further research is needed to fully understand the therapeutic effects of mirtazapine in Parkinson's disease and to determine its optimal dosage and treatment duration 4, 1.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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