Product image of Madopar (Benserazide Hydrochloride, Levodopa) supplied by GNH India

Madopar

Active Ingredient:
Benserazide Hydrochloride, Levodopa
Origin:
EU

Madopar (Benserazide Hydrochloride, Levodopa)

Levodopa, the active ingredient in Madopar, is a dopamine precursor presented as oral tablets for oral use. It is combined with benserazide hydrochloride to treat Parkinson's disease and Parkinsonian syndrome in adult patients.
GNH India supplies Madopar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Roche Latvija Sia

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Indications & Clinical Uses

Madopar, a dopamine precursor with a decarboxylase inhibitor, is used to manage disorders of the dopaminergic system.

  • Parkinson's disease: improves motor control and reduces rigidity, tremor, and bradykinesia.
  • Parkinsonian syndrome: alleviates secondary Parkinsonism symptoms, enhancing mobility.
  • Motor fluctuations (wearing‑off): helps manage end‑of‑dose deterioration in patients on long‑term therapy.

How It Works

  • Levodopa crosses the blood‑brain barrier and is enzymatically converted to dopamine, restoring deficient central dopaminergic activity. Benserazide inhibits peripheral aromatic L‑amino acid decarboxylase, preventing peripheral conversion of levodopa, thereby increasing its availability to the brain and minimizing peripheral side effects.

Side Effects

Adverse reactions may occur with Madopar and are categorized by frequency.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Vomiting: occasional, often related to rapid dose escalation.
  • Dizziness: may be postural, especially after first doses.
  • Orthostatic hypotension: drop in blood pressure upon standing.
  • Headache: transient, usually resolves with continued therapy.
  • Insomnia: difficulty initiating or maintaining sleep.

Serious or Rare Side Effects

  • Dyskinesia: involuntary movements that can become disabling.
  • Psychiatric disturbances: hallucinations, confusion, or mood changes.
  • Severe hypotension: marked blood pressure reduction requiring medical attention.
  • Cardiac arrhythmias: irregular heart rhythms in susceptible individuals.
  • Neuroleptic malignant syndrome: rare but life‑threatening reaction.

Precautions & Warnings

When prescribing Madopar, clinicians should consider several safety measures.

  • Dose titration: start low and increase gradually to balance efficacy and tolerability.
  • Monitor for dyskinesia: adjust dose if involuntary movements develop.
  • Assess renal and hepatic function: impaired clearance may require dose modification.
  • Avoid abrupt discontinuation: taper to prevent withdrawal and worsening symptoms.
  • Take with food: reduces gastrointestinal irritation.
  • Store at ambient temperature: keep in the original container, protect from moisture.

Avoid Interactions

Madopar may interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Non‑selective MAO inhibitors: risk of hypertensive crisis.
  • High‑dose MAO‑B inhibitors (e.g., selegiline): may increase levodopa plasma levels.
  • Iron or calcium supplements: reduce levodopa absorption.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: additive blood‑pressure lowering effect.
  • SSRIs or SNRIs: potential for serotonin syndrome.
  • High‑protein meals: compete for transport and lower central availability.

Frequently Asked Questions

Madopar is prescribed to manage the motor symptoms of Parkinson's disease and related Parkinsonian syndromes. It helps improve tremor, rigidity, bradykinesia, and overall mobility by restoring dopamine levels in the brain.

Levodopa, the primary component of Madopar, crosses the blood‑brain barrier and is converted into dopamine, the neurotransmitter deficient in Parkinson's disease. Benserazide blocks peripheral conversion, ensuring more levodopa reaches the central nervous system.

The dosage of Madopar is individualized. A qualified prescriber determines the appropriate amount based on the patient’s clinical condition, response, and tolerability, and may adjust the dose over time.

Safety data for Madopar in pregnancy and lactation are limited. The medication should only be used if the potential benefit justifies the potential risk to the fetus or infant, and decisions are made by the treating physician.

To request Madopar, 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.

Madopar combines levodopa with benserazide, offering higher central availability of levodopa compared with levodopa alone. Compared with dopamine agonists, it generally provides stronger symptom control but may have a higher risk of motor complications such as dyskinesia.

Madopar tablets should be stored at ambient temperature, below 25 °C, in the original packaging. Keep them away from moisture and direct sunlight to maintain stability.

Madopar is taken orally, usually with a glass of water. It can be taken with or without food, although taking it with a light meal may reduce gastrointestinal irritation.

Serious risks include the development of dyskinesia, severe orthostatic hypotension, psychiatric disturbances such as hallucinations, and rare events like neuroleptic malignant syndrome. Patients should be monitored regularly for these complications.

Madopar is contraindicated in patients with known hypersensitivity to levodopa, benserazide, or any excipients, and in those taking non‑selective MAO inhibitors. Caution is also advised for individuals with severe cardiovascular disease, narrow‑angle glaucoma, or a history of malignant melanoma.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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