Product image of Nalisar (Rasagiline Hemitartrate) supplied by GNH India

Nalisar

Active Ingredient:
Rasagiline Hemitartrate
Origin:
EU

Nalisar (Rasagiline Hemitartrate)

Rasagiline, the active ingredient in Nalisar, is a Monoamine oxidase B (MAO‑B) inhibitor presented as an oral dosage form for oral use. It is indicated for improving motor function and reducing OFF periods in adult patients with Parkinson's disease.

GNH India supplies Nalisar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product conforms to EU quality standards, is manufactured under GMP‑certified conditions, and meets all applicable regulatory requirements for export to more than 50 countries.

Manufacturer / TM Owner

Lanova Farmaceutici S.R.L.

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Indications & Clinical Uses

Rasagiline is a monoamine oxidase B (MAO‑B) inhibitor used in the treatment of Parkinson's disease.

  • Early‑stage Parkinson's disease: helps maintain motor function, reduce tremor severity, and delay progression of motor symptoms.
  • Advanced‑stage Parkinson's disease: reduces OFF periods and improves overall mobility.
  • Adjunct therapy with levodopa: enhances dopaminergic response, allowing lower levodopa doses.
  • Motor fluctuations in Parkinson's disease: stabilizes dopamine levels to smooth symptom control.

How It Works

  • Rasagiline irreversibly binds to the active site of monoamine oxidase B enzymes in the brain, selectively inhibiting their activity. By blocking MAO‑B, the drug prevents dopamine breakdown, leading to increased extracellular dopamine concentrations in the striatum. The elevated dopamine enhances dopaminergic neurotransmission, improving motor control in patients with Parkinson's disease. The inhibition is selective for MAO‑B, sparing MAO‑A, and the effect persists for the lifespan of the enzyme, providing sustained therapeutic benefit.

Side Effects

Rasagiline may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Headache: mild to moderate headache.
  • Nausea: occasional nausea.
  • Dizziness: transient dizziness or light‑headedness.
  • Joint pain: arthralgia.

Serious or Rare Side Effects

  • Hypertensive crisis: severe high blood pressure when combined with tyramine‑rich foods or certain drugs.
  • Serotonin syndrome: risk when used with serotonergic agents, presenting with agitation, fever, and neuromuscular abnormalities.
  • Liver function abnormalities: elevated liver enzymes indicating possible hepatic injury.

Precautions & Warnings

Before initiating rasagiline therapy, consider the following precautions and warnings.

  • Assess cardiovascular status: monitor blood pressure, especially if the patient consumes tyramine‑rich foods.
  • Review psychiatric history: avoid use in patients with uncontrolled depression or psychosis.
  • Evaluate concomitant serotonergic drugs: consider risk of serotonin syndrome.
  • Adjust levodopa dosing: monitor for dyskinesia when rasagiline is added.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and light.

Avoid Interactions

Rasagiline can interact with several medicines; interactions are classified by their clinical significance.

Major Interactions (Avoid)

  • Meperidine or other opioid analgesics: may precipitate severe hypotension or serotonin syndrome.
  • Selective serotonin reuptake inhibitors (SSRIs) and other serotonergic agents: increase risk of serotonin syndrome.
  • Tyramine‑rich foods combined with non‑selective MAO inhibitors: can cause hypertensive crisis.

Moderate Interactions (Monitor Closely)

  • Levodopa/carbidopa: may enhance dopaminergic effects, requiring dose adjustment.
  • Sympathomimetic drugs (e.g., epinephrine): may augment pressor response.
  • Antihypertensive agents: monitor for additive blood pressure lowering.

Frequently Asked Questions

Nalisar contains rasagiline, which is prescribed to manage the motor symptoms of Parkinson's disease. It helps improve movement, reduce tremor, and lessen the duration of OFF periods in patients receiving levodopa therapy.

Rasagiline selectively and irreversibly inhibits the enzyme monoamine oxidase B (MAO‑B) in the brain. This inhibition prevents the breakdown of dopamine, increasing its extracellular concentration and enhancing dopaminergic neurotransmission, which improves motor control in Parkinson's disease.

The dosage of Nalisar is determined by the prescribing clinician based on the individual patient's condition, response, and concomitant therapies. Physicians typically start with a low dose and may adjust it according to therapeutic effect and tolerability.

Limited clinical data are available on rasagiline use in pregnancy or lactation. Because potential risks cannot be ruled out, the drug is generally avoided unless the expected benefit justifies the potential hazard to the fetus or infant.

To request Nalisar, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Nalisar (rasagiline) and selegiline are both selective MAO‑B inhibitors used for Parkinson's disease. Rasagiline has a longer half‑life, does not require dietary tyramine restrictions, and is associated with a lower incidence of certain side effects, making it a convenient alternative for many patients.

Store Nalisar at ambient temperature, preferably below 25 °C. Keep the product in its original container, protect it from moisture and direct light, and avoid exposing it to extreme temperatures or humidity to maintain potency.

Nalisar is taken orally. The tablet should be swallowed whole with a glass of water, preferably at the same time each day. It may be taken with or without food, as directed by the prescribing healthcare professional.

Serious risks include hypertensive crisis when combined with tyramine‑rich foods or non‑selective MAO inhibitors, serotonin syndrome if used with serotonergic drugs, and potential liver enzyme elevations indicating hepatic injury. Patients should be monitored closely for these events.

Nalisar should be avoided in patients currently taking non‑selective MAO inhibitors, certain opioid analgesics such as meperidine, or serotonergic agents that could precipitate serotonin syndrome. It is also contraindicated in individuals with known hypersensitivity to rasagiline or any excipients in the formulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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