Product image of Nervius (Pramipexole Dihydrochloride Monohydrate) supplied by GNH India

Nervius

Active Ingredient:
Pramipexole Dihydrochloride Monohydrate
Origin:
EU

Nervius (Pramipexole Dihydrochloride Monohydrate)

Pramipexole, the active ingredient in Nervius, is a dopamine agonist presented as an oral tablet for oral use. It stimulates dopaminergic activity in the brain and is employed in the management of Parkinson's disease and restless legs syndrome in adult patients through selective D2/D3 receptor activation to improve motor symptoms and reduce uncomfortable sensations.

GNH India supplies Nervius as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company ensures quality assurance, regulatory compliance and reliable logistics for global distribution.

Manufacturer / TM Owner

Target Pharma Single Member Private Ltd

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Indications & Clinical Uses

  • Pramipexole is a dopamine agonist used in movement‑disorder therapy.
  • Parkinson's disease: improves motor control and reduces rigidity and bradykinesia.
  • Restless legs syndrome: lessens leg discomfort and the urge to move during rest.
  • Parkinson's disease with motor fluctuations: decreases "off" periods and enhances overall daily functioning.

How It Works

  • Pramipexole acts as a selective agonist at dopamine D2 and D3 receptors in the central nervous system. By binding to these receptors, it mimics dopamine’s action, enhancing dopaminergic neurotransmission in basal ganglia circuits that regulate motor activity. This stimulation compensates for the dopamine deficiency characteristic of Parkinson’s disease and modulates sensory pathways implicated in restless legs syndrome, thereby improving motor symptoms and reducing uncomfortable sensations.

Side Effects

Pramipexole may cause a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Somnolence: increased sleepiness or fatigue.
  • Constipation: reduced bowel movements.

Serious or Rare Side Effects

  • Hallucinations: visual or auditory disturbances that may require medical attention.
  • Impulse control disorders: compulsive gambling, shopping, or hypersexuality.
  • Severe hypotension: marked drop in blood pressure leading to fainting.

Precautions & Warnings

When prescribing pramipexole, several precautions should be observed to ensure safe use.

  • Renal function: dose adjustment is required in patients with severe renal impairment.
  • Elderly patients: monitor for orthostatic hypotension and increased sedation.
  • Psychiatric history: watch for emergence of hallucinations or impulse control issues.
  • Concomitant MAO‑B inhibitors: avoid combined use due to risk of excessive dopaminergic stimulation.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk to fetus or infant.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Pramipexole can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Antipsychotics (e.g., haloperidol): may antagonize pramipexole’s effect.
  • Strong CYP2D6 inhibitors (e.g., quinidine): increase pramipexole plasma concentrations.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: additive hypotensive effect may require blood pressure monitoring.
  • Other dopamine agonists: combined use can heighten risk of side effects such as nausea or impulse control disorders.
  • SSRIs or SNRIs: may increase the likelihood of impulse control problems.

Frequently Asked Questions

Nervius contains pramipexole, which is prescribed to manage the motor symptoms of Parkinson's disease and to alleviate the uncomfortable sensations associated with restless legs syndrome in adult patients.

Pramipexole selectively stimulates dopamine D2 and D3 receptors in the brain, enhancing dopaminergic neurotransmission. This compensates for dopamine deficiency in Parkinson's disease and modulates sensory pathways involved in restless legs syndrome, leading to improved motor function and reduced leg discomfort.

The appropriate dose of Nervius is determined individually by a qualified prescriber based on the patient’s condition, response, and tolerability. Dosage adjustments may be needed for renal function, age, or concomitant therapies.

Pramipexole should be used during pregnancy or lactation only if the potential benefit justifies the potential risk to the fetus or infant. Healthcare providers should evaluate the risk‑benefit profile before prescribing to pregnant or nursing women.

To order Nervius, 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.

The primary alternative to pramipexole is ropinirole, another dopamine agonist. Both improve Parkinsonian motor symptoms, but pramipexole has a higher affinity for D3 receptors, which may influence its efficacy in restless legs syndrome. Choice between them depends on individual response, side‑effect profile and physician preference.

Nervius tablets should be stored at ambient temperature, below 25 °C, in the original packaging. Protect them from moisture, direct sunlight and excessive heat to maintain product stability throughout its shelf life.

Nervius is taken orally, usually with a glass of water. It can be administered with or without food, but patients should follow the prescriber’s instructions regarding timing and any dose‑titration schedule.

Serious risks include hallucinations, impulse control disorders such as compulsive gambling or hypersexuality, and severe hypotension that may cause fainting. Patients should report any sudden changes in mood, perception or blood pressure to their healthcare provider promptly.

Nervius is contraindicated in patients with known hypersensitivity to pramipexole or any excipients, and it should be avoided in individuals taking monoamine oxidase‑B inhibitors. Caution is also advised for patients with severe renal impairment, uncontrolled psychiatric illness, or a history of impulse control disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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