Inbrija (levodopa) vs Nuplazid (pimavanserin)

Inbrija (levodopa) vs Nuplazid (pimavanserin)

Inbrija (levodopa inhalation powder) is specifically designed to treat off episodes in Parkinson's disease, where the effects of oral levodopa wear off before the next dose is due, and is not indicated for the treatment of psychotic symptoms. Nuplazid (pimavanserin) is an atypical antipsychotic approved for the treatment of hallucinations and delusions associated with Parkinson’s disease psychosis and does not treat motor symptoms. When deciding between these medications, it is important to consider the specific symptoms one is aiming to manage: Inbrija for motor fluctuations and Nuplazid for psychosis in the context of Parkinson's disease.

Difference between Inbrija and Nuplazid

Metric Inbrija (levodopa) Nuplazid (pimavanserin)
Generic name Levodopa Pimavanserin
Indications Parkinson's disease motor fluctuations Parkinson's disease psychosis
Mechanism of action Dopamine precursor 5-HT2A receptor inverse agonist
Brand names Inbrija Nuplazid
Administrative route Inhalation Oral
Side effects Nausea, dizziness, cough Peripheral edema, nausea, confused state
Contraindications Non-selective monoamine oxidase (MAO) inhibitors None known
Drug class Dopaminergic antiparkinsonism agents Atypical antipsychotics
Manufacturer Acorda Therapeutics Acadia Pharmaceuticals

Efficacy

Inbrija (Levodopa) for Parkinson's Disease

Inbrija (levodopa inhalation powder) is an inhaled form of levodopa that is used to treat off episodes in people with Parkinson's disease who are already taking carbidopa/levodopa medication. Off episodes are periods when a patient's medications are not working well, causing an increase in Parkinson's symptoms, such as tremors and difficulty moving. Inbrija works by temporarily increasing the level of dopamine in the brain, which helps improve these symptoms. Clinical trials have demonstrated the efficacy of Inbrija in improving motor function during off episodes in Parkinson's disease patients. The medication is designed for use on an as-needed basis and is not intended to replace regular carbidopa/levodopa therapy.

Nuplazid (Pimavanserin) for Parkinson's Disease

Nuplazid (pimavanserin) is an atypical antipsychotic medication that is specifically approved for the treatment of hallucinations and delusions associated with Parkinson's disease psychosis. Unlike traditional antipsychotics, Nuplazid is a selective serotonin inverse agonist and antagonist, preferentially targeting 5-HT2A receptors. This unique mechanism of action is advantageous in Parkinson's disease as it does not worsen the motor symptoms, which is a common side effect of other antipsychotics. Clinical trials have shown that Nuplazid can significantly reduce the frequency and severity of hallucinations and delusions without exacerbating the primary motor symptoms of Parkinson's disease.

Comparative Efficacy in Parkinson's Disease Management

While Inbrija and Nuplazid serve different purposes in the management of Parkinson's disease, both have shown efficacy in their respective roles. Inbrija provides a rapid-acting treatment option to manage motor fluctuations, and Nuplazid addresses the complex neuropsychiatric symptoms such as hallucinations and delusions. It is important to note that these medications are part of a broader treatment regimen and should be used under the guidance of a healthcare professional familiar with the patient's overall health status and progression of Parkinson's disease.

Considerations and Conclusion

Patients and caregivers should be aware that while Inbrija and Nuplazid are effective in managing specific aspects of Parkinson's disease, they may not be suitable for everyone. The decision to use these medications should be based on a thorough medical evaluation and a discussion of potential benefits and risks. Additionally, as with any medication, monitoring for side effects and effectiveness is crucial to ensure optimal treatment outcomes. For those with Parkinson's disease, Inbrija and Nuplazid can offer meaningful improvements in quality of life by addressing some of the challenging symptoms associated with the condition.

Regulatory Agency Approvals

Inbrija
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Nuplazid
  • Food and Drug Administration (FDA), USA

Access Inbrija or Nuplazid today

If Inbrija or Nuplazid are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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